dbSNP Short Genetic Variations
Welcome to the Reference SNP (rs) Report
All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.
Reference SNP (rs) Report
This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.
rs1472894593
Current Build 156
Released September 21, 2022
- Organism
- Homo sapiens
- Position
-
chr18:37273152 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
- Alleles
- C>T
- Variation Type
- SNV Single Nucleotide Variation
- Frequency
- T=0.000004 (1/249948, GnomAD_exome)
- Clinical Significance
- Not Reported in ClinVar
- Gene : Consequence
-
CELF4 : Synonymous VariantLOC105372068 : 2KB Upstream Variant
- Publications
- 0 citations
- Genomic View
- See rs on genome
Help
Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").
Download| Study | Population | Group | Sample Size | Ref Allele | Alt Allele |
|---|---|---|---|---|---|
| gnomAD - Exomes | Global | Study-wide | 249948 | C=0.999996 | T=0.000004 |
| gnomAD - Exomes | European | Sub | 134238 | C=0.999993 | T=0.000007 |
| gnomAD - Exomes | Asian | Sub | 48924 | C=1.00000 | T=0.00000 |
| gnomAD - Exomes | American | Sub | 34480 | C=1.00000 | T=0.00000 |
| gnomAD - Exomes | African | Sub | 16186 | C=1.00000 | T=0.00000 |
| gnomAD - Exomes | Ashkenazi Jewish | Sub | 10014 | C=1.00000 | T=0.00000 |
| gnomAD - Exomes | Other | Sub | 6106 | C=1.0000 | T=0.0000 |
Help
Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.
Genomic Placements
| Sequence name | Change |
|---|---|
| GRCh38.p14 chr 18 | NC_000018.10:g.37273152C>T |
| GRCh37.p13 chr 18 | NC_000018.9:g.34853115C>T |
Gene: CELF4, CUGBP Elav-like family member 4
(minus strand)
| Molecule type | Change | Amino acid[Codon] | SO Term |
|---|---|---|---|
| CELF4 transcript variant 71 | NM_001353701.2:c. | N/A | Genic Downstream Transcript Variant |
| CELF4 transcript variant 1 | NM_020180.4:c.813G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 1 | NP_064565.1:p.Gln271= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 22 | NM_001353705.2:c.777G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 22 | NP_001340634.1:p.Gln259= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 40 | NM_001353755.2:c.777G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 40 | NP_001340684.1:p.Gln259= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 5 | NM_001330603.2:c.810G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 5 | NP_001317532.1:p.Gln270= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 46 | NM_001353723.2:c.810G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 46 | NP_001340652.1:p.Gln270= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 51 | NM_001353747.2:c.810G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 51 | NP_001340676.1:p.Gln270= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 30 | NM_001353718.2:c.810G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 30 | NP_001340647.1:p.Gln270= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 48 | NM_001353729.2:c.810G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 48 | NP_001340658.1:p.Gln270= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 45 | NM_001353696.2:c.810G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 45 | NP_001340625.1:p.Gln270= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 10 | NM_001353746.2:c.810G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 10 | NP_001340675.1:p.Gln270= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 67 | NM_001353759.2:c.411G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 67 | NP_001340688.1:p.Gln137= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 63 | NM_001353732.2:c.780G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 63 | NP_001340661.1:p.Gln260= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 28 | NM_001353745.2:c.810G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 28 | NP_001340674.1:p.Gln270= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 27 | NM_001353738.2:c.810G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 27 | NP_001340667.1:p.Gln270= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 38 | NM_001353750.2:c.780G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 38 | NP_001340679.1:p.Gln260= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 33 | NM_001353748.2:c.783G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 33 | NP_001340677.1:p.Gln261= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 32 | NM_001353709.2:c.780G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 32 | NP_001340638.1:p.Gln260= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 21 | NM_001353707.2:c.780G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 21 | NP_001340636.1:p.Gln260= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 9 | NM_001353731.2:c.813G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 9 | NP_001340660.1:p.Gln271= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 37 | NM_001353721.2:c.780G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 37 | NP_001340650.1:p.Gln260= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 16 | NM_001353728.2:c.780G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 16 | NP_001340657.1:p.Gln260= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 36 | NM_001353710.2:c.783G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 36 | NP_001340639.1:p.Gln261= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 19 | NM_001353715.2:c.783G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 19 | NP_001340644.1:p.Gln261= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 6 | NM_001353740.2:c.813G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 6 | NP_001340669.1:p.Gln271= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 20 | NM_001353717.2:c.783G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 20 | NP_001340646.1:p.Gln261= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 2 | NM_001025087.2:c.810G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 2 | NP_001020258.1:p.Gln270= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 14 | NM_001353726.2:c.780G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 14 | NP_001340655.1:p.Gln260= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 34 | NM_001353752.2:c.780G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 34 | NP_001340681.1:p.Gln260= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 43 | NM_001353725.2:c.777G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 43 | NP_001340654.1:p.Gln259= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 68 | NM_001353760.2:c.414G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 68 | NP_001340689.1:p.Gln138= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 24 | NM_001353744.2:c.813G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 24 | NP_001340673.1:p.Gln271= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 7 | NM_001353749.2:c.810G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 7 | NP_001340678.1:p.Gln270= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 18 | NM_001353742.2:c.810G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 18 | NP_001340671.1:p.Gln270= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 57 | NM_001353713.2:c.780G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 57 | NP_001340642.1:p.Gln260= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 44 | NM_001353708.2:c.813G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 44 | NP_001340637.1:p.Gln271= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 56 | NM_001353700.2:c.783G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 56 | NP_001340629.1:p.Gln261= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 42 | NM_001353714.2:c.780G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 42 | NP_001340643.1:p.Gln260= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 3 | NM_001025088.2:c.807G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 3 | NP_001020259.1:p.Gln269= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 26 | NM_001353724.2:c.813G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 26 | NP_001340653.1:p.Gln271= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 8 | NM_001353734.2:c.813G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 8 | NP_001340663.1:p.Gln271= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 23 | NM_001353698.2:c.810G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 23 | NP_001340627.1:p.Gln270= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 64 | NM_001353722.2:c.777G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 64 | NP_001340651.1:p.Gln259= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 54 | NM_001353737.2:c.810G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 54 | NP_001340666.1:p.Gln270= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 11 | NM_001353735.2:c.780G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 11 | NP_001340664.1:p.Gln260= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 55 | NM_001353697.2:c.780G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 55 | NP_001340626.1:p.Gln260= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 60 | NM_001353706.2:c.777G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 60 | NP_001340635.1:p.Gln259= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 17 | NM_001353739.2:c.777G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 17 | NP_001340668.1:p.Gln259= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 41 | NM_001353711.2:c.777G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 41 | NP_001340640.1:p.Gln259= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 29 | NM_001353702.2:c.807G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 29 | NP_001340631.1:p.Gln269= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 35 | NM_001353695.2:c.780G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 35 | NP_001340624.1:p.Gln260= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 39 | NM_001353753.2:c.780G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 39 | NP_001340682.1:p.Gln260= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 15 | NM_001353741.2:c.780G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 15 | NP_001340670.1:p.Gln260= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 4 | NM_001025089.2:c.783G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 4 | NP_001020260.1:p.Gln261= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 52 | NM_001353754.2:c.807G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 52 | NP_001340683.1:p.Gln269= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 12 | NM_001353733.2:c.777G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 12 | NP_001340662.1:p.Gln259= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 66 | NM_001353761.2:c.441G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 66 | NP_001340690.1:p.Gln147= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 70 | NM_001353758.2:c.411G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 70 | NP_001340687.1:p.Gln137= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 13 | NM_001353703.2:c.783G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 13 | NP_001340632.1:p.Gln261= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 65 | NM_001353756.2:c.441G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 65 | NP_001340685.1:p.Gln147= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 47 | NM_001353743.2:c.813G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 47 | NP_001340672.1:p.Gln271= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 62 | NM_001353727.2:c.780G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 62 | NP_001340656.1:p.Gln260= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 25 | NM_001353751.2:c.813G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 25 | NP_001340680.1:p.Gln271= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 69 | NM_001353757.2:c.414G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 69 | NP_001340686.1:p.Gln138= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 61 | NM_001353720.2:c.783G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 61 | NP_001340649.1:p.Gln261= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 50 | NM_001353736.2:c.813G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 50 | NP_001340665.1:p.Gln271= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 58 | NM_001353719.2:c.783G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 58 | NP_001340648.1:p.Gln261= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 59 | NM_001353699.2:c.780G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 59 | NP_001340628.1:p.Gln260= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 49 | NM_001353730.2:c.810G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 49 | NP_001340659.1:p.Gln270= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 31 | NM_001353712.2:c.807G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 31 | NP_001340641.1:p.Gln269= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 53 | NM_001353716.2:c.807G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform 53 | NP_001340645.1:p.Gln269= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant 79 | NR_148525.2:n.937G>A | N/A | Non Coding Transcript Variant |
| CELF4 transcript variant 74 | NR_148520.2:n.967G>A | N/A | Non Coding Transcript Variant |
| CELF4 transcript variant 80 | NR_148526.2:n.967G>A | N/A | Non Coding Transcript Variant |
| CELF4 transcript variant 76 | NR_148522.2:n.934G>A | N/A | Non Coding Transcript Variant |
| CELF4 transcript variant 75 | NR_148521.2:n.970G>A | N/A | Non Coding Transcript Variant |
| CELF4 transcript variant 78 | NR_148524.2:n.937G>A | N/A | Non Coding Transcript Variant |
| CELF4 transcript variant 82 | NR_148528.2:n.967G>A | N/A | Non Coding Transcript Variant |
| CELF4 transcript variant 73 | NR_148519.2:n.934G>A | N/A | Non Coding Transcript Variant |
| CELF4 transcript variant 72 | NR_148518.2:n.937G>A | N/A | Non Coding Transcript Variant |
| CELF4 transcript variant 81 | NR_148527.2:n.970G>A | N/A | Non Coding Transcript Variant |
| CELF4 transcript variant 77 | NR_148523.2:n.940G>A | N/A | Non Coding Transcript Variant |
| CELF4 transcript variant X1 | XM_047437628.1:c.813G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X1 | XP_047293584.1:p.Gln271= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X2 | XM_047437629.1:c.810G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X2 | XP_047293585.1:p.Gln270= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X3 | XM_047437630.1:c.783G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X3 | XP_047293586.1:p.Gln261= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X4 | XM_047437631.1:c.783G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X4 | XP_047293587.1:p.Gln261= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X5 | XM_047437632.1:c.813G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X5 | XP_047293588.1:p.Gln271= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X6 | XM_047437633.1:c.813G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X6 | XP_047293589.1:p.Gln271= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X7 | XM_047437634.1:c.810G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X7 | XP_047293590.1:p.Gln270= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X8 | XM_047437635.1:c.813G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X8 | XP_047293591.1:p.Gln271= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X9 | XM_047437636.1:c.783G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X9 | XP_047293592.1:p.Gln261= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X10 | XM_047437637.1:c.780G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X10 | XP_047293593.1:p.Gln260= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X11 | XM_047437638.1:c.783G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X11 | XP_047293594.1:p.Gln261= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X12 | XM_047437639.1:c.813G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X12 | XP_047293595.1:p.Gln271= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X13 | XM_047437640.1:c.810G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X13 | XP_047293596.1:p.Gln270= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X14 | XM_047437641.1:c.813G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X14 | XP_047293597.1:p.Gln271= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X15 | XM_047437642.1:c.813G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X15 | XP_047293598.1:p.Gln271= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X16 | XM_047437643.1:c.810G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X16 | XP_047293599.1:p.Gln270= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X17 | XM_047437644.1:c.810G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X17 | XP_047293600.1:p.Gln270= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X18 | XM_047437645.1:c.813G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X18 | XP_047293601.1:p.Gln271= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X19 | XM_047437646.1:c.810G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X19 | XP_047293602.1:p.Gln270= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X20 | XM_047437647.1:c.780G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X20 | XP_047293603.1:p.Gln260= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X21 | XM_047437648.1:c.783G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X21 | XP_047293604.1:p.Gln261= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X22 | XM_047437649.1:c.780G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X22 | XP_047293605.1:p.Gln260= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X23 | XM_047437650.1:c.780G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X23 | XP_047293606.1:p.Gln260= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X24 | XM_047437651.1:c.783G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X24 | XP_047293607.1:p.Gln261= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X25 | XM_047437652.1:c.780G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X25 | XP_047293608.1:p.Gln260= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X26 | XM_047437653.1:c.783G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X26 | XP_047293609.1:p.Gln261= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X27 | XM_047437654.1:c.813G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X27 | XP_047293610.1:p.Gln271= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X28 | XM_047437655.1:c.810G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X28 | XP_047293611.1:p.Gln270= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X29 | XM_047437656.1:c.813G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X29 | XP_047293612.1:p.Gln271= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X30 | XM_047437657.1:c.813G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X30 | XP_047293613.1:p.Gln271= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X31 | XM_047437658.1:c.810G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X31 | XP_047293614.1:p.Gln270= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X32 | XM_047437659.1:c.810G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X32 | XP_047293615.1:p.Gln270= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X33 | XM_047437660.1:c.813G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X33 | XP_047293616.1:p.Gln271= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X34 | XM_047437661.1:c.810G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X34 | XP_047293617.1:p.Gln270= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X35 | XM_047437662.1:c.783G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X35 | XP_047293618.1:p.Gln261= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X36 | XM_047437663.1:c.780G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X36 | XP_047293619.1:p.Gln260= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X37 | XM_047437664.1:c.783G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X37 | XP_047293620.1:p.Gln261= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X38 | XM_047437665.1:c.783G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X38 | XP_047293621.1:p.Gln261= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X39 | XM_047437666.1:c.780G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X39 | XP_047293622.1:p.Gln260= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X40 | XM_047437667.1:c.780G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X40 | XP_047293623.1:p.Gln260= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X41 | XM_047437668.1:c.783G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X41 | XP_047293624.1:p.Gln261= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X42 | XM_047437669.1:c.780G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X42 | XP_047293625.1:p.Gln260= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X43 | XM_047437670.1:c.783G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X43 | XP_047293626.1:p.Gln261= | Q (Gln) > Q (Gln) | Synonymous Variant |
| CELF4 transcript variant X44 | XM_047437671.1:c.780G>A | Q [CAG] > Q [CAA] | Coding Sequence Variant |
| CUGBP Elav-like family member 4 isoform X44 | XP_047293627.1:p.Gln260= | Q (Gln) > Q (Gln) | Synonymous Variant |
Gene: LOC105372068, uncharacterized LOC105372068
(plus strand)
:
2KB Upstream Variant
| Molecule type | Change | Amino acid[Codon] | SO Term |
|---|---|---|---|
| LOC105372068 transcript | NR_134588.1:n. | N/A | Upstream Transcript Variant |
Help
Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.
Not Reported in ClinVar
Help
Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".
| Placement | C= | T |
|---|---|---|
| GRCh38.p14 chr 18 | NC_000018.10:g.37273152= | NC_000018.10:g.37273152C>T |
| GRCh37.p13 chr 18 | NC_000018.9:g.34853115= | NC_000018.9:g.34853115C>T |
| CELF4 transcript variant 1 | NM_020180.4:c.813= | NM_020180.4:c.813G>A |
| CELF4 transcript variant 1 | NM_020180.3:c.813= | NM_020180.3:c.813G>A |
| CELF4 transcript variant 6 | NM_001353740.2:c.813= | NM_001353740.2:c.813G>A |
| CELF4 transcript variant 6 | NM_001353740.1:c.813= | NM_001353740.1:c.813G>A |
| CELF4 transcript variant 7 | NM_001353749.2:c.810= | NM_001353749.2:c.810G>A |
| CELF4 transcript variant 7 | NM_001353749.1:c.810= | NM_001353749.1:c.810G>A |
| CELF4 transcript variant 11 | NM_001353735.2:c.780= | NM_001353735.2:c.780G>A |
| CELF4 transcript variant 11 | NM_001353735.1:c.780= | NM_001353735.1:c.780G>A |
| CELF4 transcript variant 12 | NM_001353733.2:c.777= | NM_001353733.2:c.777G>A |
| CELF4 transcript variant 12 | NM_001353733.1:c.777= | NM_001353733.1:c.777G>A |
| CELF4 transcript variant 81 | NR_148527.2:n.970= | NR_148527.2:n.970G>A |
| CELF4 transcript variant 81 | NR_148527.1:n.1209= | NR_148527.1:n.1209G>A |
| CELF4 transcript variant 82 | NR_148528.2:n.967= | NR_148528.2:n.967G>A |
| CELF4 transcript variant 82 | NR_148528.1:n.1206= | NR_148528.1:n.1206G>A |
| CELF4 transcript variant 80 | NR_148526.2:n.967= | NR_148526.2:n.967G>A |
| CELF4 transcript variant 80 | NR_148526.1:n.1206= | NR_148526.1:n.1206G>A |
| CELF4 transcript variant 75 | NR_148521.2:n.970= | NR_148521.2:n.970G>A |
| CELF4 transcript variant 75 | NR_148521.1:n.1209= | NR_148521.1:n.1209G>A |
| CELF4 transcript variant 74 | NR_148520.2:n.967= | NR_148520.2:n.967G>A |
| CELF4 transcript variant 74 | NR_148520.1:n.1206= | NR_148520.1:n.1206G>A |
| CELF4 transcript variant 8 | NM_001353734.2:c.813= | NM_001353734.2:c.813G>A |
| CELF4 transcript variant 8 | NM_001353734.1:c.813= | NM_001353734.1:c.813G>A |
| CELF4 transcript variant 10 | NM_001353746.2:c.810= | NM_001353746.2:c.810G>A |
| CELF4 transcript variant 10 | NM_001353746.1:c.810= | NM_001353746.1:c.810G>A |
| CELF4 transcript variant 9 | NM_001353731.2:c.813= | NM_001353731.2:c.813G>A |
| CELF4 transcript variant 9 | NM_001353731.1:c.813= | NM_001353731.1:c.813G>A |
| CELF4 transcript variant 77 | NR_148523.2:n.940= | NR_148523.2:n.940G>A |
| CELF4 transcript variant 77 | NR_148523.1:n.1179= | NR_148523.1:n.1179G>A |
| CELF4 transcript variant 18 | NM_001353742.2:c.810= | NM_001353742.2:c.810G>A |
| CELF4 transcript variant 18 | NM_001353742.1:c.810= | NM_001353742.1:c.810G>A |
| CELF4 transcript variant 79 | NR_148525.2:n.937= | NR_148525.2:n.937G>A |
| CELF4 transcript variant 79 | NR_148525.1:n.1176= | NR_148525.1:n.1176G>A |
| CELF4 transcript variant 78 | NR_148524.2:n.937= | NR_148524.2:n.937G>A |
| CELF4 transcript variant 78 | NR_148524.1:n.1176= | NR_148524.1:n.1176G>A |
| CELF4 transcript variant 76 | NR_148522.2:n.934= | NR_148522.2:n.934G>A |
| CELF4 transcript variant 76 | NR_148522.1:n.1173= | NR_148522.1:n.1173G>A |
| CELF4 transcript variant 13 | NM_001353703.2:c.783= | NM_001353703.2:c.783G>A |
| CELF4 transcript variant 13 | NM_001353703.1:c.783= | NM_001353703.1:c.783G>A |
| CELF4 transcript variant 15 | NM_001353741.2:c.780= | NM_001353741.2:c.780G>A |
| CELF4 transcript variant 15 | NM_001353741.1:c.780= | NM_001353741.1:c.780G>A |
| CELF4 transcript variant 14 | NM_001353726.2:c.780= | NM_001353726.2:c.780G>A |
| CELF4 transcript variant 14 | NM_001353726.1:c.780= | NM_001353726.1:c.780G>A |
| CELF4 transcript variant 16 | NM_001353728.2:c.780= | NM_001353728.2:c.780G>A |
| CELF4 transcript variant 16 | NM_001353728.1:c.780= | NM_001353728.1:c.780G>A |
| CELF4 transcript variant 17 | NM_001353739.2:c.777= | NM_001353739.2:c.777G>A |
| CELF4 transcript variant 17 | NM_001353739.1:c.777= | NM_001353739.1:c.777G>A |
| CELF4 transcript variant 20 | NM_001353717.2:c.783= | NM_001353717.2:c.783G>A |
| CELF4 transcript variant 20 | NM_001353717.1:c.783= | NM_001353717.1:c.783G>A |
| CELF4 transcript variant 21 | NM_001353707.2:c.780= | NM_001353707.2:c.780G>A |
| CELF4 transcript variant 21 | NM_001353707.1:c.780= | NM_001353707.1:c.780G>A |
| CELF4 transcript variant 22 | NM_001353705.2:c.777= | NM_001353705.2:c.777G>A |
| CELF4 transcript variant 22 | NM_001353705.1:c.777= | NM_001353705.1:c.777G>A |
| CELF4 transcript variant 25 | NM_001353751.2:c.813= | NM_001353751.2:c.813G>A |
| CELF4 transcript variant 25 | NM_001353751.1:c.813= | NM_001353751.1:c.813G>A |
| CELF4 transcript variant 24 | NM_001353744.2:c.813= | NM_001353744.2:c.813G>A |
| CELF4 transcript variant 24 | NM_001353744.1:c.813= | NM_001353744.1:c.813G>A |
| CELF4 transcript variant 23 | NM_001353698.2:c.810= | NM_001353698.2:c.810G>A |
| CELF4 transcript variant 23 | NM_001353698.1:c.810= | NM_001353698.1:c.810G>A |
| CELF4 transcript variant 2 | NM_001025087.2:c.810= | NM_001025087.2:c.810G>A |
| CELF4 transcript variant 2 | NM_001025087.1:c.810= | NM_001025087.1:c.810G>A |
| CELF4 transcript variant 28 | NM_001353745.2:c.810= | NM_001353745.2:c.810G>A |
| CELF4 transcript variant 28 | NM_001353745.1:c.810= | NM_001353745.1:c.810G>A |
| CELF4 transcript variant 27 | NM_001353738.2:c.810= | NM_001353738.2:c.810G>A |
| CELF4 transcript variant 27 | NM_001353738.1:c.810= | NM_001353738.1:c.810G>A |
| CELF4 transcript variant 26 | NM_001353724.2:c.813= | NM_001353724.2:c.813G>A |
| CELF4 transcript variant 26 | NM_001353724.1:c.813= | NM_001353724.1:c.813G>A |
| CELF4 transcript variant 5 | NM_001330603.2:c.810= | NM_001330603.2:c.810G>A |
| CELF4 transcript variant 5 | NM_001330603.1:c.810= | NM_001330603.1:c.810G>A |
| CELF4 transcript variant 3 | NM_001025088.2:c.807= | NM_001025088.2:c.807G>A |
| CELF4 transcript variant 3 | NM_001025088.1:c.807= | NM_001025088.1:c.807G>A |
| CELF4 transcript variant 30 | NM_001353718.2:c.810= | NM_001353718.2:c.810G>A |
| CELF4 transcript variant 30 | NM_001353718.1:c.810= | NM_001353718.1:c.810G>A |
| CELF4 transcript variant 29 | NM_001353702.2:c.807= | NM_001353702.2:c.807G>A |
| CELF4 transcript variant 29 | NM_001353702.1:c.807= | NM_001353702.1:c.807G>A |
| CELF4 transcript variant 31 | NM_001353712.2:c.807= | NM_001353712.2:c.807G>A |
| CELF4 transcript variant 31 | NM_001353712.1:c.807= | NM_001353712.1:c.807G>A |
| CELF4 transcript variant 72 | NR_148518.2:n.937= | NR_148518.2:n.937G>A |
| CELF4 transcript variant 72 | NR_148518.1:n.1176= | NR_148518.1:n.1176G>A |
| CELF4 transcript variant 34 | NM_001353752.2:c.780= | NM_001353752.2:c.780G>A |
| CELF4 transcript variant 34 | NM_001353752.1:c.780= | NM_001353752.1:c.780G>A |
| CELF4 transcript variant 33 | NM_001353748.2:c.783= | NM_001353748.2:c.783G>A |
| CELF4 transcript variant 33 | NM_001353748.1:c.783= | NM_001353748.1:c.783G>A |
| CELF4 transcript variant 32 | NM_001353709.2:c.780= | NM_001353709.2:c.780G>A |
| CELF4 transcript variant 32 | NM_001353709.1:c.780= | NM_001353709.1:c.780G>A |
| CELF4 transcript variant 73 | NR_148519.2:n.934= | NR_148519.2:n.934G>A |
| CELF4 transcript variant 73 | NR_148519.1:n.1173= | NR_148519.1:n.1173G>A |
| CELF4 transcript variant 19 | NM_001353715.2:c.783= | NM_001353715.2:c.783G>A |
| CELF4 transcript variant 19 | NM_001353715.1:c.783= | NM_001353715.1:c.783G>A |
| CELF4 transcript variant 40 | NM_001353755.2:c.777= | NM_001353755.2:c.777G>A |
| CELF4 transcript variant 40 | NM_001353755.1:c.777= | NM_001353755.1:c.777G>A |
| CELF4 transcript variant 39 | NM_001353753.2:c.780= | NM_001353753.2:c.780G>A |
| CELF4 transcript variant 39 | NM_001353753.1:c.780= | NM_001353753.1:c.780G>A |
| CELF4 transcript variant 38 | NM_001353750.2:c.780= | NM_001353750.2:c.780G>A |
| CELF4 transcript variant 38 | NM_001353750.1:c.780= | NM_001353750.1:c.780G>A |
| CELF4 transcript variant 37 | NM_001353721.2:c.780= | NM_001353721.2:c.780G>A |
| CELF4 transcript variant 37 | NM_001353721.1:c.780= | NM_001353721.1:c.780G>A |
| CELF4 transcript variant 36 | NM_001353710.2:c.783= | NM_001353710.2:c.783G>A |
| CELF4 transcript variant 36 | NM_001353710.1:c.783= | NM_001353710.1:c.783G>A |
| CELF4 transcript variant 35 | NM_001353695.2:c.780= | NM_001353695.2:c.780G>A |
| CELF4 transcript variant 35 | NM_001353695.1:c.780= | NM_001353695.1:c.780G>A |
| CELF4 transcript variant 43 | NM_001353725.2:c.777= | NM_001353725.2:c.777G>A |
| CELF4 transcript variant 43 | NM_001353725.1:c.777= | NM_001353725.1:c.777G>A |
| CELF4 transcript variant 42 | NM_001353714.2:c.780= | NM_001353714.2:c.780G>A |
| CELF4 transcript variant 42 | NM_001353714.1:c.780= | NM_001353714.1:c.780G>A |
| CELF4 transcript variant 41 | NM_001353711.2:c.777= | NM_001353711.2:c.777G>A |
| CELF4 transcript variant 41 | NM_001353711.1:c.777= | NM_001353711.1:c.777G>A |
| CELF4 transcript variant 44 | NM_001353708.2:c.813= | NM_001353708.2:c.813G>A |
| CELF4 transcript variant 44 | NM_001353708.1:c.813= | NM_001353708.1:c.813G>A |
| CELF4 transcript variant 47 | NM_001353743.2:c.813= | NM_001353743.2:c.813G>A |
| CELF4 transcript variant 47 | NM_001353743.1:c.813= | NM_001353743.1:c.813G>A |
| CELF4 transcript variant 46 | NM_001353723.2:c.810= | NM_001353723.2:c.810G>A |
| CELF4 transcript variant 46 | NM_001353723.1:c.810= | NM_001353723.1:c.810G>A |
| CELF4 transcript variant 45 | NM_001353696.2:c.810= | NM_001353696.2:c.810G>A |
| CELF4 transcript variant 45 | NM_001353696.1:c.810= | NM_001353696.1:c.810G>A |
| CELF4 transcript variant 52 | NM_001353754.2:c.807= | NM_001353754.2:c.807G>A |
| CELF4 transcript variant 52 | NM_001353754.1:c.807= | NM_001353754.1:c.807G>A |
| CELF4 transcript variant 51 | NM_001353747.2:c.810= | NM_001353747.2:c.810G>A |
| CELF4 transcript variant 51 | NM_001353747.1:c.810= | NM_001353747.1:c.810G>A |
| CELF4 transcript variant 50 | NM_001353736.2:c.813= | NM_001353736.2:c.813G>A |
| CELF4 transcript variant 50 | NM_001353736.1:c.813= | NM_001353736.1:c.813G>A |
| CELF4 transcript variant 49 | NM_001353730.2:c.810= | NM_001353730.2:c.810G>A |
| CELF4 transcript variant 49 | NM_001353730.1:c.810= | NM_001353730.1:c.810G>A |
| CELF4 transcript variant 48 | NM_001353729.2:c.810= | NM_001353729.2:c.810G>A |
| CELF4 transcript variant 48 | NM_001353729.1:c.810= | NM_001353729.1:c.810G>A |
| CELF4 transcript variant 54 | NM_001353737.2:c.810= | NM_001353737.2:c.810G>A |
| CELF4 transcript variant 54 | NM_001353737.1:c.810= | NM_001353737.1:c.810G>A |
| CELF4 transcript variant 53 | NM_001353716.2:c.807= | NM_001353716.2:c.807G>A |
| CELF4 transcript variant 53 | NM_001353716.1:c.807= | NM_001353716.1:c.807G>A |
| CELF4 transcript variant 4 | NM_001025089.2:c.783= | NM_001025089.2:c.783G>A |
| CELF4 transcript variant 4 | NM_001025089.1:c.783= | NM_001025089.1:c.783G>A |
| CELF4 transcript variant 58 | NM_001353719.2:c.783= | NM_001353719.2:c.783G>A |
| CELF4 transcript variant 58 | NM_001353719.1:c.783= | NM_001353719.1:c.783G>A |
| CELF4 transcript variant 57 | NM_001353713.2:c.780= | NM_001353713.2:c.780G>A |
| CELF4 transcript variant 57 | NM_001353713.1:c.780= | NM_001353713.1:c.780G>A |
| CELF4 transcript variant 56 | NM_001353700.2:c.783= | NM_001353700.2:c.783G>A |
| CELF4 transcript variant 56 | NM_001353700.1:c.783= | NM_001353700.1:c.783G>A |
| CELF4 transcript variant 55 | NM_001353697.2:c.780= | NM_001353697.2:c.780G>A |
| CELF4 transcript variant 55 | NM_001353697.1:c.780= | NM_001353697.1:c.780G>A |
| CELF4 transcript variant 63 | NM_001353732.2:c.780= | NM_001353732.2:c.780G>A |
| CELF4 transcript variant 63 | NM_001353732.1:c.780= | NM_001353732.1:c.780G>A |
| CELF4 transcript variant 62 | NM_001353727.2:c.780= | NM_001353727.2:c.780G>A |
| CELF4 transcript variant 62 | NM_001353727.1:c.780= | NM_001353727.1:c.780G>A |
| CELF4 transcript variant 61 | NM_001353720.2:c.783= | NM_001353720.2:c.783G>A |
| CELF4 transcript variant 61 | NM_001353720.1:c.783= | NM_001353720.1:c.783G>A |
| CELF4 transcript variant 60 | NM_001353706.2:c.777= | NM_001353706.2:c.777G>A |
| CELF4 transcript variant 60 | NM_001353706.1:c.777= | NM_001353706.1:c.777G>A |
| CELF4 transcript variant 59 | NM_001353699.2:c.780= | NM_001353699.2:c.780G>A |
| CELF4 transcript variant 59 | NM_001353699.1:c.780= | NM_001353699.1:c.780G>A |
| CELF4 transcript variant 64 | NM_001353722.2:c.777= | NM_001353722.2:c.777G>A |
| CELF4 transcript variant 64 | NM_001353722.1:c.777= | NM_001353722.1:c.777G>A |
| CELF4 transcript variant 65 | NM_001353756.2:c.441= | NM_001353756.2:c.441G>A |
| CELF4 transcript variant 65 | NM_001353756.1:c.441= | NM_001353756.1:c.441G>A |
| CELF4 transcript variant 66 | NM_001353761.2:c.441= | NM_001353761.2:c.441G>A |
| CELF4 transcript variant 66 | NM_001353761.1:c.441= | NM_001353761.1:c.441G>A |
| CELF4 transcript variant 69 | NM_001353757.2:c.414= | NM_001353757.2:c.414G>A |
| CELF4 transcript variant 69 | NM_001353757.1:c.414= | NM_001353757.1:c.414G>A |
| CELF4 transcript variant 68 | NM_001353760.2:c.414= | NM_001353760.2:c.414G>A |
| CELF4 transcript variant 68 | NM_001353760.1:c.414= | NM_001353760.1:c.414G>A |
| CELF4 transcript variant 67 | NM_001353759.2:c.411= | NM_001353759.2:c.411G>A |
| CELF4 transcript variant 67 | NM_001353759.1:c.411= | NM_001353759.1:c.411G>A |
| CELF4 transcript variant 70 | NM_001353758.2:c.411= | NM_001353758.2:c.411G>A |
| CELF4 transcript variant 70 | NM_001353758.1:c.411= | NM_001353758.1:c.411G>A |
| CELF4 transcript variant X1 | XM_047437628.1:c.813= | XM_047437628.1:c.813G>A |
| CELF4 transcript variant X2 | XM_047437629.1:c.810= | XM_047437629.1:c.810G>A |
| CELF4 transcript variant X5 | XM_047437632.1:c.813= | XM_047437632.1:c.813G>A |
| CELF4 transcript variant X6 | XM_047437633.1:c.813= | XM_047437633.1:c.813G>A |
| CELF4 transcript variant X8 | XM_047437635.1:c.813= | XM_047437635.1:c.813G>A |
| CELF4 transcript variant X7 | XM_047437634.1:c.810= | XM_047437634.1:c.810G>A |
| CELF4 transcript variant X3 | XM_047437630.1:c.783= | XM_047437630.1:c.783G>A |
| CELF4 transcript variant X4 | XM_047437631.1:c.783= | XM_047437631.1:c.783G>A |
| CELF4 transcript variant X9 | XM_047437636.1:c.783= | XM_047437636.1:c.783G>A |
| CELF4 transcript variant X10 | XM_047437637.1:c.780= | XM_047437637.1:c.780G>A |
| CELF4 transcript variant X42 | XM_047437669.1:c.780= | XM_047437669.1:c.780G>A |
| CELF4 transcript variant X11 | XM_047437638.1:c.783= | XM_047437638.1:c.783G>A |
| CELF4 transcript variant X44 | XM_047437671.1:c.780= | XM_047437671.1:c.780G>A |
| CELF4 transcript variant X12 | XM_047437639.1:c.813= | XM_047437639.1:c.813G>A |
| CELF4 transcript variant X15 | XM_047437642.1:c.813= | XM_047437642.1:c.813G>A |
| CELF4 transcript variant X14 | XM_047437641.1:c.813= | XM_047437641.1:c.813G>A |
| CELF4 transcript variant X13 | XM_047437640.1:c.810= | XM_047437640.1:c.810G>A |
| CELF4 transcript variant X18 | XM_047437645.1:c.813= | XM_047437645.1:c.813G>A |
| CELF4 transcript variant X17 | XM_047437644.1:c.810= | XM_047437644.1:c.810G>A |
| CELF4 transcript variant X16 | XM_047437643.1:c.810= | XM_047437643.1:c.810G>A |
| CELF4 transcript variant X19 | XM_047437646.1:c.810= | XM_047437646.1:c.810G>A |
| CELF4 transcript variant X26 | XM_047437653.1:c.783= | XM_047437653.1:c.783G>A |
| CELF4 transcript variant X43 | XM_047437670.1:c.783= | XM_047437670.1:c.783G>A |
| CELF4 transcript variant X21 | XM_047437648.1:c.783= | XM_047437648.1:c.783G>A |
| CELF4 transcript variant X20 | XM_047437647.1:c.780= | XM_047437647.1:c.780G>A |
| CELF4 transcript variant X24 | XM_047437651.1:c.783= | XM_047437651.1:c.783G>A |
| CELF4 transcript variant X23 | XM_047437650.1:c.780= | XM_047437650.1:c.780G>A |
| CELF4 transcript variant X22 | XM_047437649.1:c.780= | XM_047437649.1:c.780G>A |
| CELF4 transcript variant X25 | XM_047437652.1:c.780= | XM_047437652.1:c.780G>A |
| CELF4 transcript variant X27 | XM_047437654.1:c.813= | XM_047437654.1:c.813G>A |
| CELF4 transcript variant X30 | XM_047437657.1:c.813= | XM_047437657.1:c.813G>A |
| CELF4 transcript variant X29 | XM_047437656.1:c.813= | XM_047437656.1:c.813G>A |
| CELF4 transcript variant X28 | XM_047437655.1:c.810= | XM_047437655.1:c.810G>A |
| CELF4 transcript variant X33 | XM_047437660.1:c.813= | XM_047437660.1:c.813G>A |
| CELF4 transcript variant X32 | XM_047437659.1:c.810= | XM_047437659.1:c.810G>A |
| CELF4 transcript variant X31 | XM_047437658.1:c.810= | XM_047437658.1:c.810G>A |
| CELF4 transcript variant X34 | XM_047437661.1:c.810= | XM_047437661.1:c.810G>A |
| CELF4 transcript variant X35 | XM_047437662.1:c.783= | XM_047437662.1:c.783G>A |
| CELF4 transcript variant X38 | XM_047437665.1:c.783= | XM_047437665.1:c.783G>A |
| CELF4 transcript variant X37 | XM_047437664.1:c.783= | XM_047437664.1:c.783G>A |
| CELF4 transcript variant X36 | XM_047437663.1:c.780= | XM_047437663.1:c.780G>A |
| CELF4 transcript variant X41 | XM_047437668.1:c.783= | XM_047437668.1:c.783G>A |
| CELF4 transcript variant X40 | XM_047437667.1:c.780= | XM_047437667.1:c.780G>A |
| CELF4 transcript variant X39 | XM_047437666.1:c.780= | XM_047437666.1:c.780G>A |
| CUGBP Elav-like family member 4 isoform 1 | NP_064565.1:p.Gln271= | NP_064565.1:p.Gln271= |
| CUGBP Elav-like family member 4 isoform 6 | NP_001340669.1:p.Gln271= | NP_001340669.1:p.Gln271= |
| CUGBP Elav-like family member 4 isoform 7 | NP_001340678.1:p.Gln270= | NP_001340678.1:p.Gln270= |
| CUGBP Elav-like family member 4 isoform 11 | NP_001340664.1:p.Gln260= | NP_001340664.1:p.Gln260= |
| CUGBP Elav-like family member 4 isoform 12 | NP_001340662.1:p.Gln259= | NP_001340662.1:p.Gln259= |
| CUGBP Elav-like family member 4 isoform 8 | NP_001340663.1:p.Gln271= | NP_001340663.1:p.Gln271= |
| CUGBP Elav-like family member 4 isoform 10 | NP_001340675.1:p.Gln270= | NP_001340675.1:p.Gln270= |
| CUGBP Elav-like family member 4 isoform 9 | NP_001340660.1:p.Gln271= | NP_001340660.1:p.Gln271= |
| CUGBP Elav-like family member 4 isoform 18 | NP_001340671.1:p.Gln270= | NP_001340671.1:p.Gln270= |
| CUGBP Elav-like family member 4 isoform 13 | NP_001340632.1:p.Gln261= | NP_001340632.1:p.Gln261= |
| CUGBP Elav-like family member 4 isoform 15 | NP_001340670.1:p.Gln260= | NP_001340670.1:p.Gln260= |
| CUGBP Elav-like family member 4 isoform 14 | NP_001340655.1:p.Gln260= | NP_001340655.1:p.Gln260= |
| CUGBP Elav-like family member 4 isoform 16 | NP_001340657.1:p.Gln260= | NP_001340657.1:p.Gln260= |
| CUGBP Elav-like family member 4 isoform 17 | NP_001340668.1:p.Gln259= | NP_001340668.1:p.Gln259= |
| CUGBP Elav-like family member 4 isoform 20 | NP_001340646.1:p.Gln261= | NP_001340646.1:p.Gln261= |
| CUGBP Elav-like family member 4 isoform 21 | NP_001340636.1:p.Gln260= | NP_001340636.1:p.Gln260= |
| CUGBP Elav-like family member 4 isoform 22 | NP_001340634.1:p.Gln259= | NP_001340634.1:p.Gln259= |
| CUGBP Elav-like family member 4 isoform 25 | NP_001340680.1:p.Gln271= | NP_001340680.1:p.Gln271= |
| CUGBP Elav-like family member 4 isoform 24 | NP_001340673.1:p.Gln271= | NP_001340673.1:p.Gln271= |
| CUGBP Elav-like family member 4 isoform 23 | NP_001340627.1:p.Gln270= | NP_001340627.1:p.Gln270= |
| CUGBP Elav-like family member 4 isoform 2 | NP_001020258.1:p.Gln270= | NP_001020258.1:p.Gln270= |
| CUGBP Elav-like family member 4 isoform 28 | NP_001340674.1:p.Gln270= | NP_001340674.1:p.Gln270= |
| CUGBP Elav-like family member 4 isoform 27 | NP_001340667.1:p.Gln270= | NP_001340667.1:p.Gln270= |
| CUGBP Elav-like family member 4 isoform 26 | NP_001340653.1:p.Gln271= | NP_001340653.1:p.Gln271= |
| CUGBP Elav-like family member 4 isoform 5 | NP_001317532.1:p.Gln270= | NP_001317532.1:p.Gln270= |
| CUGBP Elav-like family member 4 isoform 3 | NP_001020259.1:p.Gln269= | NP_001020259.1:p.Gln269= |
| CUGBP Elav-like family member 4 isoform 30 | NP_001340647.1:p.Gln270= | NP_001340647.1:p.Gln270= |
| CUGBP Elav-like family member 4 isoform 29 | NP_001340631.1:p.Gln269= | NP_001340631.1:p.Gln269= |
| CUGBP Elav-like family member 4 isoform 31 | NP_001340641.1:p.Gln269= | NP_001340641.1:p.Gln269= |
| CUGBP Elav-like family member 4 isoform 34 | NP_001340681.1:p.Gln260= | NP_001340681.1:p.Gln260= |
| CUGBP Elav-like family member 4 isoform 33 | NP_001340677.1:p.Gln261= | NP_001340677.1:p.Gln261= |
| CUGBP Elav-like family member 4 isoform 32 | NP_001340638.1:p.Gln260= | NP_001340638.1:p.Gln260= |
| CUGBP Elav-like family member 4 isoform 19 | NP_001340644.1:p.Gln261= | NP_001340644.1:p.Gln261= |
| CUGBP Elav-like family member 4 isoform 40 | NP_001340684.1:p.Gln259= | NP_001340684.1:p.Gln259= |
| CUGBP Elav-like family member 4 isoform 39 | NP_001340682.1:p.Gln260= | NP_001340682.1:p.Gln260= |
| CUGBP Elav-like family member 4 isoform 38 | NP_001340679.1:p.Gln260= | NP_001340679.1:p.Gln260= |
| CUGBP Elav-like family member 4 isoform 37 | NP_001340650.1:p.Gln260= | NP_001340650.1:p.Gln260= |
| CUGBP Elav-like family member 4 isoform 36 | NP_001340639.1:p.Gln261= | NP_001340639.1:p.Gln261= |
| CUGBP Elav-like family member 4 isoform 35 | NP_001340624.1:p.Gln260= | NP_001340624.1:p.Gln260= |
| CUGBP Elav-like family member 4 isoform 43 | NP_001340654.1:p.Gln259= | NP_001340654.1:p.Gln259= |
| CUGBP Elav-like family member 4 isoform 42 | NP_001340643.1:p.Gln260= | NP_001340643.1:p.Gln260= |
| CUGBP Elav-like family member 4 isoform 41 | NP_001340640.1:p.Gln259= | NP_001340640.1:p.Gln259= |
| CUGBP Elav-like family member 4 isoform 44 | NP_001340637.1:p.Gln271= | NP_001340637.1:p.Gln271= |
| CUGBP Elav-like family member 4 isoform 47 | NP_001340672.1:p.Gln271= | NP_001340672.1:p.Gln271= |
| CUGBP Elav-like family member 4 isoform 46 | NP_001340652.1:p.Gln270= | NP_001340652.1:p.Gln270= |
| CUGBP Elav-like family member 4 isoform 45 | NP_001340625.1:p.Gln270= | NP_001340625.1:p.Gln270= |
| CUGBP Elav-like family member 4 isoform 52 | NP_001340683.1:p.Gln269= | NP_001340683.1:p.Gln269= |
| CUGBP Elav-like family member 4 isoform 51 | NP_001340676.1:p.Gln270= | NP_001340676.1:p.Gln270= |
| CUGBP Elav-like family member 4 isoform 50 | NP_001340665.1:p.Gln271= | NP_001340665.1:p.Gln271= |
| CUGBP Elav-like family member 4 isoform 49 | NP_001340659.1:p.Gln270= | NP_001340659.1:p.Gln270= |
| CUGBP Elav-like family member 4 isoform 48 | NP_001340658.1:p.Gln270= | NP_001340658.1:p.Gln270= |
| CUGBP Elav-like family member 4 isoform 54 | NP_001340666.1:p.Gln270= | NP_001340666.1:p.Gln270= |
| CUGBP Elav-like family member 4 isoform 53 | NP_001340645.1:p.Gln269= | NP_001340645.1:p.Gln269= |
| CUGBP Elav-like family member 4 isoform 4 | NP_001020260.1:p.Gln261= | NP_001020260.1:p.Gln261= |
| CUGBP Elav-like family member 4 isoform 58 | NP_001340648.1:p.Gln261= | NP_001340648.1:p.Gln261= |
| CUGBP Elav-like family member 4 isoform 57 | NP_001340642.1:p.Gln260= | NP_001340642.1:p.Gln260= |
| CUGBP Elav-like family member 4 isoform 56 | NP_001340629.1:p.Gln261= | NP_001340629.1:p.Gln261= |
| CUGBP Elav-like family member 4 isoform 55 | NP_001340626.1:p.Gln260= | NP_001340626.1:p.Gln260= |
| CUGBP Elav-like family member 4 isoform 63 | NP_001340661.1:p.Gln260= | NP_001340661.1:p.Gln260= |
| CUGBP Elav-like family member 4 isoform 62 | NP_001340656.1:p.Gln260= | NP_001340656.1:p.Gln260= |
| CUGBP Elav-like family member 4 isoform 61 | NP_001340649.1:p.Gln261= | NP_001340649.1:p.Gln261= |
| CUGBP Elav-like family member 4 isoform 60 | NP_001340635.1:p.Gln259= | NP_001340635.1:p.Gln259= |
| CUGBP Elav-like family member 4 isoform 59 | NP_001340628.1:p.Gln260= | NP_001340628.1:p.Gln260= |
| CUGBP Elav-like family member 4 isoform 64 | NP_001340651.1:p.Gln259= | NP_001340651.1:p.Gln259= |
| CUGBP Elav-like family member 4 isoform 65 | NP_001340685.1:p.Gln147= | NP_001340685.1:p.Gln147= |
| CUGBP Elav-like family member 4 isoform 66 | NP_001340690.1:p.Gln147= | NP_001340690.1:p.Gln147= |
| CUGBP Elav-like family member 4 isoform 69 | NP_001340686.1:p.Gln138= | NP_001340686.1:p.Gln138= |
| CUGBP Elav-like family member 4 isoform 68 | NP_001340689.1:p.Gln138= | NP_001340689.1:p.Gln138= |
| CUGBP Elav-like family member 4 isoform 67 | NP_001340688.1:p.Gln137= | NP_001340688.1:p.Gln137= |
| CUGBP Elav-like family member 4 isoform 70 | NP_001340687.1:p.Gln137= | NP_001340687.1:p.Gln137= |
| CUGBP Elav-like family member 4 isoform X1 | XP_047293584.1:p.Gln271= | XP_047293584.1:p.Gln271= |
| CUGBP Elav-like family member 4 isoform X2 | XP_047293585.1:p.Gln270= | XP_047293585.1:p.Gln270= |
| CUGBP Elav-like family member 4 isoform X5 | XP_047293588.1:p.Gln271= | XP_047293588.1:p.Gln271= |
| CUGBP Elav-like family member 4 isoform X6 | XP_047293589.1:p.Gln271= | XP_047293589.1:p.Gln271= |
| CUGBP Elav-like family member 4 isoform X8 | XP_047293591.1:p.Gln271= | XP_047293591.1:p.Gln271= |
| CUGBP Elav-like family member 4 isoform X7 | XP_047293590.1:p.Gln270= | XP_047293590.1:p.Gln270= |
| CUGBP Elav-like family member 4 isoform X3 | XP_047293586.1:p.Gln261= | XP_047293586.1:p.Gln261= |
| CUGBP Elav-like family member 4 isoform X4 | XP_047293587.1:p.Gln261= | XP_047293587.1:p.Gln261= |
| CUGBP Elav-like family member 4 isoform X9 | XP_047293592.1:p.Gln261= | XP_047293592.1:p.Gln261= |
| CUGBP Elav-like family member 4 isoform X10 | XP_047293593.1:p.Gln260= | XP_047293593.1:p.Gln260= |
| CUGBP Elav-like family member 4 isoform X42 | XP_047293625.1:p.Gln260= | XP_047293625.1:p.Gln260= |
| CUGBP Elav-like family member 4 isoform X11 | XP_047293594.1:p.Gln261= | XP_047293594.1:p.Gln261= |
| CUGBP Elav-like family member 4 isoform X44 | XP_047293627.1:p.Gln260= | XP_047293627.1:p.Gln260= |
| CUGBP Elav-like family member 4 isoform X12 | XP_047293595.1:p.Gln271= | XP_047293595.1:p.Gln271= |
| CUGBP Elav-like family member 4 isoform X15 | XP_047293598.1:p.Gln271= | XP_047293598.1:p.Gln271= |
| CUGBP Elav-like family member 4 isoform X14 | XP_047293597.1:p.Gln271= | XP_047293597.1:p.Gln271= |
| CUGBP Elav-like family member 4 isoform X13 | XP_047293596.1:p.Gln270= | XP_047293596.1:p.Gln270= |
| CUGBP Elav-like family member 4 isoform X18 | XP_047293601.1:p.Gln271= | XP_047293601.1:p.Gln271= |
| CUGBP Elav-like family member 4 isoform X17 | XP_047293600.1:p.Gln270= | XP_047293600.1:p.Gln270= |
| CUGBP Elav-like family member 4 isoform X16 | XP_047293599.1:p.Gln270= | XP_047293599.1:p.Gln270= |
| CUGBP Elav-like family member 4 isoform X19 | XP_047293602.1:p.Gln270= | XP_047293602.1:p.Gln270= |
| CUGBP Elav-like family member 4 isoform X26 | XP_047293609.1:p.Gln261= | XP_047293609.1:p.Gln261= |
| CUGBP Elav-like family member 4 isoform X43 | XP_047293626.1:p.Gln261= | XP_047293626.1:p.Gln261= |
| CUGBP Elav-like family member 4 isoform X21 | XP_047293604.1:p.Gln261= | XP_047293604.1:p.Gln261= |
| CUGBP Elav-like family member 4 isoform X20 | XP_047293603.1:p.Gln260= | XP_047293603.1:p.Gln260= |
| CUGBP Elav-like family member 4 isoform X24 | XP_047293607.1:p.Gln261= | XP_047293607.1:p.Gln261= |
| CUGBP Elav-like family member 4 isoform X23 | XP_047293606.1:p.Gln260= | XP_047293606.1:p.Gln260= |
| CUGBP Elav-like family member 4 isoform X22 | XP_047293605.1:p.Gln260= | XP_047293605.1:p.Gln260= |
| CUGBP Elav-like family member 4 isoform X25 | XP_047293608.1:p.Gln260= | XP_047293608.1:p.Gln260= |
| CUGBP Elav-like family member 4 isoform X27 | XP_047293610.1:p.Gln271= | XP_047293610.1:p.Gln271= |
| CUGBP Elav-like family member 4 isoform X30 | XP_047293613.1:p.Gln271= | XP_047293613.1:p.Gln271= |
| CUGBP Elav-like family member 4 isoform X29 | XP_047293612.1:p.Gln271= | XP_047293612.1:p.Gln271= |
| CUGBP Elav-like family member 4 isoform X28 | XP_047293611.1:p.Gln270= | XP_047293611.1:p.Gln270= |
| CUGBP Elav-like family member 4 isoform X33 | XP_047293616.1:p.Gln271= | XP_047293616.1:p.Gln271= |
| CUGBP Elav-like family member 4 isoform X32 | XP_047293615.1:p.Gln270= | XP_047293615.1:p.Gln270= |
| CUGBP Elav-like family member 4 isoform X31 | XP_047293614.1:p.Gln270= | XP_047293614.1:p.Gln270= |
| CUGBP Elav-like family member 4 isoform X34 | XP_047293617.1:p.Gln270= | XP_047293617.1:p.Gln270= |
| CUGBP Elav-like family member 4 isoform X35 | XP_047293618.1:p.Gln261= | XP_047293618.1:p.Gln261= |
| CUGBP Elav-like family member 4 isoform X38 | XP_047293621.1:p.Gln261= | XP_047293621.1:p.Gln261= |
| CUGBP Elav-like family member 4 isoform X37 | XP_047293620.1:p.Gln261= | XP_047293620.1:p.Gln261= |
| CUGBP Elav-like family member 4 isoform X36 | XP_047293619.1:p.Gln260= | XP_047293619.1:p.Gln260= |
| CUGBP Elav-like family member 4 isoform X41 | XP_047293624.1:p.Gln261= | XP_047293624.1:p.Gln261= |
| CUGBP Elav-like family member 4 isoform X40 | XP_047293623.1:p.Gln260= | XP_047293623.1:p.Gln260= |
| CUGBP Elav-like family member 4 isoform X39 | XP_047293622.1:p.Gln260= | XP_047293622.1:p.Gln260= |
Help
Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.
1 SubSNP,
1 Frequency
submissions
| No | Submitter | Submission ID | Date (Build) |
|---|---|---|---|
| 1 | GNOMAD | ss2743269597 | Nov 08, 2017 (151) |
| 2 | gnomAD - Exomes | NC_000018.9 - 34853115 | Jul 13, 2019 (153) |
Help
History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).
Help
Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.
No publications for rs1472894593
Help
The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.
Genome context:
Select flank length:
Genomic regions, transcripts, and products
Top▲
Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.