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Chromosome 15 - NC_000015.10
Genomic Sequence: NC_000015.10 Chromosome 15 Reference GRCh38.p14 Primary Assembly NW_011332701.1 Chromosome 15 Reference GRCh38.p14 PATCHES NW_012132920.1 Chromosome 15 Reference GRCh38.p14 PATCHES NT_187660.1 Chromosome 15 Reference GRCh38.p14 ALT_REF_LOCI_2 NG_042863.1 RefSeqGene NC_060939.1 Chromosome 15 Alternate T2T-CHM13v2.0 NC_000015.9 Chromosome 15 Reference GRCh37.p13 Primary Assembly
Go to nucleotide: Graphics FASTA GenBank
See all (32) citations in PubMed
Find tests for this gene in the NIH Genetic Testing Registry (GTR)
Review eQTL and phenotype association data in this region using PheGenI
See variants in ClinVar
See studies and variants in dbVar
See Variation Viewer (GRCh37.p13)
See Variation Viewer (GRCh38)
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These reference sequences exist independently of genome builds. Explain
These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.
NG_042863.1 RefSeqGene
NM_001103184.4 → NP_001096654.1 formin-1 isoform b
See identical proteins and their annotated locations for NP_001096654.1
Status: REVIEWED
NM_001277313.2 → NP_001264242.1 formin-1 isoform a
See identical proteins and their annotated locations for NP_001264242.1
NM_001277314.2 → NP_001264243.1 formin-1 isoform c
The following sections contain reference sequences that belong to a specific genome build. Explain
This section includes genomic Reference Sequences (RefSeqs) from all assemblies on which this gene is annotated, such as RefSeqs for chromosomes and scaffolds (contigs) from both reference and alternate assemblies. Model RNAs and proteins are also reported here.
NC_000015.10 Reference GRCh38.p14 Primary Assembly
XM_011521509.4 → XP_011519811.1 formin-1 isoform X9
XM_011521504.4 → XP_011519806.1 formin-1 isoform X1
See identical proteins and their annotated locations for XP_011519806.1
XM_047432436.1 → XP_047288392.1 formin-1 isoform X4
XM_047432440.1 → XP_047288396.1 formin-1 isoform X12
XM_017022134.3 → XP_016877623.1 formin-1 isoform X13
XM_017022132.3 → XP_016877621.1 formin-1 isoform X10
XM_011521511.4 → XP_011519813.1 formin-1 isoform X11
XM_047432441.1 → XP_047288397.1 formin-1 isoform X14
XM_047432437.1 → XP_047288393.1 formin-1 isoform X6
XM_011521505.3 → XP_011519807.1 formin-1 isoform X2
XM_047432438.1 → XP_047288394.1 formin-1 isoform X7
XM_017022131.2 → XP_016877620.1 formin-1 isoform X3
XM_047432439.1 → XP_047288395.1 formin-1 isoform X8
XM_011521507.3 → XP_011519809.1 formin-1 isoform X5
NW_011332701.1 Reference GRCh38.p14 PATCHES
NW_012132920.1 Reference GRCh38.p14 PATCHES
NT_187660.1 Reference GRCh38.p14 ALT_REF_LOCI_2
NC_060939.1 Alternate T2T-CHM13v2.0
XM_054377823.1 → XP_054233798.1 formin-1 isoform X9
XM_054377815.1 → XP_054233790.1 formin-1 isoform X1
XM_054377818.1 → XP_054233793.1 formin-1 isoform X4
XM_054377827.1 → XP_054233802.1 formin-1 isoform X12
XM_054377828.1 → XP_054233803.1 formin-1 isoform X13
XM_054377824.1 → XP_054233799.1 formin-1 isoform X10
XM_054377826.1 → XP_054233801.1 formin-1 isoform X11
XM_054377825.1 → XP_054233800.1 formin-1 isoform X15
XM_054377820.1 → XP_054233795.1 formin-1 isoform X6
XM_054377816.1 → XP_054233791.1 formin-1 isoform X2
XM_054377821.1 → XP_054233796.1 formin-1 isoform X7
XM_054377817.1 → XP_054233792.1 formin-1 isoform X3
XM_054377822.1 → XP_054233797.1 formin-1 isoform X8
XM_054377819.1 → XP_054233794.1 formin-1 isoform X5
The following Reference Sequences have been suppressed. Explain
These RefSeqs were suppressed for the cited reason(s). Suppressed RefSeqs do not appear in BLAST databases, related sequence links, or BLAST links (BLink), but may still be retrieved by clicking on their accession.version below.
NM_198500.1: Suppressed sequence
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