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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.
Genomic
-
NG_009269.1 RefSeqGene
- Range
-
4998..115797
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
mRNA and Protein(s)
-
NM_001042424.3 → NP_001035889.1 histone-lysine N-methyltransferase NSD2 isoform 1
See identical proteins and their annotated locations for NP_001035889.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (10) contains a novel 5' non-coding exon compared to transcript variant 1, hence has a different 5' UTR. However, it encodes the same isoform (1) as transcript variants 1, 2 and 3.
- Source sequence(s)
-
AC105448, AF071593, BC032731, BC094825, BM982021, CX866583
- Consensus CDS
-
CCDS33940.1
- UniProtKB/Swiss-Prot
- A2A2T2, A2A2T3, A2A2T4, A7MCZ1, D3DVQ2, O96028, O96031, Q4VBY8, Q672J1, Q6IS00, Q86V01, Q9BZB4, Q9UI92, Q9UPR2
- Related
- ENSP00000423972.1, ENST00000508803.6
- Conserved Domains (11) summary
-
- cd05837
Location:218 → 337
- MSH6_like; The PWWP domain is present in MSH6, a mismatch repair protein homologous to bacterial MutS. The PWWP domain of histone-lysine N-methyltransferase, also known as Nuclear SET domain-containing protein 3, is also included. Mutations in MSH6 have been ...
- cd05838
Location:878 → 972
- WHSC1_related; The PWWP domain was first identified in the WHSC1 (Wolf-Hirschhorn syndrome candidate 1) protein, a protein implicated in Wolf-Hirschhorn syndrome (WHS). When translocated, WHSC1 plays a role in lymphoid multiple myeloma (MM) disease, also known as ...
- smart00570
Location:1012 → 1062
- AWS; associated with SET domains
- smart00317
Location:1063 → 1186
- SET; SET (Su(var)3-9, Enhancer-of-zeste, Trithorax) domain
- COG5034
Location:546 → 710
- TNG2; Chromatin remodeling protein, contains PhD zinc finger [Chromatin structure and dynamics]
- cd00084
Location:458 → 507
- HMG-box; High Mobility Group (HMG)-box is found in a variety of eukaryotic chromosomal proteins and transcription factors. HMGs bind to the minor groove of DNA and have been classified by DNA binding preferences. Two phylogenically distinct groups of Class I ...
- cd15648
Location:669 → 711
- PHD1_NSD1_2; PHD finger 1 found in nuclear receptor-binding SET domain-containing protein NSD1 and NSD2
- cd15651
Location:716 → 762
- PHD2_NSD2; PHD finger 2 found in nuclear SET domain-containing protein 2 (NSD2)
- cd15654
Location:763 → 816
- PHD3_NSD2; PHD finger 3 found in nuclear SET domain-containing protein 2 (NSD2)
- cd15657
Location:833 → 873
- PHD4_NSD2; PHD finger 4 found in nuclear SET domain-containing protein 2 (NSD2)
- cd15660
Location:1241 → 1283
- PHD5_NSD2; PHD finger 5 found in nuclear SET domain-containing protein 2 (NSD2)
-
NM_007331.2 → NP_015627.1 histone-lysine N-methyltransferase NSD2 isoform 4
See identical proteins and their annotated locations for NP_015627.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (8) contains an additional fragment beyond the 3' end of exon 11, and lacks exons 12-25, as compared to variant 1. This fragment shifts the reading frame and introduces an immediate translation termination. This variant encodes isoform 4, which is much shorter and has a different C-terminus from isoform 1.
- Source sequence(s)
-
AF083391
- Consensus CDS
-
CCDS46999.1
- UniProtKB/TrEMBL
-
A0A7P0P278
- Related
- ENSP00000399251.2, ENST00000420906.6
- Conserved Domains (2) summary
-
- cd05837
Location:218 → 337
- MSH6_like; The PWWP domain is present in MSH6, a mismatch repair protein homologous to bacterial MutS. The PWWP domain of histone-lysine N-methyltransferase, also known as Nuclear SET domain-containing protein 3, is also included. Mutations in MSH6 have been ...
- cd00084
Location:458 → 507
- HMG-box; High Mobility Group (HMG)-box is found in a variety of eukaryotic chromosomal proteins and transcription factors. HMGs bind to the minor groove of DNA and have been classified by DNA binding preferences. Two phylogenically distinct groups of Class I ...
-
NM_133330.3 → NP_579877.1 histone-lysine N-methyltransferase NSD2 isoform 1
See identical proteins and their annotated locations for NP_579877.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (1) lacks exon 12, and contains only 24 exons. It encodes the longest isoform (1).
- Source sequence(s)
-
AF083386, AI695058
- Consensus CDS
-
CCDS33940.1
- UniProtKB/Swiss-Prot
- A2A2T2, A2A2T3, A2A2T4, A7MCZ1, D3DVQ2, O96028, O96031, Q4VBY8, Q672J1, Q6IS00, Q86V01, Q9BZB4, Q9UI92, Q9UPR2
- Related
- ENSP00000372351.3, ENST00000382895.7
- Conserved Domains (11) summary
-
- cd05837
Location:218 → 337
- MSH6_like; The PWWP domain is present in MSH6, a mismatch repair protein homologous to bacterial MutS. The PWWP domain of histone-lysine N-methyltransferase, also known as Nuclear SET domain-containing protein 3, is also included. Mutations in MSH6 have been ...
- cd05838
Location:878 → 972
- WHSC1_related; The PWWP domain was first identified in the WHSC1 (Wolf-Hirschhorn syndrome candidate 1) protein, a protein implicated in Wolf-Hirschhorn syndrome (WHS). When translocated, WHSC1 plays a role in lymphoid multiple myeloma (MM) disease, also known as ...
- smart00570
Location:1012 → 1062
- AWS; associated with SET domains
- smart00317
Location:1063 → 1186
- SET; SET (Su(var)3-9, Enhancer-of-zeste, Trithorax) domain
- COG5034
Location:546 → 710
- TNG2; Chromatin remodeling protein, contains PhD zinc finger [Chromatin structure and dynamics]
- cd00084
Location:458 → 507
- HMG-box; High Mobility Group (HMG)-box is found in a variety of eukaryotic chromosomal proteins and transcription factors. HMGs bind to the minor groove of DNA and have been classified by DNA binding preferences. Two phylogenically distinct groups of Class I ...
- cd15648
Location:669 → 711
- PHD1_NSD1_2; PHD finger 1 found in nuclear receptor-binding SET domain-containing protein NSD1 and NSD2
- cd15651
Location:716 → 762
- PHD2_NSD2; PHD finger 2 found in nuclear SET domain-containing protein 2 (NSD2)
- cd15654
Location:763 → 816
- PHD3_NSD2; PHD finger 3 found in nuclear SET domain-containing protein 2 (NSD2)
- cd15657
Location:833 → 873
- PHD4_NSD2; PHD finger 4 found in nuclear SET domain-containing protein 2 (NSD2)
- cd15660
Location:1241 → 1283
- PHD5_NSD2; PHD finger 5 found in nuclear SET domain-containing protein 2 (NSD2)
-
NM_133331.3 → NP_579878.1 histone-lysine N-methyltransferase NSD2 isoform 1
See identical proteins and their annotated locations for NP_579878.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (2) lacks exon 2 in the 5' UTR, as compared to variant 1. It encodes the same isoform (1) as variants 1 and 3.
- Source sequence(s)
-
AF083387, AI695058
- Consensus CDS
-
CCDS33940.1
- UniProtKB/Swiss-Prot
- A2A2T2, A2A2T3, A2A2T4, A7MCZ1, D3DVQ2, O96028, O96031, Q4VBY8, Q672J1, Q6IS00, Q86V01, Q9BZB4, Q9UI92, Q9UPR2
- Related
- ENSP00000372348.2, ENST00000382892.6
- Conserved Domains (11) summary
-
- cd05837
Location:218 → 337
- MSH6_like; The PWWP domain is present in MSH6, a mismatch repair protein homologous to bacterial MutS. The PWWP domain of histone-lysine N-methyltransferase, also known as Nuclear SET domain-containing protein 3, is also included. Mutations in MSH6 have been ...
- cd05838
Location:878 → 972
- WHSC1_related; The PWWP domain was first identified in the WHSC1 (Wolf-Hirschhorn syndrome candidate 1) protein, a protein implicated in Wolf-Hirschhorn syndrome (WHS). When translocated, WHSC1 plays a role in lymphoid multiple myeloma (MM) disease, also known as ...
- smart00570
Location:1012 → 1062
- AWS; associated with SET domains
- smart00317
Location:1063 → 1186
- SET; SET (Su(var)3-9, Enhancer-of-zeste, Trithorax) domain
- COG5034
Location:546 → 710
- TNG2; Chromatin remodeling protein, contains PhD zinc finger [Chromatin structure and dynamics]
- cd00084
Location:458 → 507
- HMG-box; High Mobility Group (HMG)-box is found in a variety of eukaryotic chromosomal proteins and transcription factors. HMGs bind to the minor groove of DNA and have been classified by DNA binding preferences. Two phylogenically distinct groups of Class I ...
- cd15648
Location:669 → 711
- PHD1_NSD1_2; PHD finger 1 found in nuclear receptor-binding SET domain-containing protein NSD1 and NSD2
- cd15651
Location:716 → 762
- PHD2_NSD2; PHD finger 2 found in nuclear SET domain-containing protein 2 (NSD2)
- cd15654
Location:763 → 816
- PHD3_NSD2; PHD finger 3 found in nuclear SET domain-containing protein 2 (NSD2)
- cd15657
Location:833 → 873
- PHD4_NSD2; PHD finger 4 found in nuclear SET domain-containing protein 2 (NSD2)
- cd15660
Location:1241 → 1283
- PHD5_NSD2; PHD finger 5 found in nuclear SET domain-containing protein 2 (NSD2)
-
NM_133334.2 → NP_579889.1 histone-lysine N-methyltransferase NSD2 isoform 3
See identical proteins and their annotated locations for NP_579889.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (7) is missing most of the exons from the 3' end compared to variant 1. It has a different 3' UTR and encodes a shorter isoform (3) with a different C-terminus compared to isoform 1.
- Source sequence(s)
-
AF071594, AL132868
- Consensus CDS
-
CCDS3356.1
- UniProtKB/TrEMBL
-
A0A7P0P278
- Related
- ENSP00000381311.1, ENST00000398261.6
- Conserved Domains (2) summary
-
- cd05837
Location:218 → 337
- MSH6_like; The PWWP domain is present in MSH6, a mismatch repair protein homologous to bacterial MutS. The PWWP domain of histone-lysine N-methyltransferase, also known as Nuclear SET domain-containing protein 3, is also included. Mutations in MSH6 have been ...
- cd00084
Location:458 → 507
- HMG-box; High Mobility Group (HMG)-box is found in a variety of eukaryotic chromosomal proteins and transcription factors. HMGs bind to the minor groove of DNA and have been classified by DNA binding preferences. Two phylogenically distinct groups of Class I ...
-
NM_133335.4 → NP_579890.1 histone-lysine N-methyltransferase NSD2 isoform 1
See identical proteins and their annotated locations for NP_579890.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (3) lacks exons 2 and 3 in the 5' UTR, as compared to variant 1. It encodes the same isoform (1) as variants 1 and 2.
- Source sequence(s)
-
AF071593, AF083388, AI339675, AI695058
- Consensus CDS
-
CCDS33940.1
- UniProtKB/Swiss-Prot
- A2A2T2, A2A2T3, A2A2T4, A7MCZ1, D3DVQ2, O96028, O96031, Q4VBY8, Q672J1, Q6IS00, Q86V01, Q9BZB4, Q9UI92, Q9UPR2
- Related
- ENSP00000372347.5, ENST00000382891.9
- Conserved Domains (11) summary
-
- cd05837
Location:218 → 337
- MSH6_like; The PWWP domain is present in MSH6, a mismatch repair protein homologous to bacterial MutS. The PWWP domain of histone-lysine N-methyltransferase, also known as Nuclear SET domain-containing protein 3, is also included. Mutations in MSH6 have been ...
- cd05838
Location:878 → 972
- WHSC1_related; The PWWP domain was first identified in the WHSC1 (Wolf-Hirschhorn syndrome candidate 1) protein, a protein implicated in Wolf-Hirschhorn syndrome (WHS). When translocated, WHSC1 plays a role in lymphoid multiple myeloma (MM) disease, also known as ...
- smart00570
Location:1012 → 1062
- AWS; associated with SET domains
- smart00317
Location:1063 → 1186
- SET; SET (Su(var)3-9, Enhancer-of-zeste, Trithorax) domain
- COG5034
Location:546 → 710
- TNG2; Chromatin remodeling protein, contains PhD zinc finger [Chromatin structure and dynamics]
- cd00084
Location:458 → 507
- HMG-box; High Mobility Group (HMG)-box is found in a variety of eukaryotic chromosomal proteins and transcription factors. HMGs bind to the minor groove of DNA and have been classified by DNA binding preferences. Two phylogenically distinct groups of Class I ...
- cd15648
Location:669 → 711
- PHD1_NSD1_2; PHD finger 1 found in nuclear receptor-binding SET domain-containing protein NSD1 and NSD2
- cd15651
Location:716 → 762
- PHD2_NSD2; PHD finger 2 found in nuclear SET domain-containing protein 2 (NSD2)
- cd15654
Location:763 → 816
- PHD3_NSD2; PHD finger 3 found in nuclear SET domain-containing protein 2 (NSD2)
- cd15657
Location:833 → 873
- PHD4_NSD2; PHD finger 4 found in nuclear SET domain-containing protein 2 (NSD2)
- cd15660
Location:1241 → 1283
- PHD5_NSD2; PHD finger 5 found in nuclear SET domain-containing protein 2 (NSD2)
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.
Reference GRCh38.p14 Primary Assembly
Genomic
-
NC_000004.12 Reference GRCh38.p14 Primary Assembly
- Range
-
1871393..1982192
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
mRNA and Protein(s)
-
XM_047416138.1 → XP_047272094.1 histone-lysine N-methyltransferase NSD2 isoform X1
- UniProtKB/Swiss-Prot
- A2A2T2, A2A2T3, A2A2T4, A7MCZ1, D3DVQ2, O96028, O96031, Q4VBY8, Q672J1, Q6IS00, Q86V01, Q9BZB4, Q9UI92, Q9UPR2
-
XM_047416141.1 → XP_047272097.1 histone-lysine N-methyltransferase NSD2 isoform X2
-
XM_047416137.1 → XP_047272093.1 histone-lysine N-methyltransferase NSD2 isoform X1
- UniProtKB/Swiss-Prot
- A2A2T2, A2A2T3, A2A2T4, A7MCZ1, D3DVQ2, O96028, O96031, Q4VBY8, Q672J1, Q6IS00, Q86V01, Q9BZB4, Q9UI92, Q9UPR2
-
XM_005248002.4 → XP_005248059.1 histone-lysine N-methyltransferase NSD2 isoform X2
- Conserved Domains (10) summary
-
- cd05837
Location:218 → 337
- MSH6_like; The PWWP domain is present in MSH6, a mismatch repair protein homologous to bacterial MutS. The PWWP domain of histone-lysine N-methyltransferase, also known as Nuclear SET domain-containing protein 3, is also included. Mutations in MSH6 have been ...
- cd05838
Location:809 → 903
- WHSC1_related; The PWWP domain was first identified in the WHSC1 (Wolf-Hirschhorn syndrome candidate 1) protein, a protein implicated in Wolf-Hirschhorn syndrome (WHS). When translocated, WHSC1 plays a role in lymphoid multiple myeloma (MM) disease, also known as ...
- smart00570
Location:943 → 993
- AWS; associated with SET domains
- smart00317
Location:994 → 1117
- SET; SET (Su(var)3-9, Enhancer-of-zeste, Trithorax) domain
- cd00084
Location:458 → 507
- HMG-box; High Mobility Group (HMG)-box is found in a variety of eukaryotic chromosomal proteins and transcription factors. HMGs bind to the minor groove of DNA and have been classified by DNA binding preferences. Two phylogenically distinct groups of Class I ...
- cd15648
Location:600 → 642
- PHD1_NSD1_2; PHD finger 1 found in nuclear receptor-binding SET domain-containing protein NSD1 and NSD2
- cd15651
Location:647 → 693
- PHD2_NSD2; PHD finger 2 found in nuclear SET domain-containing protein 2 (NSD2)
- cd15654
Location:694 → 747
- PHD3_NSD2; PHD finger 3 found in nuclear SET domain-containing protein 2 (NSD2)
- cd15660
Location:1172 → 1214
- PHD5_NSD2; PHD finger 5 found in nuclear SET domain-containing protein 2 (NSD2)
- cl22851
Location:764 → 804
- PHD_SF; PHD finger superfamily
-
XM_047416143.1 → XP_047272099.1 histone-lysine N-methyltransferase NSD2 isoform X3
- UniProtKB/TrEMBL
-
A0A7P0P278
- Related
- ENSP00000427516.2, ENST00000512700.2
-
XM_047416144.1 → XP_047272100.1 histone-lysine N-methyltransferase NSD2 isoform X4
- UniProtKB/TrEMBL
-
A0A7P0P278
- Related
- ENSP00000308780.6, ENST00000312087.10
-
XM_005248005.4 → XP_005248062.1 histone-lysine N-methyltransferase NSD2 isoform X4
See identical proteins and their annotated locations for XP_005248062.1
- UniProtKB/TrEMBL
-
A0A7P0P278
- Conserved Domains (2) summary
-
- cd05837
Location:218 → 337
- MSH6_like; The PWWP domain is present in MSH6, a mismatch repair protein homologous to bacterial MutS. The PWWP domain of histone-lysine N-methyltransferase, also known as Nuclear SET domain-containing protein 3, is also included. Mutations in MSH6 have been ...
- cd00084
Location:458 → 507
- HMG-box; High Mobility Group (HMG)-box is found in a variety of eukaryotic chromosomal proteins and transcription factors. HMGs bind to the minor groove of DNA and have been classified by DNA binding preferences. Two phylogenically distinct groups of Class I ...
-
XM_047416142.1 → XP_047272098.1 histone-lysine N-methyltransferase NSD2 isoform X2
-
XM_005248001.5 → XP_005248058.1 histone-lysine N-methyltransferase NSD2 isoform X1
See identical proteins and their annotated locations for XP_005248058.1
- UniProtKB/Swiss-Prot
- A2A2T2, A2A2T3, A2A2T4, A7MCZ1, D3DVQ2, O96028, O96031, Q4VBY8, Q672J1, Q6IS00, Q86V01, Q9BZB4, Q9UI92, Q9UPR2
- Conserved Domains (11) summary
-
- cd05837
Location:218 → 337
- MSH6_like; The PWWP domain is present in MSH6, a mismatch repair protein homologous to bacterial MutS. The PWWP domain of histone-lysine N-methyltransferase, also known as Nuclear SET domain-containing protein 3, is also included. Mutations in MSH6 have been ...
- cd05838
Location:878 → 972
- WHSC1_related; The PWWP domain was first identified in the WHSC1 (Wolf-Hirschhorn syndrome candidate 1) protein, a protein implicated in Wolf-Hirschhorn syndrome (WHS). When translocated, WHSC1 plays a role in lymphoid multiple myeloma (MM) disease, also known as ...
- smart00570
Location:1012 → 1062
- AWS; associated with SET domains
- smart00317
Location:1063 → 1186
- SET; SET (Su(var)3-9, Enhancer-of-zeste, Trithorax) domain
- COG5034
Location:546 → 710
- TNG2; Chromatin remodeling protein, contains PhD zinc finger [Chromatin structure and dynamics]
- cd00084
Location:458 → 507
- HMG-box; High Mobility Group (HMG)-box is found in a variety of eukaryotic chromosomal proteins and transcription factors. HMGs bind to the minor groove of DNA and have been classified by DNA binding preferences. Two phylogenically distinct groups of Class I ...
- cd15648
Location:669 → 711
- PHD1_NSD1_2; PHD finger 1 found in nuclear receptor-binding SET domain-containing protein NSD1 and NSD2
- cd15651
Location:716 → 762
- PHD2_NSD2; PHD finger 2 found in nuclear SET domain-containing protein 2 (NSD2)
- cd15654
Location:763 → 816
- PHD3_NSD2; PHD finger 3 found in nuclear SET domain-containing protein 2 (NSD2)
- cd15657
Location:833 → 873
- PHD4_NSD2; PHD finger 4 found in nuclear SET domain-containing protein 2 (NSD2)
- cd15660
Location:1241 → 1283
- PHD5_NSD2; PHD finger 5 found in nuclear SET domain-containing protein 2 (NSD2)
-
XM_047416139.1 → XP_047272095.1 histone-lysine N-methyltransferase NSD2 isoform X1
- UniProtKB/Swiss-Prot
- A2A2T2, A2A2T3, A2A2T4, A7MCZ1, D3DVQ2, O96028, O96031, Q4VBY8, Q672J1, Q6IS00, Q86V01, Q9BZB4, Q9UI92, Q9UPR2
-
XM_011513560.3 → XP_011511862.1 histone-lysine N-methyltransferase NSD2 isoform X5
See identical proteins and their annotated locations for XP_011511862.1
- UniProtKB/Swiss-Prot
-
O96028
- Related
- ENSP00000372344.3, ENST00000382888.3
- Conserved Domains (4) summary
-
- cd05838
Location:97 → 191
- WHSC1_related; The PWWP domain was first identified in the WHSC1 (Wolf-Hirschhorn syndrome candidate 1) protein, a protein implicated in Wolf-Hirschhorn syndrome (WHS). When translocated, WHSC1 plays a role in lymphoid multiple myeloma (MM) disease, also known as ...
- smart00570
Location:231 → 281
- AWS; associated with SET domains
- smart00317
Location:282 → 405
- SET; SET (Su(var)3-9, Enhancer-of-zeste, Trithorax) domain
- cl22851
Location:460 → 502
- PHD_SF; PHD finger superfamily
Alternate T2T-CHM13v2.0
Genomic
-
NC_060928.1 Alternate T2T-CHM13v2.0
- Range
-
1869868..1980701
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
mRNA and Protein(s)
-
XM_054350799.1 → XP_054206774.1 histone-lysine N-methyltransferase NSD2 isoform X1
- UniProtKB/Swiss-Prot
- A2A2T2, A2A2T3, A2A2T4, A7MCZ1, D3DVQ2, O96028, O96031, Q4VBY8, Q672J1, Q6IS00, Q86V01, Q9BZB4, Q9UI92, Q9UPR2
-
XM_054350804.1 → XP_054206779.1 histone-lysine N-methyltransferase NSD2 isoform X2
-
XM_054350798.1 → XP_054206773.1 histone-lysine N-methyltransferase NSD2 isoform X1
- UniProtKB/Swiss-Prot
- A2A2T2, A2A2T3, A2A2T4, A7MCZ1, D3DVQ2, O96028, O96031, Q4VBY8, Q672J1, Q6IS00, Q86V01, Q9BZB4, Q9UI92, Q9UPR2
-
XM_054350802.1 → XP_054206777.1 histone-lysine N-methyltransferase NSD2 isoform X2
-
XM_054350803.1 → XP_054206778.1 histone-lysine N-methyltransferase NSD2 isoform X2
-
XM_054350806.1 → XP_054206781.1 histone-lysine N-methyltransferase NSD2 isoform X3
- UniProtKB/TrEMBL
-
A0A7P0P278
-
XM_054350808.1 → XP_054206783.1 histone-lysine N-methyltransferase NSD2 isoform X4
- UniProtKB/TrEMBL
-
A0A7P0P278
-
XM_054350807.1 → XP_054206782.1 histone-lysine N-methyltransferase NSD2 isoform X4
- UniProtKB/TrEMBL
-
A0A7P0P278
-
XM_054350805.1 → XP_054206780.1 histone-lysine N-methyltransferase NSD2 isoform X2
-
XM_054350800.1 → XP_054206775.1 histone-lysine N-methyltransferase NSD2 isoform X1
- UniProtKB/Swiss-Prot
- A2A2T2, A2A2T3, A2A2T4, A7MCZ1, D3DVQ2, O96028, O96031, Q4VBY8, Q672J1, Q6IS00, Q86V01, Q9BZB4, Q9UI92, Q9UPR2
-
XM_054350801.1 → XP_054206776.1 histone-lysine N-methyltransferase NSD2 isoform X1
- UniProtKB/Swiss-Prot
- A2A2T2, A2A2T3, A2A2T4, A7MCZ1, D3DVQ2, O96028, O96031, Q4VBY8, Q672J1, Q6IS00, Q86V01, Q9BZB4, Q9UI92, Q9UPR2
-
XM_054350809.1 → XP_054206784.1 histone-lysine N-methyltransferase NSD2 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_014919.1: Suppressed sequence
- Description
- NM_014919.1: This RefSeq was permanently suppressed because it is a nonsense-mediated mRNA decay (NMD) candidate.
-
NM_133332.1: Suppressed sequence
- Description
- NM_133332.1: This RefSeq was permanently suppressed because it is a nonsense-mediated mRNA decay (NMD) candidate.
-
NM_133333.1: Suppressed sequence
- Description
- NM_133333.1: This RefSeq was permanently suppressed because it is a nonsense-mediated mRNA decay (NMD) candidate.
-
NM_133336.2: Suppressed sequence
- Description
- NM_133336.2: This RefSeq was permanently suppressed because currently there is insufficient support for the transcript and the protein.