Canonical Allele Identifier: CA16611845
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 407360
ClinVar RCV Id: RCV003231622
dbSNP Id: rs1060501490

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177211018_177211022del , CM000667.2:g.177211018_177211022del GRCh38
NC_000005.9:g.176638019_176638023del , CM000667.1:g.176638019_176638023del GRCh37
NC_000005.8:g.176570625_176570629del NCBI36
NG_009821.1:g.82940_82944del , LRG_512:g.82940_82944del

Transcript Alleles

HGVS Amino-acid change
ENST00000508896.7:c.1746_1750del ENSP00000423372.3:p.Glu583CysfsTer3
ENST00000347982.9:c.1746_1750del ENSP00000343209.5:p.Glu583CysfsTer3
ENST00000354179.9:c.1746_1750del ENSP00000346111.5:p.Glu583CysfsTer3
ENST00000510954.6:n.612+6726_612+6730del
ENST00000685206.1:n.2202_2206del
ENST00000686993.1:c.1746_1750del ENSP00000510020.1:p.Glu583CysfsTer3
ENST00000687453.1:c.2310_2314del ENSP00000508426.1:p.Glu771CysfsTer3
ENST00000688613.1:n.2016_2020del
ENST00000689326.1:c.2619_2623del ENSP00000509594.1:p.Glu874CysfsTer3
ENST00000689345.1:c.1746_1750del ENSP00000509711.1:p.Glu583CysfsTer3
ENST00000689549.1:n.2766_2770del
ENST00000439151.7:c.2619_2623del MANE Select ENSP00000395929.2:p.Glu874CysfsTer3
ENST00000347982.8:c.1812_1816del ENSP00000343209.4:p.Glu605CysfsTer3
ENST00000354179.8:c.1812_1816del ENSP00000346111.4:p.Glu605CysfsTer3
ENST00000439151.6:c.2619_2623del ENSP00000395929.2:p.Glu874CysfsTer3
NM_022455.4:c.2619_2623del , LRG_512t1:c.2619_2623del NP_071900.2:p.Glu874CysfsTer3
NM_172349.2:c.1812_1816del NP_758859.1:p.Glu605CysfsTer3
XM_005265959.1:c.2619_2623del XP_005266016.1:p.Glu874CysfsTer3
XM_005265960.1:c.1812_1816del XP_005266017.1:p.Glu605CysfsTer3
XM_005265961.1:c.1812_1816del XP_005266018.1:p.Glu605CysfsTer3
XM_011534610.1:c.2619_2623del XP_011532912.1:p.Glu874CysfsTer3
XM_011534611.1:c.2619_2623del XP_011532913.1:p.Glu874CysfsTer3
XM_011534612.1:c.2199_2203del XP_011532914.1:p.Glu734CysfsTer3
XM_011534613.1:c.1563_1567del XP_011532915.1:p.Glu522CysfsTer3
XM_011534614.1:c.2619_2623del XP_011532916.1:p.Glu874CysfsTer3
XM_011534615.1:c.2619_2623del XP_011532917.1:p.Glu874CysfsTer3
XM_011534616.1:c.2619_2623del XP_011532918.1:p.Glu874CysfsTer3
NM_001365684.1:c.1812_1816del NP_001352613.1:p.Glu605CysfsTer3
XM_024446150.1:c.2619_2623del XP_024301918.1:p.Glu874CysfsTer3
XM_024446151.1:c.2619_2623del XP_024301919.1:p.Glu874CysfsTer3
XM_024446152.1:c.2619_2623del XP_024301920.1:p.Glu874CysfsTer3
XM_024446153.1:c.2619_2623del XP_024301921.1:p.Glu874CysfsTer3
XM_024446154.1:c.2199_2203del XP_024301922.1:p.Glu734CysfsTer3
XM_024446155.1:c.1812_1816del XP_024301923.1:p.Glu605CysfsTer3
XM_024446156.1:c.1812_1816del XP_024301924.1:p.Glu605CysfsTer3
XM_024446158.1:c.1812_1816del XP_024301926.1:p.Glu605CysfsTer3
XM_024446159.1:c.1563_1567del XP_024301927.1:p.Glu522CysfsTer3
XM_024446160.1:c.2619_2623del XP_024301928.1:p.Glu874CysfsTer3
XM_024446161.1:c.2619_2623del XP_024301929.1:p.Glu874CysfsTer3
XM_024446162.1:c.-1377_-1373del XP_024301930.1:n.-1377_-1373del
NM_022455.5:c.2619_2623del MANE Select NP_071900.2:p.Glu874CysfsTer3
NM_172349.3:c.1812_1816del NP_758859.1:p.Glu605CysfsTer3