Canonical Allele Identifier: CA319737
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 211742
ClinVar RCV Id: RCV003231396
dbSNP Id: rs797045829

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177291985dup , CM000667.2:g.177291985dup GRCh38
NC_000005.9:g.176718986dup , CM000667.1:g.176718986dup GRCh37
NC_000005.8:g.176651592dup NCBI36
NG_009821.1:g.163907dup , LRG_512:g.163907dup

Transcript Alleles

HGVS Amino-acid change
ENST00000508896.7:c.5417dup ENSP00000423372.3:p.Lys1807GlufsTer15
ENST00000347982.9:c.5417dup ENSP00000343209.5:p.Lys1807GlufsTer15
ENST00000354179.9:c.5417dup ENSP00000346111.5:p.Lys1807GlufsTer15
ENST00000503056.6:c.932dup ENSP00000424024.2:p.Lys312GlufsTer15
ENST00000508029.6:c.932dup ENSP00000425120.2:p.Lys312GlufsTer15
ENST00000685206.1:n.5873dup
ENST00000686385.1:n.706dup
ENST00000686993.1:c.5417dup ENSP00000510020.1:p.Lys1807GlufsTer15
ENST00000687453.1:c.5981dup ENSP00000508426.1:p.Lys1995GlufsTer15
ENST00000688613.1:n.5687dup
ENST00000689345.1:c.5417dup ENSP00000509711.1:p.Lys1807GlufsTer15
ENST00000439151.7:c.6290dup MANE Select ENSP00000395929.2:p.Lys2098GlufsTer15
ENST00000347982.8:c.5483dup ENSP00000343209.4:p.Lys1829GlufsTer15
ENST00000354179.8:c.5483dup ENSP00000346111.4:p.Lys1829GlufsTer15
ENST00000439151.6:c.6290dup ENSP00000395929.2:p.Lys2098GlufsTer15
ENST00000513736.1:n.432dup
NM_022455.4:c.6290dup , LRG_512t1:c.6290dup NP_071900.2:p.Lys2098GlufsTer15
NM_172349.2:c.5483dup NP_758859.1:p.Lys1829GlufsTer15
XM_005265959.1:c.6290dup XP_005266016.1:p.Lys2098GlufsTer15
XM_005265960.1:c.5483dup XP_005266017.1:p.Lys1829GlufsTer15
XM_005265961.1:c.5483dup XP_005266018.1:p.Lys1829GlufsTer15
XM_005265962.3:c.1784dup XP_005266019.1:p.Lys596GlufsTer15
XM_011534610.1:c.6290dup XP_011532912.1:p.Lys2098GlufsTer15
XM_011534611.1:c.6290dup XP_011532913.1:p.Lys2098GlufsTer15
XM_011534612.1:c.5870dup XP_011532914.1:p.Lys1958GlufsTer15
XM_011534613.1:c.5234dup XP_011532915.1:p.Lys1746GlufsTer15
XM_011534617.1:c.2024dup XP_011532919.1:p.Lys676GlufsTer15
NM_001365684.1:c.5483dup NP_001352613.1:p.Lys1829GlufsTer15
XM_024446150.1:c.6290dup XP_024301918.1:p.Lys2098GlufsTer15
XM_024446151.1:c.6290dup XP_024301919.1:p.Lys2098GlufsTer15
XM_024446152.1:c.6290dup XP_024301920.1:p.Lys2098GlufsTer15
XM_024446153.1:c.6290dup XP_024301921.1:p.Lys2098GlufsTer15
XM_024446154.1:c.5870dup XP_024301922.1:p.Lys1958GlufsTer15
XM_024446155.1:c.5483dup XP_024301923.1:p.Lys1829GlufsTer15
XM_024446156.1:c.5483dup XP_024301924.1:p.Lys1829GlufsTer15
XM_024446158.1:c.5483dup XP_024301926.1:p.Lys1829GlufsTer15
XM_024446159.1:c.5234dup XP_024301927.1:p.Lys1746GlufsTer15
XM_024446162.1:c.2024dup XP_024301930.1:p.Lys676GlufsTer15
XM_024446163.1:c.1784dup XP_024301931.1:p.Lys596GlufsTer15
NM_022455.5:c.6290dup MANE Select NP_071900.2:p.Lys2098GlufsTer15
NM_172349.3:c.5483dup NP_758859.1:p.Lys1829GlufsTer15