Canonical Allele Identifier: CA294806

Gene: NSD1

Linked Data

• ClinVar Variation Id: 159271
• ClinVar RCV Id: RCV000431725 ; RCV003231175
• dbSNP Id: rs587784076
• COSMIC: COSM1177184 ; COSM1177185
• MyVariant Identifiers: chr5:g.176637210C>T (hg19) ; chr5:g.177210209C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177210209C>T , CM000667.2:g.177210209C>T	GRCh38
NC_000005.9:g.176637210C>T , CM000667.1:g.176637210C>T	GRCh37
NC_000005.8:g.176569816C>T	NCBI36
NG_009821.1:g.82131C>T , LRG_512:g.82131C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508896.7:c.937C>T	ENSP00000423372.3:p.Arg313Ter
ENST00000347982.9:c.937C>T	ENSP00000343209.5:p.Arg313Ter
ENST00000354179.9:c.937C>T	ENSP00000346111.5:p.Arg313Ter
ENST00000508896.6:c.937C>T	ENSP00000423372.2:p.Arg313Ter
ENST00000510954.6:n.612+5917C>T
ENST00000638627.3:c.754C>T	ENSP00000492679.3:p.Arg252Ter
ENST00000685206.1:n.1393C>T
ENST00000686993.1:c.937C>T	ENSP00000510020.1:p.Arg313Ter
ENST00000687453.1:c.1501C>T	ENSP00000508426.1:p.Arg501Ter
ENST00000688613.1:n.1207C>T
ENST00000689326.1:c.1810C>T	ENSP00000509594.1:p.Arg604Ter
ENST00000689345.1:c.937C>T	ENSP00000509711.1:p.Arg313Ter
ENST00000689549.1:n.1957C>T
ENST00000439151.7:c.1810C>T MANE Select	ENSP00000395929.2:p.Arg604Ter
ENST00000638627.2:c.*903C>T	ENSP00000492679.2:n.*903C>T
ENST00000347982.8:c.1003C>T	ENSP00000343209.4:p.Arg335Ter
ENST00000354179.8:c.1003C>T	ENSP00000346111.4:p.Arg335Ter
ENST00000439151.6:c.1810C>T	ENSP00000395929.2:p.Arg604Ter
NM_022455.4:c.1810C>T , LRG_512t1:c.1810C>T	NP_071900.2:p.Arg604Ter
NM_172349.2:c.1003C>T	NP_758859.1:p.Arg335Ter
XM_005265959.1:c.1810C>T	XP_005266016.1:p.Arg604Ter
XM_005265960.1:c.1003C>T	XP_005266017.1:p.Arg335Ter
XM_005265961.1:c.1003C>T	XP_005266018.1:p.Arg335Ter
XM_011534610.1:c.1810C>T	XP_011532912.1:p.Arg604Ter
XM_011534611.1:c.1810C>T	XP_011532913.1:p.Arg604Ter
XM_011534612.1:c.1390C>T	XP_011532914.1:p.Arg464Ter
XM_011534613.1:c.754C>T	XP_011532915.1:p.Arg252Ter
XM_011534614.1:c.1810C>T	XP_011532916.1:p.Arg604Ter
XM_011534615.1:c.1810C>T	XP_011532917.1:p.Arg604Ter
XM_011534616.1:c.1810C>T	XP_011532918.1:p.Arg604Ter
NM_001365684.1:c.1003C>T	NP_001352613.1:p.Arg335Ter
XM_024446150.1:c.1810C>T	XP_024301918.1:p.Arg604Ter
XM_024446151.1:c.1810C>T	XP_024301919.1:p.Arg604Ter
XM_024446152.1:c.1810C>T	XP_024301920.1:p.Arg604Ter
XM_024446153.1:c.1810C>T	XP_024301921.1:p.Arg604Ter
XM_024446154.1:c.1390C>T	XP_024301922.1:p.Arg464Ter
XM_024446155.1:c.1003C>T	XP_024301923.1:p.Arg335Ter
XM_024446156.1:c.1003C>T	XP_024301924.1:p.Arg335Ter
XM_024446158.1:c.1003C>T	XP_024301926.1:p.Arg335Ter
XM_024446159.1:c.754C>T	XP_024301927.1:p.Arg252Ter
XM_024446160.1:c.1810C>T	XP_024301928.1:p.Arg604Ter
XM_024446161.1:c.1810C>T	XP_024301929.1:p.Arg604Ter
XM_024446162.1:c.-2186C>T	XP_024301930.1:n.-2186C>T
NM_022455.5:c.1810C>T MANE Select	NP_071900.2:p.Arg604Ter
NM_172349.3:c.1003C>T	NP_758859.1:p.Arg335Ter