Canonical Allele Identifier: CA362310326

Gene: NSD1

Linked Data

• MyVariant Identifiers: chr5:g.176636967G>T (hg19) ; chr5:g.177209966G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177209966G>T , CM000667.2:g.177209966G>T	GRCh38
NC_000005.9:g.176636967G>T , CM000667.1:g.176636967G>T	GRCh37
NC_000005.8:g.176569573G>T	NCBI36
NG_009821.1:g.81888G>T , LRG_512:g.81888G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000508896.7:c.694G>T	ENSP00000423372.3:p.Asp232Tyr
ENST00000347982.9:c.694G>T	ENSP00000343209.5:p.Asp232Tyr
ENST00000354179.9:c.694G>T	ENSP00000346111.5:p.Asp232Tyr
ENST00000508896.6:c.694G>T	ENSP00000423372.2:p.Asp232Tyr
ENST00000510954.6:n.612+5674G>T
ENST00000638627.3:c.511G>T	ENSP00000492679.3:p.Asp171Tyr
ENST00000644863.2:c.511G>T	ENSP00000496157.2:p.Asp171Tyr
ENST00000685206.1:n.1150G>T
ENST00000686993.1:c.694G>T	ENSP00000510020.1:p.Asp232Tyr
ENST00000687453.1:c.1258G>T	ENSP00000508426.1:p.Asp420Tyr
ENST00000688613.1:n.964G>T
ENST00000689326.1:c.1567G>T	ENSP00000509594.1:p.Asp523Tyr
ENST00000689345.1:c.694G>T	ENSP00000509711.1:p.Asp232Tyr
ENST00000689549.1:n.1714G>T
ENST00000439151.7:c.1567G>T MANE Select	ENSP00000395929.2:p.Asp523Tyr
ENST00000638627.2:c.*660G>T	ENSP00000492679.2:n.*660G>T
ENST00000644863.1:c.*876G>T	ENSP00000496157.1:n.*876G>T
ENST00000347982.8:c.760G>T	ENSP00000343209.4:p.Asp254Tyr
ENST00000354179.8:c.760G>T	ENSP00000346111.4:p.Asp254Tyr
ENST00000439151.6:c.1567G>T	ENSP00000395929.2:p.Asp523Tyr
NM_022455.4:c.1567G>T , LRG_512t1:c.1567G>T	NP_071900.2:p.Asp523Tyr
NM_172349.2:c.760G>T	NP_758859.1:p.Asp254Tyr
XM_005265959.1:c.1567G>T	XP_005266016.1:p.Asp523Tyr
XM_005265960.1:c.760G>T	XP_005266017.1:p.Asp254Tyr
XM_005265961.1:c.760G>T	XP_005266018.1:p.Asp254Tyr
XM_011534610.1:c.1567G>T	XP_011532912.1:p.Asp523Tyr
XM_011534611.1:c.1567G>T	XP_011532913.1:p.Asp523Tyr
XM_011534612.1:c.1147G>T	XP_011532914.1:p.Asp383Tyr
XM_011534613.1:c.511G>T	XP_011532915.1:p.Asp171Tyr
XM_011534614.1:c.1567G>T	XP_011532916.1:p.Asp523Tyr
XM_011534615.1:c.1567G>T	XP_011532917.1:p.Asp523Tyr
XM_011534616.1:c.1567G>T	XP_011532918.1:p.Asp523Tyr
NM_001365684.1:c.760G>T	NP_001352613.1:p.Asp254Tyr
XM_024446150.1:c.1567G>T	XP_024301918.1:p.Asp523Tyr
XM_024446151.1:c.1567G>T	XP_024301919.1:p.Asp523Tyr
XM_024446152.1:c.1567G>T	XP_024301920.1:p.Asp523Tyr
XM_024446153.1:c.1567G>T	XP_024301921.1:p.Asp523Tyr
XM_024446154.1:c.1147G>T	XP_024301922.1:p.Asp383Tyr
XM_024446155.1:c.760G>T	XP_024301923.1:p.Asp254Tyr
XM_024446156.1:c.760G>T	XP_024301924.1:p.Asp254Tyr
XM_024446158.1:c.760G>T	XP_024301926.1:p.Asp254Tyr
XM_024446159.1:c.511G>T	XP_024301927.1:p.Asp171Tyr
XM_024446160.1:c.1567G>T	XP_024301928.1:p.Asp523Tyr
XM_024446161.1:c.1567G>T	XP_024301929.1:p.Asp523Tyr
XM_024446162.1:c.-2429G>T	XP_024301930.1:n.-2429G>T
NM_022455.5:c.1567G>T MANE Select	NP_071900.2:p.Asp523Tyr
NM_172349.3:c.760G>T	NP_758859.1:p.Asp254Tyr