Canonical Allele Identifier: CA399314490

Gene: ERBB2

Linked Data

• dbSNP Id: rs2059872380
• MyVariant Identifiers: chr17:g.37884206A>T (hg19) ; chr17:g.39727953A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727953A>T , CM000679.2:g.39727953A>T	GRCh38
NC_000017.10:g.37884206A>T , CM000679.1:g.37884206A>T	GRCh37
NC_000017.9:g.35137732A>T	NCBI36
NG_007503.1:g.44814A>T , LRG_724:g.44814A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3677A>T MANE Select	ENSP00000269571.4:p.Asp1226Val
ENST00000269571.9:c.3677A>T	ENSP00000269571.4:p.Asp1226Val
ENST00000406381.6:c.3587A>T	ENSP00000385185.2:p.Asp1196Val
ENST00000445658.6:c.2849A>T	ENSP00000404047.2:p.Asp950Val
ENST00000541774.5:c.3632A>T	ENSP00000446466.1:p.Asp1211Val
ENST00000578373.5:c.*3467A>T	ENSP00000463427.1:n.*3467A>T
ENST00000584450.5:c.*256A>T	ENSP00000463714.1:n.*256A>T
ENST00000584601.5:c.3587A>T	ENSP00000462438.1:p.Asp1196Val
NM_001005862.2:c.3587A>T , LRG_724t1:c.3587A>T	NP_001005862.1:p.Asp1196Val
NM_001289936.1:c.3632A>T , LRG_724t4:c.3632A>T	NP_001276865.1:p.Asp1211Val
NM_001289937.1:c.*256A>T	NP_001276866.1:n.*256A>T
NM_004448.3:c.3677A>T , LRG_724t2:c.3677A>T	NP_004439.2:p.Asp1226Val
NR_110535.1:n.4001A>T
XM_024450641.1:c.3815A>T	XP_024306409.1:p.Asp1272Val
XM_024450642.1:c.3770A>T	XP_024306410.1:p.Asp1257Val
XM_024450643.1:c.3725A>T	XP_024306411.1:p.Asp1242Val
NM_001005862.3:c.3587A>T	NP_001005862.1:p.Asp1196Val
NM_001289936.2:c.3632A>T	NP_001276865.1:p.Asp1211Val
NM_001289937.2:c.*256A>T	NP_001276866.1:n.*256A>T
NM_001382782.1:c.3587A>T	NP_001369711.1:p.Asp1196Val
NM_001382783.1:c.3587A>T	NP_001369712.1:p.Asp1196Val
NM_001382784.1:c.3794A>T	NP_001369713.1:p.Asp1265Val
NM_001382785.1:c.3779A>T	NP_001369714.1:p.Asp1260Val
NM_001382786.1:c.3758A>T	NP_001369715.1:p.Asp1253Val
NM_001382787.1:c.3752A>T	NP_001369716.1:p.Asp1251Val
NM_001382788.1:c.3707A>T	NP_001369717.1:p.Asp1236Val
NM_001382789.1:c.3698A>T	NP_001369718.1:p.Asp1233Val
NM_001382790.1:c.3674A>T	NP_001369719.1:p.Asp1225Val
NM_001382791.1:c.3668A>T	NP_001369720.1:p.Asp1223Val
NM_001382792.1:c.3641A>T	NP_001369721.1:p.Asp1214Val
NM_001382793.1:c.3635A>T	NP_001369722.1:p.Asp1212Val
NM_001382794.1:c.3635A>T	NP_001369723.1:p.Asp1212Val
NM_001382795.1:c.3629A>T	NP_001369724.1:p.Asp1210Val
NM_001382796.1:c.3590A>T	NP_001369725.1:p.Asp1197Val
NM_001382797.1:c.3578A>T	NP_001369726.1:p.Asp1193Val
NM_001382798.1:c.3521A>T	NP_001369727.1:p.Asp1174Val
NM_001382799.1:c.3497A>T	NP_001369728.1:p.Asp1166Val
NM_001382800.1:c.3491A>T	NP_001369729.1:p.Asp1164Val
NM_001382801.1:c.3473A>T	NP_001369730.1:p.Asp1158Val
NM_001382802.1:c.3419A>T	NP_001369731.1:p.Asp1140Val
NM_001382803.1:c.*256A>T	NP_001369732.1:n.*256A>T
NM_001382804.1:c.2849A>T	NP_001369733.1:p.Asp950Val
NM_001382805.1:c.2726A>T	NP_001369734.1:p.Asp909Val
NM_001382806.1:c.2639A>T	NP_001369735.1:p.Asp880Val
NM_004448.4:c.3677A>T MANE Select	NP_004439.2:p.Asp1226Val
NR_110535.2:n.3915A>T