Canonical Allele Identifier: CA2259229331

Gene: ERBB2

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3677A= MANE Select	ENSP00000269571.4:p.Asp1226=
ENST00000269571.9:c.3677A=	ENSP00000269571.4:p.Asp1226=
ENST00000406381.6:c.3587A=	ENSP00000385185.2:p.Asp1196=
ENST00000445658.6:c.2849A=	ENSP00000404047.2:p.Asp950=
ENST00000541774.5:c.3632A=	ENSP00000446466.1:p.Asp1211=
ENST00000578373.5:c.*3467A=	ENSP00000463427.1:n.*3467A=
ENST00000584450.5:c.*256A=	ENSP00000463714.1:n.*256A=
ENST00000584601.5:c.3587A=	ENSP00000462438.1:p.Asp1196=
NM_001005862.2:c.3587A= , LRG_724t1:c.3587A=	NP_001005862.1:p.Asp1196=
NM_001289936.1:c.3632A= , LRG_724t4:c.3632A=	NP_001276865.1:p.Asp1211=
NM_001289937.1:c.*256A=	NP_001276866.1:n.*256A=
NM_004448.3:c.3677A= , LRG_724t2:c.3677A=	NP_004439.2:p.Asp1226=
NR_110535.1:n.4001A=
XM_024450641.1:c.3815A=	XP_024306409.1:p.Asp1272=
XM_024450642.1:c.3770A=	XP_024306410.1:p.Asp1257=
XM_024450643.1:c.3725A=	XP_024306411.1:p.Asp1242=
NM_001005862.3:c.3587A=	NP_001005862.1:p.Asp1196=
NM_001289936.2:c.3632A=	NP_001276865.1:p.Asp1211=
NM_001289937.2:c.*256A=	NP_001276866.1:n.*256A=
NM_001382782.1:c.3587A=	NP_001369711.1:p.Asp1196=
NM_001382783.1:c.3587A=	NP_001369712.1:p.Asp1196=
NM_001382784.1:c.3794A=	NP_001369713.1:p.Asp1265=
NM_001382785.1:c.3779A=	NP_001369714.1:p.Asp1260=
NM_001382786.1:c.3758A=	NP_001369715.1:p.Asp1253=
NM_001382787.1:c.3752A=	NP_001369716.1:p.Asp1251=
NM_001382788.1:c.3707A=	NP_001369717.1:p.Asp1236=
NM_001382789.1:c.3698A=	NP_001369718.1:p.Asp1233=
NM_001382790.1:c.3674A=	NP_001369719.1:p.Asp1225=
NM_001382791.1:c.3668A=	NP_001369720.1:p.Asp1223=
NM_001382792.1:c.3641A=	NP_001369721.1:p.Asp1214=
NM_001382793.1:c.3635A=	NP_001369722.1:p.Asp1212=
NM_001382794.1:c.3635A=	NP_001369723.1:p.Asp1212=
NM_001382795.1:c.3629A=	NP_001369724.1:p.Asp1210=
NM_001382796.1:c.3590A=	NP_001369725.1:p.Asp1197=
NM_001382797.1:c.3578A=	NP_001369726.1:p.Asp1193=
NM_001382798.1:c.3521A=	NP_001369727.1:p.Asp1174=
NM_001382799.1:c.3497A=	NP_001369728.1:p.Asp1166=
NM_001382800.1:c.3491A=	NP_001369729.1:p.Asp1164=
NM_001382801.1:c.3473A=	NP_001369730.1:p.Asp1158=
NM_001382802.1:c.3419A=	NP_001369731.1:p.Asp1140=
NM_001382803.1:c.*256A=	NP_001369732.1:n.*256A=
NM_001382804.1:c.2849A=	NP_001369733.1:p.Asp950=
NM_001382805.1:c.2726A=	NP_001369734.1:p.Asp909=
NM_001382806.1:c.2639A=	NP_001369735.1:p.Asp880=
NM_004448.4:c.3677A= MANE Select	NP_004439.2:p.Asp1226=
NR_110535.2:n.3915A=