Canonical Allele Identifier: CA2259229315

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727911C= , CM000679.2:g.39727911C=	GRCh38
NC_000017.10:g.37884164C= , CM000679.1:g.37884164C=	GRCh37
NC_000017.9:g.35137690C=	NCBI36
NG_007503.1:g.44772C= , LRG_724:g.44772C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3635C= MANE Select	ENSP00000269571.4:p.Ala1212=
ENST00000269571.9:c.3635C=	ENSP00000269571.4:p.Ala1212=
ENST00000406381.6:c.3545C=	ENSP00000385185.2:p.Ala1182=
ENST00000445658.6:c.2807C=	ENSP00000404047.2:p.Ala936=
ENST00000541774.5:c.3590C=	ENSP00000446466.1:p.Ala1197=
ENST00000578373.5:c.*3425C=	ENSP00000463427.1:n.*3425C=
ENST00000584450.5:c.*214C=	ENSP00000463714.1:n.*214C=
ENST00000584601.5:c.3545C=	ENSP00000462438.1:p.Ala1182=
NM_001005862.2:c.3545C= , LRG_724t1:c.3545C=	NP_001005862.1:p.Ala1182=
NM_001289936.1:c.3590C= , LRG_724t4:c.3590C=	NP_001276865.1:p.Ala1197=
NM_001289937.1:c.*214C=	NP_001276866.1:n.*214C=
NM_004448.3:c.3635C= , LRG_724t2:c.3635C=	NP_004439.2:p.Ala1212=
NR_110535.1:n.3959C=
XM_024450641.1:c.3773C=	XP_024306409.1:p.Ala1258=
XM_024450642.1:c.3728C=	XP_024306410.1:p.Ala1243=
XM_024450643.1:c.3683C=	XP_024306411.1:p.Ala1228=
NM_001005862.3:c.3545C=	NP_001005862.1:p.Ala1182=
NM_001289936.2:c.3590C=	NP_001276865.1:p.Ala1197=
NM_001289937.2:c.*214C=	NP_001276866.1:n.*214C=
NM_001382782.1:c.3545C=	NP_001369711.1:p.Ala1182=
NM_001382783.1:c.3545C=	NP_001369712.1:p.Ala1182=
NM_001382784.1:c.3752C=	NP_001369713.1:p.Ala1251=
NM_001382785.1:c.3737C=	NP_001369714.1:p.Ala1246=
NM_001382786.1:c.3716C=	NP_001369715.1:p.Ala1239=
NM_001382787.1:c.3710C=	NP_001369716.1:p.Ala1237=
NM_001382788.1:c.3665C=	NP_001369717.1:p.Ala1222=
NM_001382789.1:c.3656C=	NP_001369718.1:p.Ala1219=
NM_001382790.1:c.3632C=	NP_001369719.1:p.Ala1211=
NM_001382791.1:c.3626C=	NP_001369720.1:p.Ala1209=
NM_001382792.1:c.3599C=	NP_001369721.1:p.Ala1200=
NM_001382793.1:c.3593C=	NP_001369722.1:p.Ala1198=
NM_001382794.1:c.3593C=	NP_001369723.1:p.Ala1198=
NM_001382795.1:c.3587C=	NP_001369724.1:p.Ala1196=
NM_001382796.1:c.3548C=	NP_001369725.1:p.Ala1183=
NM_001382797.1:c.3536C=	NP_001369726.1:p.Ala1179=
NM_001382798.1:c.3479C=	NP_001369727.1:p.Ala1160=
NM_001382799.1:c.3455C=	NP_001369728.1:p.Ala1152=
NM_001382800.1:c.3449C=	NP_001369729.1:p.Ala1150=
NM_001382801.1:c.3431C=	NP_001369730.1:p.Ala1144=
NM_001382802.1:c.3377C=	NP_001369731.1:p.Ala1126=
NM_001382803.1:c.*214C=	NP_001369732.1:n.*214C=
NM_001382804.1:c.2807C=	NP_001369733.1:p.Ala936=
NM_001382805.1:c.2684C=	NP_001369734.1:p.Ala895=
NM_001382806.1:c.2597C=	NP_001369735.1:p.Ala866=
NM_004448.4:c.3635C= MANE Select	NP_004439.2:p.Ala1212=
NR_110535.2:n.3873C=