Canonical Allele Identifier: CA2259228832

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727480C= , CM000679.2:g.39727480C=	GRCh38
NC_000017.10:g.37883733C= , CM000679.1:g.37883733C=	GRCh37
NC_000017.9:g.35137259C=	NCBI36
NG_007503.1:g.44341C= , LRG_724:g.44341C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3345C= MANE Select	ENSP00000269571.4:p.Asp1115=
ENST00000269571.9:c.3345C=	ENSP00000269571.4:p.Asp1115=
ENST00000406381.6:c.3255C=	ENSP00000385185.2:p.Asp1085=
ENST00000445658.6:c.2517C=	ENSP00000404047.2:p.Asp839=
ENST00000541774.5:c.3300C=	ENSP00000446466.1:p.Asp1100=
ENST00000578373.5:c.*3135C=	ENSP00000463427.1:n.*3135C=
ENST00000584450.5:c.3160-209C=	ENSP00000463714.1:n.3160-209C=
ENST00000584601.5:c.3255C=	ENSP00000462438.1:p.Asp1085=
NM_001005862.2:c.3255C= , LRG_724t1:c.3255C=	NP_001005862.1:p.Asp1085=
NM_001289936.1:c.3300C= , LRG_724t4:c.3300C=	NP_001276865.1:p.Asp1100=
NM_001289937.1:c.3160-209C=	NP_001276866.1:n.3160-209C=
NM_004448.3:c.3345C= , LRG_724t2:c.3345C=	NP_004439.2:p.Asp1115=
NR_110535.1:n.3669C=
XM_024450641.1:c.3483C=	XP_024306409.1:p.Asp1161=
XM_024450642.1:c.3438C=	XP_024306410.1:p.Asp1146=
XM_024450643.1:c.3393C=	XP_024306411.1:p.Asp1131=
NM_001005862.3:c.3255C=	NP_001005862.1:p.Asp1085=
NM_001289936.2:c.3300C=	NP_001276865.1:p.Asp1100=
NM_001289937.2:c.3160-209C=	NP_001276866.1:n.3160-209C=
NM_001382782.1:c.3255C=	NP_001369711.1:p.Asp1085=
NM_001382783.1:c.3255C=	NP_001369712.1:p.Asp1085=
NM_001382784.1:c.3462C=	NP_001369713.1:p.Asp1154=
NM_001382785.1:c.3447C=	NP_001369714.1:p.Asp1149=
NM_001382786.1:c.3426C=	NP_001369715.1:p.Asp1142=
NM_001382787.1:c.3420C=	NP_001369716.1:p.Asp1140=
NM_001382788.1:c.3375C=	NP_001369717.1:p.Asp1125=
NM_001382789.1:c.3366C=	NP_001369718.1:p.Asp1122=
NM_001382790.1:c.3342C=	NP_001369719.1:p.Asp1114=
NM_001382791.1:c.3336C=	NP_001369720.1:p.Asp1112=
NM_001382792.1:c.3309C=	NP_001369721.1:p.Asp1103=
NM_001382793.1:c.3303C=	NP_001369722.1:p.Asp1101=
NM_001382794.1:c.3303C=	NP_001369723.1:p.Asp1101=
NM_001382795.1:c.3297C=	NP_001369724.1:p.Asp1099=
NM_001382796.1:c.3258C=	NP_001369725.1:p.Asp1086=
NM_001382797.1:c.3246C=	NP_001369726.1:p.Asp1082=
NM_001382798.1:c.3189C=	NP_001369727.1:p.Asp1063=
NM_001382799.1:c.3165C=	NP_001369728.1:p.Asp1055=
NM_001382800.1:c.3159C=	NP_001369729.1:p.Asp1053=
NM_001382801.1:c.3141C=	NP_001369730.1:p.Asp1047=
NM_001382802.1:c.3087C=	NP_001369731.1:p.Asp1029=
NM_001382803.1:c.3118-209C=	NP_001369732.1:n.3118-209C=
NM_001382804.1:c.2517C=	NP_001369733.1:p.Asp839=
NM_001382805.1:c.2394C=	NP_001369734.1:p.Asp798=
NM_001382806.1:c.2307C=	NP_001369735.1:p.Asp769=
NM_004448.4:c.3345C= MANE Select	NP_004439.2:p.Asp1115=
NR_110535.2:n.3583C=