Canonical Allele Identifier: CA2259228003

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724779C= , CM000679.2:g.39724779C=	GRCh38
NC_000017.10:g.37881032C= , CM000679.1:g.37881032C=	GRCh37
NC_000017.9:g.35134558C=	NCBI36
NG_007503.1:g.41640C= , LRG_724:g.41640C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2361C= MANE Select	ENSP00000269571.4:p.Gly787=
ENST00000269571.9:c.2361C=	ENSP00000269571.4:p.Gly787=
ENST00000406381.6:c.2271C=	ENSP00000385185.2:p.Gly757=
ENST00000445658.6:c.1533C=	ENSP00000404047.2:p.Gly511=
ENST00000541774.5:c.2316C=	ENSP00000446466.1:p.Gly772=
ENST00000578373.5:c.*2151C=	ENSP00000463427.1:n.*2151C=
ENST00000580074.1:c.467C=
ENST00000583038.5:n.3495C=
ENST00000584450.5:c.2361C=	ENSP00000463714.1:p.Gly787=
ENST00000584601.5:c.2271C=	ENSP00000462438.1:p.Gly757=
NM_001005862.2:c.2271C= , LRG_724t1:c.2271C=	NP_001005862.1:p.Gly757=
NM_001289936.1:c.2316C= , LRG_724t4:c.2316C=	NP_001276865.1:p.Gly772=
NM_001289937.1:c.2361C=	NP_001276866.1:p.Gly787=
NM_004448.3:c.2361C= , LRG_724t2:c.2361C=	NP_004439.2:p.Gly787=
NR_110535.1:n.2685C=
XM_024450641.1:c.2499C=	XP_024306409.1:p.Gly833=
XM_024450642.1:c.2454C=	XP_024306410.1:p.Gly818=
XM_024450643.1:c.2409C=	XP_024306411.1:p.Gly803=
NM_001005862.3:c.2271C=	NP_001005862.1:p.Gly757=
NM_001289936.2:c.2316C=	NP_001276865.1:p.Gly772=
NM_001289937.2:c.2361C=	NP_001276866.1:p.Gly787=
NM_001382782.1:c.2271C=	NP_001369711.1:p.Gly757=
NM_001382783.1:c.2271C=	NP_001369712.1:p.Gly757=
NM_001382784.1:c.2478C=	NP_001369713.1:p.Gly826=
NM_001382785.1:c.2463C=	NP_001369714.1:p.Gly821=
NM_001382786.1:c.2442C=	NP_001369715.1:p.Gly814=
NM_001382787.1:c.2436C=	NP_001369716.1:p.Gly812=
NM_001382788.1:c.2391C=	NP_001369717.1:p.Gly797=
NM_001382789.1:c.2382C=	NP_001369718.1:p.Gly794=
NM_001382790.1:c.2358C=	NP_001369719.1:p.Gly786=
NM_001382791.1:c.2352C=	NP_001369720.1:p.Gly784=
NM_001382792.1:c.2325C=	NP_001369721.1:p.Gly775=
NM_001382793.1:c.2319C=	NP_001369722.1:p.Gly773=
NM_001382794.1:c.2319C=	NP_001369723.1:p.Gly773=
NM_001382795.1:c.2313C=	NP_001369724.1:p.Gly771=
NM_001382796.1:c.2361C=	NP_001369725.1:p.Gly787=
NM_001382797.1:c.2262C=	NP_001369726.1:p.Gly754=
NM_001382798.1:c.2361C=	NP_001369727.1:p.Gly787=
NM_001382799.1:c.2181C=	NP_001369728.1:p.Gly727=
NM_001382800.1:c.2308-270C=	NP_001369729.1:n.2308-270C=
NM_001382801.1:c.2313C=	NP_001369730.1:p.Gly771=
NM_001382802.1:c.2103C=	NP_001369731.1:p.Gly701=
NM_001382803.1:c.2319C=	NP_001369732.1:p.Gly773=
NM_001382804.1:c.1533C=	NP_001369733.1:p.Gly511=
NM_001382805.1:c.2208+1119C=	NP_001369734.1:n.2208+1119C=
NM_001382806.1:c.1323C=	NP_001369735.1:p.Gly441=
NM_004448.4:c.2361C= MANE Select	NP_004439.2:p.Gly787=
NR_110535.2:n.2599C=