Canonical Allele Identifier: CA2259229338

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727970G= , CM000679.2:g.39727970G=	GRCh38
NC_000017.10:g.37884223G= , CM000679.1:g.37884223G=	GRCh37
NC_000017.9:g.35137749G=	NCBI36
NG_007503.1:g.44831G= , LRG_724:g.44831G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3694G= MANE Select	ENSP00000269571.4:p.Ala1232=
ENST00000269571.9:c.3694G=	ENSP00000269571.4:p.Ala1232=
ENST00000406381.6:c.3604G=	ENSP00000385185.2:p.Ala1202=
ENST00000445658.6:c.2866G=	ENSP00000404047.2:p.Ala956=
ENST00000541774.5:c.3649G=	ENSP00000446466.1:p.Ala1217=
ENST00000578373.5:c.*3484G=	ENSP00000463427.1:n.*3484G=
ENST00000584450.5:c.*273G=	ENSP00000463714.1:n.*273G=
ENST00000584601.5:c.3604G=	ENSP00000462438.1:p.Ala1202=
NM_001005862.2:c.3604G= , LRG_724t1:c.3604G=	NP_001005862.1:p.Ala1202=
NM_001289936.1:c.3649G= , LRG_724t4:c.3649G=	NP_001276865.1:p.Ala1217=
NM_001289937.1:c.*273G=	NP_001276866.1:n.*273G=
NM_004448.3:c.3694G= , LRG_724t2:c.3694G=	NP_004439.2:p.Ala1232=
NR_110535.1:n.4018G=
XM_024450641.1:c.3832G=	XP_024306409.1:p.Ala1278=
XM_024450642.1:c.3787G=	XP_024306410.1:p.Ala1263=
XM_024450643.1:c.3742G=	XP_024306411.1:p.Ala1248=
NM_001005862.3:c.3604G=	NP_001005862.1:p.Ala1202=
NM_001289936.2:c.3649G=	NP_001276865.1:p.Ala1217=
NM_001289937.2:c.*273G=	NP_001276866.1:n.*273G=
NM_001382782.1:c.3604G=	NP_001369711.1:p.Ala1202=
NM_001382783.1:c.3604G=	NP_001369712.1:p.Ala1202=
NM_001382784.1:c.3811G=	NP_001369713.1:p.Ala1271=
NM_001382785.1:c.3796G=	NP_001369714.1:p.Ala1266=
NM_001382786.1:c.3775G=	NP_001369715.1:p.Ala1259=
NM_001382787.1:c.3769G=	NP_001369716.1:p.Ala1257=
NM_001382788.1:c.3724G=	NP_001369717.1:p.Ala1242=
NM_001382789.1:c.3715G=	NP_001369718.1:p.Ala1239=
NM_001382790.1:c.3691G=	NP_001369719.1:p.Ala1231=
NM_001382791.1:c.3685G=	NP_001369720.1:p.Ala1229=
NM_001382792.1:c.3658G=	NP_001369721.1:p.Ala1220=
NM_001382793.1:c.3652G=	NP_001369722.1:p.Ala1218=
NM_001382794.1:c.3652G=	NP_001369723.1:p.Ala1218=
NM_001382795.1:c.3646G=	NP_001369724.1:p.Ala1216=
NM_001382796.1:c.3607G=	NP_001369725.1:p.Ala1203=
NM_001382797.1:c.3595G=	NP_001369726.1:p.Ala1199=
NM_001382798.1:c.3538G=	NP_001369727.1:p.Ala1180=
NM_001382799.1:c.3514G=	NP_001369728.1:p.Ala1172=
NM_001382800.1:c.3508G=	NP_001369729.1:p.Ala1170=
NM_001382801.1:c.3490G=	NP_001369730.1:p.Ala1164=
NM_001382802.1:c.3436G=	NP_001369731.1:p.Ala1146=
NM_001382803.1:c.*273G=	NP_001369732.1:n.*273G=
NM_001382804.1:c.2866G=	NP_001369733.1:p.Ala956=
NM_001382805.1:c.2743G=	NP_001369734.1:p.Ala915=
NM_001382806.1:c.2656G=	NP_001369735.1:p.Ala886=
NM_004448.4:c.3694G= MANE Select	NP_004439.2:p.Ala1232=
NR_110535.2:n.3932G=