Canonical Allele Identifier: CA2259229335

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727967G= , CM000679.2:g.39727967G=	GRCh38
NC_000017.10:g.37884220G= , CM000679.1:g.37884220G=	GRCh37
NC_000017.9:g.35137746G=	NCBI36
NG_007503.1:g.44828G= , LRG_724:g.44828G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3691G= MANE Select	ENSP00000269571.4:p.Gly1231=
ENST00000269571.9:c.3691G=	ENSP00000269571.4:p.Gly1231=
ENST00000406381.6:c.3601G=	ENSP00000385185.2:p.Gly1201=
ENST00000445658.6:c.2863G=	ENSP00000404047.2:p.Gly955=
ENST00000541774.5:c.3646G=	ENSP00000446466.1:p.Gly1216=
ENST00000578373.5:c.*3481G=	ENSP00000463427.1:n.*3481G=
ENST00000584450.5:c.*270G=	ENSP00000463714.1:n.*270G=
ENST00000584601.5:c.3601G=	ENSP00000462438.1:p.Gly1201=
NM_001005862.2:c.3601G= , LRG_724t1:c.3601G=	NP_001005862.1:p.Gly1201=
NM_001289936.1:c.3646G= , LRG_724t4:c.3646G=	NP_001276865.1:p.Gly1216=
NM_001289937.1:c.*270G=	NP_001276866.1:n.*270G=
NM_004448.3:c.3691G= , LRG_724t2:c.3691G=	NP_004439.2:p.Gly1231=
NR_110535.1:n.4015G=
XM_024450641.1:c.3829G=	XP_024306409.1:p.Gly1277=
XM_024450642.1:c.3784G=	XP_024306410.1:p.Gly1262=
XM_024450643.1:c.3739G=	XP_024306411.1:p.Gly1247=
NM_001005862.3:c.3601G=	NP_001005862.1:p.Gly1201=
NM_001289936.2:c.3646G=	NP_001276865.1:p.Gly1216=
NM_001289937.2:c.*270G=	NP_001276866.1:n.*270G=
NM_001382782.1:c.3601G=	NP_001369711.1:p.Gly1201=
NM_001382783.1:c.3601G=	NP_001369712.1:p.Gly1201=
NM_001382784.1:c.3808G=	NP_001369713.1:p.Gly1270=
NM_001382785.1:c.3793G=	NP_001369714.1:p.Gly1265=
NM_001382786.1:c.3772G=	NP_001369715.1:p.Gly1258=
NM_001382787.1:c.3766G=	NP_001369716.1:p.Gly1256=
NM_001382788.1:c.3721G=	NP_001369717.1:p.Gly1241=
NM_001382789.1:c.3712G=	NP_001369718.1:p.Gly1238=
NM_001382790.1:c.3688G=	NP_001369719.1:p.Gly1230=
NM_001382791.1:c.3682G=	NP_001369720.1:p.Gly1228=
NM_001382792.1:c.3655G=	NP_001369721.1:p.Gly1219=
NM_001382793.1:c.3649G=	NP_001369722.1:p.Gly1217=
NM_001382794.1:c.3649G=	NP_001369723.1:p.Gly1217=
NM_001382795.1:c.3643G=	NP_001369724.1:p.Gly1215=
NM_001382796.1:c.3604G=	NP_001369725.1:p.Gly1202=
NM_001382797.1:c.3592G=	NP_001369726.1:p.Gly1198=
NM_001382798.1:c.3535G=	NP_001369727.1:p.Gly1179=
NM_001382799.1:c.3511G=	NP_001369728.1:p.Gly1171=
NM_001382800.1:c.3505G=	NP_001369729.1:p.Gly1169=
NM_001382801.1:c.3487G=	NP_001369730.1:p.Gly1163=
NM_001382802.1:c.3433G=	NP_001369731.1:p.Gly1145=
NM_001382803.1:c.*270G=	NP_001369732.1:n.*270G=
NM_001382804.1:c.2863G=	NP_001369733.1:p.Gly955=
NM_001382805.1:c.2740G=	NP_001369734.1:p.Gly914=
NM_001382806.1:c.2653G=	NP_001369735.1:p.Gly885=
NM_004448.4:c.3691G= MANE Select	NP_004439.2:p.Gly1231=
NR_110535.2:n.3929G=