Canonical Allele Identifier: CA2259229325

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727941A= , CM000679.2:g.39727941A=	GRCh38
NC_000017.10:g.37884194A= , CM000679.1:g.37884194A=	GRCh37
NC_000017.9:g.35137720A=	NCBI36
NG_007503.1:g.44802A= , LRG_724:g.44802A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3665A= MANE Select	ENSP00000269571.4:p.Tyr1222=
ENST00000269571.9:c.3665A=	ENSP00000269571.4:p.Tyr1222=
ENST00000406381.6:c.3575A=	ENSP00000385185.2:p.Tyr1192=
ENST00000445658.6:c.2837A=	ENSP00000404047.2:p.Tyr946=
ENST00000541774.5:c.3620A=	ENSP00000446466.1:p.Tyr1207=
ENST00000578373.5:c.*3455A=	ENSP00000463427.1:n.*3455A=
ENST00000584450.5:c.*244A=	ENSP00000463714.1:n.*244A=
ENST00000584601.5:c.3575A=	ENSP00000462438.1:p.Tyr1192=
NM_001005862.2:c.3575A= , LRG_724t1:c.3575A=	NP_001005862.1:p.Tyr1192=
NM_001289936.1:c.3620A= , LRG_724t4:c.3620A=	NP_001276865.1:p.Tyr1207=
NM_001289937.1:c.*244A=	NP_001276866.1:n.*244A=
NM_004448.3:c.3665A= , LRG_724t2:c.3665A=	NP_004439.2:p.Tyr1222=
NR_110535.1:n.3989A=
XM_024450641.1:c.3803A=	XP_024306409.1:p.Tyr1268=
XM_024450642.1:c.3758A=	XP_024306410.1:p.Tyr1253=
XM_024450643.1:c.3713A=	XP_024306411.1:p.Tyr1238=
NM_001005862.3:c.3575A=	NP_001005862.1:p.Tyr1192=
NM_001289936.2:c.3620A=	NP_001276865.1:p.Tyr1207=
NM_001289937.2:c.*244A=	NP_001276866.1:n.*244A=
NM_001382782.1:c.3575A=	NP_001369711.1:p.Tyr1192=
NM_001382783.1:c.3575A=	NP_001369712.1:p.Tyr1192=
NM_001382784.1:c.3782A=	NP_001369713.1:p.Tyr1261=
NM_001382785.1:c.3767A=	NP_001369714.1:p.Tyr1256=
NM_001382786.1:c.3746A=	NP_001369715.1:p.Tyr1249=
NM_001382787.1:c.3740A=	NP_001369716.1:p.Tyr1247=
NM_001382788.1:c.3695A=	NP_001369717.1:p.Tyr1232=
NM_001382789.1:c.3686A=	NP_001369718.1:p.Tyr1229=
NM_001382790.1:c.3662A=	NP_001369719.1:p.Tyr1221=
NM_001382791.1:c.3656A=	NP_001369720.1:p.Tyr1219=
NM_001382792.1:c.3629A=	NP_001369721.1:p.Tyr1210=
NM_001382793.1:c.3623A=	NP_001369722.1:p.Tyr1208=
NM_001382794.1:c.3623A=	NP_001369723.1:p.Tyr1208=
NM_001382795.1:c.3617A=	NP_001369724.1:p.Tyr1206=
NM_001382796.1:c.3578A=	NP_001369725.1:p.Tyr1193=
NM_001382797.1:c.3566A=	NP_001369726.1:p.Tyr1189=
NM_001382798.1:c.3509A=	NP_001369727.1:p.Tyr1170=
NM_001382799.1:c.3485A=	NP_001369728.1:p.Tyr1162=
NM_001382800.1:c.3479A=	NP_001369729.1:p.Tyr1160=
NM_001382801.1:c.3461A=	NP_001369730.1:p.Tyr1154=
NM_001382802.1:c.3407A=	NP_001369731.1:p.Tyr1136=
NM_001382803.1:c.*244A=	NP_001369732.1:n.*244A=
NM_001382804.1:c.2837A=	NP_001369733.1:p.Tyr946=
NM_001382805.1:c.2714A=	NP_001369734.1:p.Tyr905=
NM_001382806.1:c.2627A=	NP_001369735.1:p.Tyr876=
NM_004448.4:c.3665A= MANE Select	NP_004439.2:p.Tyr1222=
NR_110535.2:n.3903A=