Canonical Allele Identifier: CA2259229333

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727964C= , CM000679.2:g.39727964C=	GRCh38
NC_000017.10:g.37884217C= , CM000679.1:g.37884217C=	GRCh37
NC_000017.9:g.35137743C=	NCBI36
NG_007503.1:g.44825C= , LRG_724:g.44825C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3688C= MANE Select	ENSP00000269571.4:p.Arg1230=
ENST00000269571.9:c.3688C=	ENSP00000269571.4:p.Arg1230=
ENST00000406381.6:c.3598C=	ENSP00000385185.2:p.Arg1200=
ENST00000445658.6:c.2860C=	ENSP00000404047.2:p.Arg954=
ENST00000541774.5:c.3643C=	ENSP00000446466.1:p.Arg1215=
ENST00000578373.5:c.*3478C=	ENSP00000463427.1:n.*3478C=
ENST00000584450.5:c.*267C=	ENSP00000463714.1:n.*267C=
ENST00000584601.5:c.3598C=	ENSP00000462438.1:p.Arg1200=
NM_001005862.2:c.3598C= , LRG_724t1:c.3598C=	NP_001005862.1:p.Arg1200=
NM_001289936.1:c.3643C= , LRG_724t4:c.3643C=	NP_001276865.1:p.Arg1215=
NM_001289937.1:c.*267C=	NP_001276866.1:n.*267C=
NM_004448.3:c.3688C= , LRG_724t2:c.3688C=	NP_004439.2:p.Arg1230=
NR_110535.1:n.4012C=
XM_024450641.1:c.3826C=	XP_024306409.1:p.Arg1276=
XM_024450642.1:c.3781C=	XP_024306410.1:p.Arg1261=
XM_024450643.1:c.3736C=	XP_024306411.1:p.Arg1246=
NM_001005862.3:c.3598C=	NP_001005862.1:p.Arg1200=
NM_001289936.2:c.3643C=	NP_001276865.1:p.Arg1215=
NM_001289937.2:c.*267C=	NP_001276866.1:n.*267C=
NM_001382782.1:c.3598C=	NP_001369711.1:p.Arg1200=
NM_001382783.1:c.3598C=	NP_001369712.1:p.Arg1200=
NM_001382784.1:c.3805C=	NP_001369713.1:p.Arg1269=
NM_001382785.1:c.3790C=	NP_001369714.1:p.Arg1264=
NM_001382786.1:c.3769C=	NP_001369715.1:p.Arg1257=
NM_001382787.1:c.3763C=	NP_001369716.1:p.Arg1255=
NM_001382788.1:c.3718C=	NP_001369717.1:p.Arg1240=
NM_001382789.1:c.3709C=	NP_001369718.1:p.Arg1237=
NM_001382790.1:c.3685C=	NP_001369719.1:p.Arg1229=
NM_001382791.1:c.3679C=	NP_001369720.1:p.Arg1227=
NM_001382792.1:c.3652C=	NP_001369721.1:p.Arg1218=
NM_001382793.1:c.3646C=	NP_001369722.1:p.Arg1216=
NM_001382794.1:c.3646C=	NP_001369723.1:p.Arg1216=
NM_001382795.1:c.3640C=	NP_001369724.1:p.Arg1214=
NM_001382796.1:c.3601C=	NP_001369725.1:p.Arg1201=
NM_001382797.1:c.3589C=	NP_001369726.1:p.Arg1197=
NM_001382798.1:c.3532C=	NP_001369727.1:p.Arg1178=
NM_001382799.1:c.3508C=	NP_001369728.1:p.Arg1170=
NM_001382800.1:c.3502C=	NP_001369729.1:p.Arg1168=
NM_001382801.1:c.3484C=	NP_001369730.1:p.Arg1162=
NM_001382802.1:c.3430C=	NP_001369731.1:p.Arg1144=
NM_001382803.1:c.*267C=	NP_001369732.1:n.*267C=
NM_001382804.1:c.2860C=	NP_001369733.1:p.Arg954=
NM_001382805.1:c.2737C=	NP_001369734.1:p.Arg913=
NM_001382806.1:c.2650C=	NP_001369735.1:p.Arg884=
NM_004448.4:c.3688C= MANE Select	NP_004439.2:p.Arg1230=
NR_110535.2:n.3926C=