Canonical Allele Identifier: CA2259229334

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727965G= , CM000679.2:g.39727965G=	GRCh38
NC_000017.10:g.37884218G= , CM000679.1:g.37884218G=	GRCh37
NC_000017.9:g.35137744G=	NCBI36
NG_007503.1:g.44826G= , LRG_724:g.44826G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3689G= MANE Select	ENSP00000269571.4:p.Arg1230=
ENST00000269571.9:c.3689G=	ENSP00000269571.4:p.Arg1230=
ENST00000406381.6:c.3599G=	ENSP00000385185.2:p.Arg1200=
ENST00000445658.6:c.2861G=	ENSP00000404047.2:p.Arg954=
ENST00000541774.5:c.3644G=	ENSP00000446466.1:p.Arg1215=
ENST00000578373.5:c.*3479G=	ENSP00000463427.1:n.*3479G=
ENST00000584450.5:c.*268G=	ENSP00000463714.1:n.*268G=
ENST00000584601.5:c.3599G=	ENSP00000462438.1:p.Arg1200=
NM_001005862.2:c.3599G= , LRG_724t1:c.3599G=	NP_001005862.1:p.Arg1200=
NM_001289936.1:c.3644G= , LRG_724t4:c.3644G=	NP_001276865.1:p.Arg1215=
NM_001289937.1:c.*268G=	NP_001276866.1:n.*268G=
NM_004448.3:c.3689G= , LRG_724t2:c.3689G=	NP_004439.2:p.Arg1230=
NR_110535.1:n.4013G=
XM_024450641.1:c.3827G=	XP_024306409.1:p.Arg1276=
XM_024450642.1:c.3782G=	XP_024306410.1:p.Arg1261=
XM_024450643.1:c.3737G=	XP_024306411.1:p.Arg1246=
NM_001005862.3:c.3599G=	NP_001005862.1:p.Arg1200=
NM_001289936.2:c.3644G=	NP_001276865.1:p.Arg1215=
NM_001289937.2:c.*268G=	NP_001276866.1:n.*268G=
NM_001382782.1:c.3599G=	NP_001369711.1:p.Arg1200=
NM_001382783.1:c.3599G=	NP_001369712.1:p.Arg1200=
NM_001382784.1:c.3806G=	NP_001369713.1:p.Arg1269=
NM_001382785.1:c.3791G=	NP_001369714.1:p.Arg1264=
NM_001382786.1:c.3770G=	NP_001369715.1:p.Arg1257=
NM_001382787.1:c.3764G=	NP_001369716.1:p.Arg1255=
NM_001382788.1:c.3719G=	NP_001369717.1:p.Arg1240=
NM_001382789.1:c.3710G=	NP_001369718.1:p.Arg1237=
NM_001382790.1:c.3686G=	NP_001369719.1:p.Arg1229=
NM_001382791.1:c.3680G=	NP_001369720.1:p.Arg1227=
NM_001382792.1:c.3653G=	NP_001369721.1:p.Arg1218=
NM_001382793.1:c.3647G=	NP_001369722.1:p.Arg1216=
NM_001382794.1:c.3647G=	NP_001369723.1:p.Arg1216=
NM_001382795.1:c.3641G=	NP_001369724.1:p.Arg1214=
NM_001382796.1:c.3602G=	NP_001369725.1:p.Arg1201=
NM_001382797.1:c.3590G=	NP_001369726.1:p.Arg1197=
NM_001382798.1:c.3533G=	NP_001369727.1:p.Arg1178=
NM_001382799.1:c.3509G=	NP_001369728.1:p.Arg1170=
NM_001382800.1:c.3503G=	NP_001369729.1:p.Arg1168=
NM_001382801.1:c.3485G=	NP_001369730.1:p.Arg1162=
NM_001382802.1:c.3431G=	NP_001369731.1:p.Arg1144=
NM_001382803.1:c.*268G=	NP_001369732.1:n.*268G=
NM_001382804.1:c.2861G=	NP_001369733.1:p.Arg954=
NM_001382805.1:c.2738G=	NP_001369734.1:p.Arg913=
NM_001382806.1:c.2651G=	NP_001369735.1:p.Arg884=
NM_004448.4:c.3689G= MANE Select	NP_004439.2:p.Arg1230=
NR_110535.2:n.3927G=