Canonical Allele Identifier: CA2259228787

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727413G= , CM000679.2:g.39727413G=	GRCh38
NC_000017.10:g.37883666G= , CM000679.1:g.37883666G=	GRCh37
NC_000017.9:g.35137192G=	NCBI36
NG_007503.1:g.44274G= , LRG_724:g.44274G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3278G= MANE Select	ENSP00000269571.4:p.Gly1093=
ENST00000269571.9:c.3278G=	ENSP00000269571.4:p.Gly1093=
ENST00000406381.6:c.3188G=	ENSP00000385185.2:p.Gly1063=
ENST00000445658.6:c.2450G=	ENSP00000404047.2:p.Gly817=
ENST00000541774.5:c.3233G=	ENSP00000446466.1:p.Gly1078=
ENST00000578373.5:c.*3068G=	ENSP00000463427.1:n.*3068G=
ENST00000584450.5:c.3160-276G=	ENSP00000463714.1:n.3160-276G=
ENST00000584601.5:c.3188G=	ENSP00000462438.1:p.Gly1063=
NM_001005862.2:c.3188G= , LRG_724t1:c.3188G=	NP_001005862.1:p.Gly1063=
NM_001289936.1:c.3233G= , LRG_724t4:c.3233G=	NP_001276865.1:p.Gly1078=
NM_001289937.1:c.3160-276G=	NP_001276866.1:n.3160-276G=
NM_004448.3:c.3278G= , LRG_724t2:c.3278G=	NP_004439.2:p.Gly1093=
NR_110535.1:n.3602G=
XM_024450641.1:c.3416G=	XP_024306409.1:p.Gly1139=
XM_024450642.1:c.3371G=	XP_024306410.1:p.Gly1124=
XM_024450643.1:c.3326G=	XP_024306411.1:p.Gly1109=
NM_001005862.3:c.3188G=	NP_001005862.1:p.Gly1063=
NM_001289936.2:c.3233G=	NP_001276865.1:p.Gly1078=
NM_001289937.2:c.3160-276G=	NP_001276866.1:n.3160-276G=
NM_001382782.1:c.3188G=	NP_001369711.1:p.Gly1063=
NM_001382783.1:c.3188G=	NP_001369712.1:p.Gly1063=
NM_001382784.1:c.3395G=	NP_001369713.1:p.Gly1132=
NM_001382785.1:c.3380G=	NP_001369714.1:p.Gly1127=
NM_001382786.1:c.3359G=	NP_001369715.1:p.Gly1120=
NM_001382787.1:c.3353G=	NP_001369716.1:p.Gly1118=
NM_001382788.1:c.3308G=	NP_001369717.1:p.Gly1103=
NM_001382789.1:c.3299G=	NP_001369718.1:p.Gly1100=
NM_001382790.1:c.3275G=	NP_001369719.1:p.Gly1092=
NM_001382791.1:c.3269G=	NP_001369720.1:p.Gly1090=
NM_001382792.1:c.3242G=	NP_001369721.1:p.Gly1081=
NM_001382793.1:c.3236G=	NP_001369722.1:p.Gly1079=
NM_001382794.1:c.3236G=	NP_001369723.1:p.Gly1079=
NM_001382795.1:c.3230G=	NP_001369724.1:p.Gly1077=
NM_001382796.1:c.3191G=	NP_001369725.1:p.Gly1064=
NM_001382797.1:c.3179G=	NP_001369726.1:p.Gly1060=
NM_001382798.1:c.3122G=	NP_001369727.1:p.Gly1041=
NM_001382799.1:c.3098G=	NP_001369728.1:p.Gly1033=
NM_001382800.1:c.3092G=	NP_001369729.1:p.Gly1031=
NM_001382801.1:c.3074G=	NP_001369730.1:p.Gly1025=
NM_001382802.1:c.3020G=	NP_001369731.1:p.Gly1007=
NM_001382803.1:c.3118-276G=	NP_001369732.1:n.3118-276G=
NM_001382804.1:c.2450G=	NP_001369733.1:p.Gly817=
NM_001382805.1:c.2327G=	NP_001369734.1:p.Gly776=
NM_001382806.1:c.2240G=	NP_001369735.1:p.Gly747=
NM_004448.4:c.3278G= MANE Select	NP_004439.2:p.Gly1093=
NR_110535.2:n.3516G=