Canonical Allele Identifier: CA2259229276

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727817G= , CM000679.2:g.39727817G=	GRCh38
NC_000017.10:g.37884070G= , CM000679.1:g.37884070G=	GRCh37
NC_000017.9:g.35137596G=	NCBI36
NG_007503.1:g.44678G= , LRG_724:g.44678G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3541G= MANE Select	ENSP00000269571.4:p.Val1181=
ENST00000269571.9:c.3541G=	ENSP00000269571.4:p.Val1181=
ENST00000406381.6:c.3451G=	ENSP00000385185.2:p.Val1151=
ENST00000445658.6:c.2713G=	ENSP00000404047.2:p.Val905=
ENST00000541774.5:c.3496G=	ENSP00000446466.1:p.Val1166=
ENST00000578373.5:c.*3331G=	ENSP00000463427.1:n.*3331G=
ENST00000584450.5:c.*120G=	ENSP00000463714.1:n.*120G=
ENST00000584601.5:c.3451G=	ENSP00000462438.1:p.Val1151=
NM_001005862.2:c.3451G= , LRG_724t1:c.3451G=	NP_001005862.1:p.Val1151=
NM_001289936.1:c.3496G= , LRG_724t4:c.3496G=	NP_001276865.1:p.Val1166=
NM_001289937.1:c.*120G=	NP_001276866.1:n.*120G=
NM_004448.3:c.3541G= , LRG_724t2:c.3541G=	NP_004439.2:p.Val1181=
NR_110535.1:n.3865G=
XM_024450641.1:c.3679G=	XP_024306409.1:p.Val1227=
XM_024450642.1:c.3634G=	XP_024306410.1:p.Val1212=
XM_024450643.1:c.3589G=	XP_024306411.1:p.Val1197=
NM_001005862.3:c.3451G=	NP_001005862.1:p.Val1151=
NM_001289936.2:c.3496G=	NP_001276865.1:p.Val1166=
NM_001289937.2:c.*120G=	NP_001276866.1:n.*120G=
NM_001382782.1:c.3451G=	NP_001369711.1:p.Val1151=
NM_001382783.1:c.3451G=	NP_001369712.1:p.Val1151=
NM_001382784.1:c.3658G=	NP_001369713.1:p.Val1220=
NM_001382785.1:c.3643G=	NP_001369714.1:p.Val1215=
NM_001382786.1:c.3622G=	NP_001369715.1:p.Val1208=
NM_001382787.1:c.3616G=	NP_001369716.1:p.Val1206=
NM_001382788.1:c.3571G=	NP_001369717.1:p.Val1191=
NM_001382789.1:c.3562G=	NP_001369718.1:p.Val1188=
NM_001382790.1:c.3538G=	NP_001369719.1:p.Val1180=
NM_001382791.1:c.3532G=	NP_001369720.1:p.Val1178=
NM_001382792.1:c.3505G=	NP_001369721.1:p.Val1169=
NM_001382793.1:c.3499G=	NP_001369722.1:p.Val1167=
NM_001382794.1:c.3499G=	NP_001369723.1:p.Val1167=
NM_001382795.1:c.3493G=	NP_001369724.1:p.Val1165=
NM_001382796.1:c.3454G=	NP_001369725.1:p.Val1152=
NM_001382797.1:c.3442G=	NP_001369726.1:p.Val1148=
NM_001382798.1:c.3385G=	NP_001369727.1:p.Val1129=
NM_001382799.1:c.3361G=	NP_001369728.1:p.Val1121=
NM_001382800.1:c.3355G=	NP_001369729.1:p.Val1119=
NM_001382801.1:c.3337G=	NP_001369730.1:p.Val1113=
NM_001382802.1:c.3283G=	NP_001369731.1:p.Val1095=
NM_001382803.1:c.*120G=	NP_001369732.1:n.*120G=
NM_001382804.1:c.2713G=	NP_001369733.1:p.Val905=
NM_001382805.1:c.2590G=	NP_001369734.1:p.Val864=
NM_001382806.1:c.2503G=	NP_001369735.1:p.Val835=
NM_004448.4:c.3541G= MANE Select	NP_004439.2:p.Val1181=
NR_110535.2:n.3779G=