Canonical Allele Identifier: CA2259229241

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727741C= , CM000679.2:g.39727741C=	GRCh38
NC_000017.10:g.37883994C= , CM000679.1:g.37883994C=	GRCh37
NC_000017.9:g.35137520C=	NCBI36
NG_007503.1:g.44602C= , LRG_724:g.44602C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3465C= MANE Select	ENSP00000269571.4:p.Gly1155=
ENST00000269571.9:c.3465C=	ENSP00000269571.4:p.Gly1155=
ENST00000406381.6:c.3375C=	ENSP00000385185.2:p.Gly1125=
ENST00000445658.6:c.2637C=	ENSP00000404047.2:p.Gly879=
ENST00000541774.5:c.3420C=	ENSP00000446466.1:p.Gly1140=
ENST00000578373.5:c.*3255C=	ENSP00000463427.1:n.*3255C=
ENST00000584450.5:c.*44C=	ENSP00000463714.1:n.*44C=
ENST00000584601.5:c.3375C=	ENSP00000462438.1:p.Gly1125=
NM_001005862.2:c.3375C= , LRG_724t1:c.3375C=	NP_001005862.1:p.Gly1125=
NM_001289936.1:c.3420C= , LRG_724t4:c.3420C=	NP_001276865.1:p.Gly1140=
NM_001289937.1:c.*44C=	NP_001276866.1:n.*44C=
NM_004448.3:c.3465C= , LRG_724t2:c.3465C=	NP_004439.2:p.Gly1155=
NR_110535.1:n.3789C=
XM_024450641.1:c.3603C=	XP_024306409.1:p.Gly1201=
XM_024450642.1:c.3558C=	XP_024306410.1:p.Gly1186=
XM_024450643.1:c.3513C=	XP_024306411.1:p.Gly1171=
NM_001005862.3:c.3375C=	NP_001005862.1:p.Gly1125=
NM_001289936.2:c.3420C=	NP_001276865.1:p.Gly1140=
NM_001289937.2:c.*44C=	NP_001276866.1:n.*44C=
NM_001382782.1:c.3375C=	NP_001369711.1:p.Gly1125=
NM_001382783.1:c.3375C=	NP_001369712.1:p.Gly1125=
NM_001382784.1:c.3582C=	NP_001369713.1:p.Gly1194=
NM_001382785.1:c.3567C=	NP_001369714.1:p.Gly1189=
NM_001382786.1:c.3546C=	NP_001369715.1:p.Gly1182=
NM_001382787.1:c.3540C=	NP_001369716.1:p.Gly1180=
NM_001382788.1:c.3495C=	NP_001369717.1:p.Gly1165=
NM_001382789.1:c.3486C=	NP_001369718.1:p.Gly1162=
NM_001382790.1:c.3462C=	NP_001369719.1:p.Gly1154=
NM_001382791.1:c.3456C=	NP_001369720.1:p.Gly1152=
NM_001382792.1:c.3429C=	NP_001369721.1:p.Gly1143=
NM_001382793.1:c.3423C=	NP_001369722.1:p.Gly1141=
NM_001382794.1:c.3423C=	NP_001369723.1:p.Gly1141=
NM_001382795.1:c.3417C=	NP_001369724.1:p.Gly1139=
NM_001382796.1:c.3378C=	NP_001369725.1:p.Gly1126=
NM_001382797.1:c.3366C=	NP_001369726.1:p.Gly1122=
NM_001382798.1:c.3309C=	NP_001369727.1:p.Gly1103=
NM_001382799.1:c.3285C=	NP_001369728.1:p.Gly1095=
NM_001382800.1:c.3279C=	NP_001369729.1:p.Gly1093=
NM_001382801.1:c.3261C=	NP_001369730.1:p.Gly1087=
NM_001382802.1:c.3207C=	NP_001369731.1:p.Gly1069=
NM_001382803.1:c.*44C=	NP_001369732.1:n.*44C=
NM_001382804.1:c.2637C=	NP_001369733.1:p.Gly879=
NM_001382805.1:c.2514C=	NP_001369734.1:p.Gly838=
NM_001382806.1:c.2427C=	NP_001369735.1:p.Gly809=
NM_004448.4:c.3465C= MANE Select	NP_004439.2:p.Gly1155=
NR_110535.2:n.3703C=