Canonical Allele Identifier: CA2259228762

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727394G= , CM000679.2:g.39727394G=	GRCh38
NC_000017.10:g.37883647G= , CM000679.1:g.37883647G=	GRCh37
NC_000017.9:g.35137173G=	NCBI36
NG_007503.1:g.44255G= , LRG_724:g.44255G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3259G= MANE Select	ENSP00000269571.4:p.Asp1087=
ENST00000269571.9:c.3259G=	ENSP00000269571.4:p.Asp1087=
ENST00000406381.6:c.3169G=	ENSP00000385185.2:p.Asp1057=
ENST00000445658.6:c.2431G=	ENSP00000404047.2:p.Asp811=
ENST00000541774.5:c.3214G=	ENSP00000446466.1:p.Asp1072=
ENST00000578373.5:c.*3049G=	ENSP00000463427.1:n.*3049G=
ENST00000584450.5:c.3160-295G=	ENSP00000463714.1:n.3160-295G=
ENST00000584601.5:c.3169G=	ENSP00000462438.1:p.Asp1057=
NM_001005862.2:c.3169G= , LRG_724t1:c.3169G=	NP_001005862.1:p.Asp1057=
NM_001289936.1:c.3214G= , LRG_724t4:c.3214G=	NP_001276865.1:p.Asp1072=
NM_001289937.1:c.3160-295G=	NP_001276866.1:n.3160-295G=
NM_004448.3:c.3259G= , LRG_724t2:c.3259G=	NP_004439.2:p.Asp1087=
NR_110535.1:n.3583G=
XM_024450641.1:c.3397G=	XP_024306409.1:p.Asp1133=
XM_024450642.1:c.3352G=	XP_024306410.1:p.Asp1118=
XM_024450643.1:c.3307G=	XP_024306411.1:p.Asp1103=
NM_001005862.3:c.3169G=	NP_001005862.1:p.Asp1057=
NM_001289936.2:c.3214G=	NP_001276865.1:p.Asp1072=
NM_001289937.2:c.3160-295G=	NP_001276866.1:n.3160-295G=
NM_001382782.1:c.3169G=	NP_001369711.1:p.Asp1057=
NM_001382783.1:c.3169G=	NP_001369712.1:p.Asp1057=
NM_001382784.1:c.3376G=	NP_001369713.1:p.Asp1126=
NM_001382785.1:c.3361G=	NP_001369714.1:p.Asp1121=
NM_001382786.1:c.3340G=	NP_001369715.1:p.Asp1114=
NM_001382787.1:c.3334G=	NP_001369716.1:p.Asp1112=
NM_001382788.1:c.3289G=	NP_001369717.1:p.Asp1097=
NM_001382789.1:c.3280G=	NP_001369718.1:p.Asp1094=
NM_001382790.1:c.3256G=	NP_001369719.1:p.Asp1086=
NM_001382791.1:c.3250G=	NP_001369720.1:p.Asp1084=
NM_001382792.1:c.3223G=	NP_001369721.1:p.Asp1075=
NM_001382793.1:c.3217G=	NP_001369722.1:p.Asp1073=
NM_001382794.1:c.3217G=	NP_001369723.1:p.Asp1073=
NM_001382795.1:c.3211G=	NP_001369724.1:p.Asp1071=
NM_001382796.1:c.3172G=	NP_001369725.1:p.Asp1058=
NM_001382797.1:c.3160G=	NP_001369726.1:p.Asp1054=
NM_001382798.1:c.3103G=	NP_001369727.1:p.Asp1035=
NM_001382799.1:c.3079G=	NP_001369728.1:p.Asp1027=
NM_001382800.1:c.3073G=	NP_001369729.1:p.Asp1025=
NM_001382801.1:c.3055G=	NP_001369730.1:p.Asp1019=
NM_001382802.1:c.3001G=	NP_001369731.1:p.Asp1001=
NM_001382803.1:c.3118-295G=	NP_001369732.1:n.3118-295G=
NM_001382804.1:c.2431G=	NP_001369733.1:p.Asp811=
NM_001382805.1:c.2308G=	NP_001369734.1:p.Asp770=
NM_001382806.1:c.2221G=	NP_001369735.1:p.Asp741=
NM_004448.4:c.3259G= MANE Select	NP_004439.2:p.Asp1087=
NR_110535.2:n.3497G=