Canonical Allele Identifier: CA2259228700

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727350G= , CM000679.2:g.39727350G=	GRCh38
NC_000017.10:g.37883603G= , CM000679.1:g.37883603G=	GRCh37
NC_000017.9:g.35137129G=	NCBI36
NG_007503.1:g.44211G= , LRG_724:g.44211G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3215G= MANE Select	ENSP00000269571.4:p.Arg1072=
ENST00000269571.9:c.3215G=	ENSP00000269571.4:p.Arg1072=
ENST00000406381.6:c.3125G=	ENSP00000385185.2:p.Arg1042=
ENST00000445658.6:c.2387G=	ENSP00000404047.2:p.Arg796=
ENST00000541774.5:c.3170G=	ENSP00000446466.1:p.Arg1057=
ENST00000578373.5:c.*3005G=	ENSP00000463427.1:n.*3005G=
ENST00000584450.5:c.3160-339G=	ENSP00000463714.1:n.3160-339G=
ENST00000584601.5:c.3125G=	ENSP00000462438.1:p.Arg1042=
NM_001005862.2:c.3125G= , LRG_724t1:c.3125G=	NP_001005862.1:p.Arg1042=
NM_001289936.1:c.3170G= , LRG_724t4:c.3170G=	NP_001276865.1:p.Arg1057=
NM_001289937.1:c.3160-339G=	NP_001276866.1:n.3160-339G=
NM_004448.3:c.3215G= , LRG_724t2:c.3215G=	NP_004439.2:p.Arg1072=
NR_110535.1:n.3539G=
XM_024450641.1:c.3353G=	XP_024306409.1:p.Arg1118=
XM_024450642.1:c.3308G=	XP_024306410.1:p.Arg1103=
XM_024450643.1:c.3263G=	XP_024306411.1:p.Arg1088=
NM_001005862.3:c.3125G=	NP_001005862.1:p.Arg1042=
NM_001289936.2:c.3170G=	NP_001276865.1:p.Arg1057=
NM_001289937.2:c.3160-339G=	NP_001276866.1:n.3160-339G=
NM_001382782.1:c.3125G=	NP_001369711.1:p.Arg1042=
NM_001382783.1:c.3125G=	NP_001369712.1:p.Arg1042=
NM_001382784.1:c.3332G=	NP_001369713.1:p.Arg1111=
NM_001382785.1:c.3317G=	NP_001369714.1:p.Arg1106=
NM_001382786.1:c.3296G=	NP_001369715.1:p.Arg1099=
NM_001382787.1:c.3290G=	NP_001369716.1:p.Arg1097=
NM_001382788.1:c.3245G=	NP_001369717.1:p.Arg1082=
NM_001382789.1:c.3236G=	NP_001369718.1:p.Arg1079=
NM_001382790.1:c.3212G=	NP_001369719.1:p.Arg1071=
NM_001382791.1:c.3206G=	NP_001369720.1:p.Arg1069=
NM_001382792.1:c.3179G=	NP_001369721.1:p.Arg1060=
NM_001382793.1:c.3173G=	NP_001369722.1:p.Arg1058=
NM_001382794.1:c.3173G=	NP_001369723.1:p.Arg1058=
NM_001382795.1:c.3167G=	NP_001369724.1:p.Arg1056=
NM_001382796.1:c.3128G=	NP_001369725.1:p.Arg1043=
NM_001382797.1:c.3116G=	NP_001369726.1:p.Arg1039=
NM_001382798.1:c.3059G=	NP_001369727.1:p.Arg1020=
NM_001382799.1:c.3035G=	NP_001369728.1:p.Arg1012=
NM_001382800.1:c.3029G=	NP_001369729.1:p.Arg1010=
NM_001382801.1:c.3011G=	NP_001369730.1:p.Arg1004=
NM_001382802.1:c.2957G=	NP_001369731.1:p.Arg986=
NM_001382803.1:c.3118-339G=	NP_001369732.1:n.3118-339G=
NM_001382804.1:c.2387G=	NP_001369733.1:p.Arg796=
NM_001382805.1:c.2264G=	NP_001369734.1:p.Arg755=
NM_001382806.1:c.2177G=	NP_001369735.1:p.Arg726=
NM_004448.4:c.3215G= MANE Select	NP_004439.2:p.Arg1072=
NR_110535.2:n.3453G=