Canonical Allele Identifier: CA2259229257

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727781A= , CM000679.2:g.39727781A=	GRCh38
NC_000017.10:g.37884034A= , CM000679.1:g.37884034A=	GRCh37
NC_000017.9:g.35137560A=	NCBI36
NG_007503.1:g.44642A= , LRG_724:g.44642A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3505A= MANE Select	ENSP00000269571.4:p.Arg1169=
ENST00000269571.9:c.3505A=	ENSP00000269571.4:p.Arg1169=
ENST00000406381.6:c.3415A=	ENSP00000385185.2:p.Arg1139=
ENST00000445658.6:c.2677A=	ENSP00000404047.2:p.Arg893=
ENST00000541774.5:c.3460A=	ENSP00000446466.1:p.Arg1154=
ENST00000578373.5:c.*3295A=	ENSP00000463427.1:n.*3295A=
ENST00000584450.5:c.*84A=	ENSP00000463714.1:n.*84A=
ENST00000584601.5:c.3415A=	ENSP00000462438.1:p.Arg1139=
NM_001005862.2:c.3415A= , LRG_724t1:c.3415A=	NP_001005862.1:p.Arg1139=
NM_001289936.1:c.3460A= , LRG_724t4:c.3460A=	NP_001276865.1:p.Arg1154=
NM_001289937.1:c.*84A=	NP_001276866.1:n.*84A=
NM_004448.3:c.3505A= , LRG_724t2:c.3505A=	NP_004439.2:p.Arg1169=
NR_110535.1:n.3829A=
XM_024450641.1:c.3643A=	XP_024306409.1:p.Arg1215=
XM_024450642.1:c.3598A=	XP_024306410.1:p.Arg1200=
XM_024450643.1:c.3553A=	XP_024306411.1:p.Arg1185=
NM_001005862.3:c.3415A=	NP_001005862.1:p.Arg1139=
NM_001289936.2:c.3460A=	NP_001276865.1:p.Arg1154=
NM_001289937.2:c.*84A=	NP_001276866.1:n.*84A=
NM_001382782.1:c.3415A=	NP_001369711.1:p.Arg1139=
NM_001382783.1:c.3415A=	NP_001369712.1:p.Arg1139=
NM_001382784.1:c.3622A=	NP_001369713.1:p.Arg1208=
NM_001382785.1:c.3607A=	NP_001369714.1:p.Arg1203=
NM_001382786.1:c.3586A=	NP_001369715.1:p.Arg1196=
NM_001382787.1:c.3580A=	NP_001369716.1:p.Arg1194=
NM_001382788.1:c.3535A=	NP_001369717.1:p.Arg1179=
NM_001382789.1:c.3526A=	NP_001369718.1:p.Arg1176=
NM_001382790.1:c.3502A=	NP_001369719.1:p.Arg1168=
NM_001382791.1:c.3496A=	NP_001369720.1:p.Arg1166=
NM_001382792.1:c.3469A=	NP_001369721.1:p.Arg1157=
NM_001382793.1:c.3463A=	NP_001369722.1:p.Arg1155=
NM_001382794.1:c.3463A=	NP_001369723.1:p.Arg1155=
NM_001382795.1:c.3457A=	NP_001369724.1:p.Arg1153=
NM_001382796.1:c.3418A=	NP_001369725.1:p.Arg1140=
NM_001382797.1:c.3406A=	NP_001369726.1:p.Arg1136=
NM_001382798.1:c.3349A=	NP_001369727.1:p.Arg1117=
NM_001382799.1:c.3325A=	NP_001369728.1:p.Arg1109=
NM_001382800.1:c.3319A=	NP_001369729.1:p.Arg1107=
NM_001382801.1:c.3301A=	NP_001369730.1:p.Arg1101=
NM_001382802.1:c.3247A=	NP_001369731.1:p.Arg1083=
NM_001382803.1:c.*84A=	NP_001369732.1:n.*84A=
NM_001382804.1:c.2677A=	NP_001369733.1:p.Arg893=
NM_001382805.1:c.2554A=	NP_001369734.1:p.Arg852=
NM_001382806.1:c.2467A=	NP_001369735.1:p.Arg823=
NM_004448.4:c.3505A= MANE Select	NP_004439.2:p.Arg1169=
NR_110535.2:n.3743A=