Canonical Allele Identifier: CA2259227999

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724768C= , CM000679.2:g.39724768C=	GRCh38
NC_000017.10:g.37881021C= , CM000679.1:g.37881021C=	GRCh37
NC_000017.9:g.35134547C=	NCBI36
NG_007503.1:g.41629C= , LRG_724:g.41629C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2350C= MANE Select	ENSP00000269571.4:p.Arg784=
ENST00000269571.9:c.2350C=	ENSP00000269571.4:p.Arg784=
ENST00000406381.6:c.2260C=	ENSP00000385185.2:p.Arg754=
ENST00000445658.6:c.1522C=	ENSP00000404047.2:p.Arg508=
ENST00000541774.5:c.2305C=	ENSP00000446466.1:p.Arg769=
ENST00000578373.5:c.*2140C=	ENSP00000463427.1:n.*2140C=
ENST00000580074.1:c.456C=
ENST00000583038.5:n.3484C=
ENST00000584450.5:c.2350C=	ENSP00000463714.1:p.Arg784=
ENST00000584601.5:c.2260C=	ENSP00000462438.1:p.Arg754=
NM_001005862.2:c.2260C= , LRG_724t1:c.2260C=	NP_001005862.1:p.Arg754=
NM_001289936.1:c.2305C= , LRG_724t4:c.2305C=	NP_001276865.1:p.Arg769=
NM_001289937.1:c.2350C=	NP_001276866.1:p.Arg784=
NM_004448.3:c.2350C= , LRG_724t2:c.2350C=	NP_004439.2:p.Arg784=
NR_110535.1:n.2674C=
XM_024450641.1:c.2488C=	XP_024306409.1:p.Arg830=
XM_024450642.1:c.2443C=	XP_024306410.1:p.Arg815=
XM_024450643.1:c.2398C=	XP_024306411.1:p.Arg800=
NM_001005862.3:c.2260C=	NP_001005862.1:p.Arg754=
NM_001289936.2:c.2305C=	NP_001276865.1:p.Arg769=
NM_001289937.2:c.2350C=	NP_001276866.1:p.Arg784=
NM_001382782.1:c.2260C=	NP_001369711.1:p.Arg754=
NM_001382783.1:c.2260C=	NP_001369712.1:p.Arg754=
NM_001382784.1:c.2467C=	NP_001369713.1:p.Arg823=
NM_001382785.1:c.2452C=	NP_001369714.1:p.Arg818=
NM_001382786.1:c.2431C=	NP_001369715.1:p.Arg811=
NM_001382787.1:c.2425C=	NP_001369716.1:p.Arg809=
NM_001382788.1:c.2380C=	NP_001369717.1:p.Arg794=
NM_001382789.1:c.2371C=	NP_001369718.1:p.Arg791=
NM_001382790.1:c.2347C=	NP_001369719.1:p.Arg783=
NM_001382791.1:c.2341C=	NP_001369720.1:p.Arg781=
NM_001382792.1:c.2314C=	NP_001369721.1:p.Arg772=
NM_001382793.1:c.2308C=	NP_001369722.1:p.Arg770=
NM_001382794.1:c.2308C=	NP_001369723.1:p.Arg770=
NM_001382795.1:c.2302C=	NP_001369724.1:p.Arg768=
NM_001382796.1:c.2350C=	NP_001369725.1:p.Arg784=
NM_001382797.1:c.2251C=	NP_001369726.1:p.Arg751=
NM_001382798.1:c.2350C=	NP_001369727.1:p.Arg784=
NM_001382799.1:c.2170C=	NP_001369728.1:p.Arg724=
NM_001382800.1:c.2308-281C=	NP_001369729.1:n.2308-281C=
NM_001382801.1:c.2302C=	NP_001369730.1:p.Arg768=
NM_001382802.1:c.2092C=	NP_001369731.1:p.Arg698=
NM_001382803.1:c.2308C=	NP_001369732.1:p.Arg770=
NM_001382804.1:c.1522C=	NP_001369733.1:p.Arg508=
NM_001382805.1:c.2208+1108C=	NP_001369734.1:n.2208+1108C=
NM_001382806.1:c.1312C=	NP_001369735.1:p.Arg438=
NM_004448.4:c.2350C= MANE Select	NP_004439.2:p.Arg784=
NR_110535.2:n.2588C=