Canonical Allele Identifier: CA2259228017

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724821G= , CM000679.2:g.39724821G=	GRCh38
NC_000017.10:g.37881074G= , CM000679.1:g.37881074G=	GRCh37
NC_000017.9:g.35134600G=	NCBI36
NG_007503.1:g.41682G= , LRG_724:g.41682G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2403G= MANE Select	ENSP00000269571.4:p.Met801=
ENST00000269571.9:c.2403G=	ENSP00000269571.4:p.Met801=
ENST00000406381.6:c.2313G=	ENSP00000385185.2:p.Met771=
ENST00000445658.6:c.1575G=	ENSP00000404047.2:p.Met525=
ENST00000541774.5:c.2358G=	ENSP00000446466.1:p.Met786=
ENST00000578373.5:c.*2193G=	ENSP00000463427.1:n.*2193G=
ENST00000580074.1:c.509G=
ENST00000583038.5:n.3537G=
ENST00000584450.5:c.2403G=	ENSP00000463714.1:p.Met801=
ENST00000584601.5:c.2313G=	ENSP00000462438.1:p.Met771=
NM_001005862.2:c.2313G= , LRG_724t1:c.2313G=	NP_001005862.1:p.Met771=
NM_001289936.1:c.2358G= , LRG_724t4:c.2358G=	NP_001276865.1:p.Met786=
NM_001289937.1:c.2403G=	NP_001276866.1:p.Met801=
NM_004448.3:c.2403G= , LRG_724t2:c.2403G=	NP_004439.2:p.Met801=
NR_110535.1:n.2727G=
XM_024450641.1:c.2541G=	XP_024306409.1:p.Met847=
XM_024450642.1:c.2496G=	XP_024306410.1:p.Met832=
XM_024450643.1:c.2451G=	XP_024306411.1:p.Met817=
NM_001005862.3:c.2313G=	NP_001005862.1:p.Met771=
NM_001289936.2:c.2358G=	NP_001276865.1:p.Met786=
NM_001289937.2:c.2403G=	NP_001276866.1:p.Met801=
NM_001382782.1:c.2313G=	NP_001369711.1:p.Met771=
NM_001382783.1:c.2313G=	NP_001369712.1:p.Met771=
NM_001382784.1:c.2520G=	NP_001369713.1:p.Met840=
NM_001382785.1:c.2505G=	NP_001369714.1:p.Met835=
NM_001382786.1:c.2484G=	NP_001369715.1:p.Met828=
NM_001382787.1:c.2478G=	NP_001369716.1:p.Met826=
NM_001382788.1:c.2433G=	NP_001369717.1:p.Met811=
NM_001382789.1:c.2424G=	NP_001369718.1:p.Met808=
NM_001382790.1:c.2400G=	NP_001369719.1:p.Met800=
NM_001382791.1:c.2394G=	NP_001369720.1:p.Met798=
NM_001382792.1:c.2367G=	NP_001369721.1:p.Met789=
NM_001382793.1:c.2361G=	NP_001369722.1:p.Met787=
NM_001382794.1:c.2361G=	NP_001369723.1:p.Met787=
NM_001382795.1:c.2355G=	NP_001369724.1:p.Met785=
NM_001382796.1:c.2403G=	NP_001369725.1:p.Met801=
NM_001382797.1:c.2304G=	NP_001369726.1:p.Met768=
NM_001382798.1:c.2403G=	NP_001369727.1:p.Met801=
NM_001382799.1:c.2223G=	NP_001369728.1:p.Met741=
NM_001382800.1:c.2308-228G=	NP_001369729.1:n.2308-228G=
NM_001382801.1:c.2355G=	NP_001369730.1:p.Met785=
NM_001382802.1:c.2145G=	NP_001369731.1:p.Met715=
NM_001382803.1:c.2361G=	NP_001369732.1:p.Met787=
NM_001382804.1:c.1575G=	NP_001369733.1:p.Met525=
NM_001382805.1:c.2208+1161G=	NP_001369734.1:n.2208+1161G=
NM_001382806.1:c.1365G=	NP_001369735.1:p.Met455=
NM_004448.4:c.2403G= MANE Select	NP_004439.2:p.Met801=
NR_110535.2:n.2641G=