Canonical Allele Identifier: CA2259229316

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727915C= , CM000679.2:g.39727915C=	GRCh38
NC_000017.10:g.37884168C= , CM000679.1:g.37884168C=	GRCh37
NC_000017.9:g.35137694C=	NCBI36
NG_007503.1:g.44776C= , LRG_724:g.44776C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3639C= MANE Select	ENSP00000269571.4:p.Phe1213=
ENST00000269571.9:c.3639C=	ENSP00000269571.4:p.Phe1213=
ENST00000406381.6:c.3549C=	ENSP00000385185.2:p.Phe1183=
ENST00000445658.6:c.2811C=	ENSP00000404047.2:p.Phe937=
ENST00000541774.5:c.3594C=	ENSP00000446466.1:p.Phe1198=
ENST00000578373.5:c.*3429C=	ENSP00000463427.1:n.*3429C=
ENST00000584450.5:c.*218C=	ENSP00000463714.1:n.*218C=
ENST00000584601.5:c.3549C=	ENSP00000462438.1:p.Phe1183=
NM_001005862.2:c.3549C= , LRG_724t1:c.3549C=	NP_001005862.1:p.Phe1183=
NM_001289936.1:c.3594C= , LRG_724t4:c.3594C=	NP_001276865.1:p.Phe1198=
NM_001289937.1:c.*218C=	NP_001276866.1:n.*218C=
NM_004448.3:c.3639C= , LRG_724t2:c.3639C=	NP_004439.2:p.Phe1213=
NR_110535.1:n.3963C=
XM_024450641.1:c.3777C=	XP_024306409.1:p.Phe1259=
XM_024450642.1:c.3732C=	XP_024306410.1:p.Phe1244=
XM_024450643.1:c.3687C=	XP_024306411.1:p.Phe1229=
NM_001005862.3:c.3549C=	NP_001005862.1:p.Phe1183=
NM_001289936.2:c.3594C=	NP_001276865.1:p.Phe1198=
NM_001289937.2:c.*218C=	NP_001276866.1:n.*218C=
NM_001382782.1:c.3549C=	NP_001369711.1:p.Phe1183=
NM_001382783.1:c.3549C=	NP_001369712.1:p.Phe1183=
NM_001382784.1:c.3756C=	NP_001369713.1:p.Phe1252=
NM_001382785.1:c.3741C=	NP_001369714.1:p.Phe1247=
NM_001382786.1:c.3720C=	NP_001369715.1:p.Phe1240=
NM_001382787.1:c.3714C=	NP_001369716.1:p.Phe1238=
NM_001382788.1:c.3669C=	NP_001369717.1:p.Phe1223=
NM_001382789.1:c.3660C=	NP_001369718.1:p.Phe1220=
NM_001382790.1:c.3636C=	NP_001369719.1:p.Phe1212=
NM_001382791.1:c.3630C=	NP_001369720.1:p.Phe1210=
NM_001382792.1:c.3603C=	NP_001369721.1:p.Phe1201=
NM_001382793.1:c.3597C=	NP_001369722.1:p.Phe1199=
NM_001382794.1:c.3597C=	NP_001369723.1:p.Phe1199=
NM_001382795.1:c.3591C=	NP_001369724.1:p.Phe1197=
NM_001382796.1:c.3552C=	NP_001369725.1:p.Phe1184=
NM_001382797.1:c.3540C=	NP_001369726.1:p.Phe1180=
NM_001382798.1:c.3483C=	NP_001369727.1:p.Phe1161=
NM_001382799.1:c.3459C=	NP_001369728.1:p.Phe1153=
NM_001382800.1:c.3453C=	NP_001369729.1:p.Phe1151=
NM_001382801.1:c.3435C=	NP_001369730.1:p.Phe1145=
NM_001382802.1:c.3381C=	NP_001369731.1:p.Phe1127=
NM_001382803.1:c.*218C=	NP_001369732.1:n.*218C=
NM_001382804.1:c.2811C=	NP_001369733.1:p.Phe937=
NM_001382805.1:c.2688C=	NP_001369734.1:p.Phe896=
NM_001382806.1:c.2601C=	NP_001369735.1:p.Phe867=
NM_004448.4:c.3639C= MANE Select	NP_004439.2:p.Phe1213=
NR_110535.2:n.3877C=