Canonical Allele Identifier: CA2259229318

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727924C= , CM000679.2:g.39727924C=	GRCh38
NC_000017.10:g.37884177C= , CM000679.1:g.37884177C=	GRCh37
NC_000017.9:g.35137703C=	NCBI36
NG_007503.1:g.44785C= , LRG_724:g.44785C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3648C= MANE Select	ENSP00000269571.4:p.Ala1216=
ENST00000269571.9:c.3648C=	ENSP00000269571.4:p.Ala1216=
ENST00000406381.6:c.3558C=	ENSP00000385185.2:p.Ala1186=
ENST00000445658.6:c.2820C=	ENSP00000404047.2:p.Ala940=
ENST00000541774.5:c.3603C=	ENSP00000446466.1:p.Ala1201=
ENST00000578373.5:c.*3438C=	ENSP00000463427.1:n.*3438C=
ENST00000584450.5:c.*227C=	ENSP00000463714.1:n.*227C=
ENST00000584601.5:c.3558C=	ENSP00000462438.1:p.Ala1186=
NM_001005862.2:c.3558C= , LRG_724t1:c.3558C=	NP_001005862.1:p.Ala1186=
NM_001289936.1:c.3603C= , LRG_724t4:c.3603C=	NP_001276865.1:p.Ala1201=
NM_001289937.1:c.*227C=	NP_001276866.1:n.*227C=
NM_004448.3:c.3648C= , LRG_724t2:c.3648C=	NP_004439.2:p.Ala1216=
NR_110535.1:n.3972C=
XM_024450641.1:c.3786C=	XP_024306409.1:p.Ala1262=
XM_024450642.1:c.3741C=	XP_024306410.1:p.Ala1247=
XM_024450643.1:c.3696C=	XP_024306411.1:p.Ala1232=
NM_001005862.3:c.3558C=	NP_001005862.1:p.Ala1186=
NM_001289936.2:c.3603C=	NP_001276865.1:p.Ala1201=
NM_001289937.2:c.*227C=	NP_001276866.1:n.*227C=
NM_001382782.1:c.3558C=	NP_001369711.1:p.Ala1186=
NM_001382783.1:c.3558C=	NP_001369712.1:p.Ala1186=
NM_001382784.1:c.3765C=	NP_001369713.1:p.Ala1255=
NM_001382785.1:c.3750C=	NP_001369714.1:p.Ala1250=
NM_001382786.1:c.3729C=	NP_001369715.1:p.Ala1243=
NM_001382787.1:c.3723C=	NP_001369716.1:p.Ala1241=
NM_001382788.1:c.3678C=	NP_001369717.1:p.Ala1226=
NM_001382789.1:c.3669C=	NP_001369718.1:p.Ala1223=
NM_001382790.1:c.3645C=	NP_001369719.1:p.Ala1215=
NM_001382791.1:c.3639C=	NP_001369720.1:p.Ala1213=
NM_001382792.1:c.3612C=	NP_001369721.1:p.Ala1204=
NM_001382793.1:c.3606C=	NP_001369722.1:p.Ala1202=
NM_001382794.1:c.3606C=	NP_001369723.1:p.Ala1202=
NM_001382795.1:c.3600C=	NP_001369724.1:p.Ala1200=
NM_001382796.1:c.3561C=	NP_001369725.1:p.Ala1187=
NM_001382797.1:c.3549C=	NP_001369726.1:p.Ala1183=
NM_001382798.1:c.3492C=	NP_001369727.1:p.Ala1164=
NM_001382799.1:c.3468C=	NP_001369728.1:p.Ala1156=
NM_001382800.1:c.3462C=	NP_001369729.1:p.Ala1154=
NM_001382801.1:c.3444C=	NP_001369730.1:p.Ala1148=
NM_001382802.1:c.3390C=	NP_001369731.1:p.Ala1130=
NM_001382803.1:c.*227C=	NP_001369732.1:n.*227C=
NM_001382804.1:c.2820C=	NP_001369733.1:p.Ala940=
NM_001382805.1:c.2697C=	NP_001369734.1:p.Ala899=
NM_001382806.1:c.2610C=	NP_001369735.1:p.Ala870=
NM_004448.4:c.3648C= MANE Select	NP_004439.2:p.Ala1216=
NR_110535.2:n.3886C=