Canonical Allele Identifier: CA2259229332

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727956C= , CM000679.2:g.39727956C=	GRCh38
NC_000017.10:g.37884209C= , CM000679.1:g.37884209C=	GRCh37
NC_000017.9:g.35137735C=	NCBI36
NG_007503.1:g.44817C= , LRG_724:g.44817C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3680C= MANE Select	ENSP00000269571.4:p.Pro1227=
ENST00000269571.9:c.3680C=	ENSP00000269571.4:p.Pro1227=
ENST00000406381.6:c.3590C=	ENSP00000385185.2:p.Pro1197=
ENST00000445658.6:c.2852C=	ENSP00000404047.2:p.Pro951=
ENST00000541774.5:c.3635C=	ENSP00000446466.1:p.Pro1212=
ENST00000578373.5:c.*3470C=	ENSP00000463427.1:n.*3470C=
ENST00000584450.5:c.*259C=	ENSP00000463714.1:n.*259C=
ENST00000584601.5:c.3590C=	ENSP00000462438.1:p.Pro1197=
NM_001005862.2:c.3590C= , LRG_724t1:c.3590C=	NP_001005862.1:p.Pro1197=
NM_001289936.1:c.3635C= , LRG_724t4:c.3635C=	NP_001276865.1:p.Pro1212=
NM_001289937.1:c.*259C=	NP_001276866.1:n.*259C=
NM_004448.3:c.3680C= , LRG_724t2:c.3680C=	NP_004439.2:p.Pro1227=
NR_110535.1:n.4004C=
XM_024450641.1:c.3818C=	XP_024306409.1:p.Pro1273=
XM_024450642.1:c.3773C=	XP_024306410.1:p.Pro1258=
XM_024450643.1:c.3728C=	XP_024306411.1:p.Pro1243=
NM_001005862.3:c.3590C=	NP_001005862.1:p.Pro1197=
NM_001289936.2:c.3635C=	NP_001276865.1:p.Pro1212=
NM_001289937.2:c.*259C=	NP_001276866.1:n.*259C=
NM_001382782.1:c.3590C=	NP_001369711.1:p.Pro1197=
NM_001382783.1:c.3590C=	NP_001369712.1:p.Pro1197=
NM_001382784.1:c.3797C=	NP_001369713.1:p.Pro1266=
NM_001382785.1:c.3782C=	NP_001369714.1:p.Pro1261=
NM_001382786.1:c.3761C=	NP_001369715.1:p.Pro1254=
NM_001382787.1:c.3755C=	NP_001369716.1:p.Pro1252=
NM_001382788.1:c.3710C=	NP_001369717.1:p.Pro1237=
NM_001382789.1:c.3701C=	NP_001369718.1:p.Pro1234=
NM_001382790.1:c.3677C=	NP_001369719.1:p.Pro1226=
NM_001382791.1:c.3671C=	NP_001369720.1:p.Pro1224=
NM_001382792.1:c.3644C=	NP_001369721.1:p.Pro1215=
NM_001382793.1:c.3638C=	NP_001369722.1:p.Pro1213=
NM_001382794.1:c.3638C=	NP_001369723.1:p.Pro1213=
NM_001382795.1:c.3632C=	NP_001369724.1:p.Pro1211=
NM_001382796.1:c.3593C=	NP_001369725.1:p.Pro1198=
NM_001382797.1:c.3581C=	NP_001369726.1:p.Pro1194=
NM_001382798.1:c.3524C=	NP_001369727.1:p.Pro1175=
NM_001382799.1:c.3500C=	NP_001369728.1:p.Pro1167=
NM_001382800.1:c.3494C=	NP_001369729.1:p.Pro1165=
NM_001382801.1:c.3476C=	NP_001369730.1:p.Pro1159=
NM_001382802.1:c.3422C=	NP_001369731.1:p.Pro1141=
NM_001382803.1:c.*259C=	NP_001369732.1:n.*259C=
NM_001382804.1:c.2852C=	NP_001369733.1:p.Pro951=
NM_001382805.1:c.2729C=	NP_001369734.1:p.Pro910=
NM_001382806.1:c.2642C=	NP_001369735.1:p.Pro881=
NM_004448.4:c.3680C= MANE Select	NP_004439.2:p.Pro1227=
NR_110535.2:n.3918C=