Canonical Allele Identifier: CA2259229320

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727927C= , CM000679.2:g.39727927C=	GRCh38
NC_000017.10:g.37884180C= , CM000679.1:g.37884180C=	GRCh37
NC_000017.9:g.35137706C=	NCBI36
NG_007503.1:g.44788C= , LRG_724:g.44788C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3651C= MANE Select	ENSP00000269571.4:p.Phe1217=
ENST00000269571.9:c.3651C=	ENSP00000269571.4:p.Phe1217=
ENST00000406381.6:c.3561C=	ENSP00000385185.2:p.Phe1187=
ENST00000445658.6:c.2823C=	ENSP00000404047.2:p.Phe941=
ENST00000541774.5:c.3606C=	ENSP00000446466.1:p.Phe1202=
ENST00000578373.5:c.*3441C=	ENSP00000463427.1:n.*3441C=
ENST00000584450.5:c.*230C=	ENSP00000463714.1:n.*230C=
ENST00000584601.5:c.3561C=	ENSP00000462438.1:p.Phe1187=
NM_001005862.2:c.3561C= , LRG_724t1:c.3561C=	NP_001005862.1:p.Phe1187=
NM_001289936.1:c.3606C= , LRG_724t4:c.3606C=	NP_001276865.1:p.Phe1202=
NM_001289937.1:c.*230C=	NP_001276866.1:n.*230C=
NM_004448.3:c.3651C= , LRG_724t2:c.3651C=	NP_004439.2:p.Phe1217=
NR_110535.1:n.3975C=
XM_024450641.1:c.3789C=	XP_024306409.1:p.Phe1263=
XM_024450642.1:c.3744C=	XP_024306410.1:p.Phe1248=
XM_024450643.1:c.3699C=	XP_024306411.1:p.Phe1233=
NM_001005862.3:c.3561C=	NP_001005862.1:p.Phe1187=
NM_001289936.2:c.3606C=	NP_001276865.1:p.Phe1202=
NM_001289937.2:c.*230C=	NP_001276866.1:n.*230C=
NM_001382782.1:c.3561C=	NP_001369711.1:p.Phe1187=
NM_001382783.1:c.3561C=	NP_001369712.1:p.Phe1187=
NM_001382784.1:c.3768C=	NP_001369713.1:p.Phe1256=
NM_001382785.1:c.3753C=	NP_001369714.1:p.Phe1251=
NM_001382786.1:c.3732C=	NP_001369715.1:p.Phe1244=
NM_001382787.1:c.3726C=	NP_001369716.1:p.Phe1242=
NM_001382788.1:c.3681C=	NP_001369717.1:p.Phe1227=
NM_001382789.1:c.3672C=	NP_001369718.1:p.Phe1224=
NM_001382790.1:c.3648C=	NP_001369719.1:p.Phe1216=
NM_001382791.1:c.3642C=	NP_001369720.1:p.Phe1214=
NM_001382792.1:c.3615C=	NP_001369721.1:p.Phe1205=
NM_001382793.1:c.3609C=	NP_001369722.1:p.Phe1203=
NM_001382794.1:c.3609C=	NP_001369723.1:p.Phe1203=
NM_001382795.1:c.3603C=	NP_001369724.1:p.Phe1201=
NM_001382796.1:c.3564C=	NP_001369725.1:p.Phe1188=
NM_001382797.1:c.3552C=	NP_001369726.1:p.Phe1184=
NM_001382798.1:c.3495C=	NP_001369727.1:p.Phe1165=
NM_001382799.1:c.3471C=	NP_001369728.1:p.Phe1157=
NM_001382800.1:c.3465C=	NP_001369729.1:p.Phe1155=
NM_001382801.1:c.3447C=	NP_001369730.1:p.Phe1149=
NM_001382802.1:c.3393C=	NP_001369731.1:p.Phe1131=
NM_001382803.1:c.*230C=	NP_001369732.1:n.*230C=
NM_001382804.1:c.2823C=	NP_001369733.1:p.Phe941=
NM_001382805.1:c.2700C=	NP_001369734.1:p.Phe900=
NM_001382806.1:c.2613C=	NP_001369735.1:p.Phe871=
NM_004448.4:c.3651C= MANE Select	NP_004439.2:p.Phe1217=
NR_110535.2:n.3889C=