Canonical Allele Identifier: CA2259229319

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727925T= , CM000679.2:g.39727925T=	GRCh38
NC_000017.10:g.37884178T= , CM000679.1:g.37884178T=	GRCh37
NC_000017.9:g.35137704T=	NCBI36
NG_007503.1:g.44786T= , LRG_724:g.44786T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3649T= MANE Select	ENSP00000269571.4:p.Phe1217=
ENST00000269571.9:c.3649T=	ENSP00000269571.4:p.Phe1217=
ENST00000406381.6:c.3559T=	ENSP00000385185.2:p.Phe1187=
ENST00000445658.6:c.2821T=	ENSP00000404047.2:p.Phe941=
ENST00000541774.5:c.3604T=	ENSP00000446466.1:p.Phe1202=
ENST00000578373.5:c.*3439T=	ENSP00000463427.1:n.*3439T=
ENST00000584450.5:c.*228T=	ENSP00000463714.1:n.*228T=
ENST00000584601.5:c.3559T=	ENSP00000462438.1:p.Phe1187=
NM_001005862.2:c.3559T= , LRG_724t1:c.3559T=	NP_001005862.1:p.Phe1187=
NM_001289936.1:c.3604T= , LRG_724t4:c.3604T=	NP_001276865.1:p.Phe1202=
NM_001289937.1:c.*228T=	NP_001276866.1:n.*228T=
NM_004448.3:c.3649T= , LRG_724t2:c.3649T=	NP_004439.2:p.Phe1217=
NR_110535.1:n.3973T=
XM_024450641.1:c.3787T=	XP_024306409.1:p.Phe1263=
XM_024450642.1:c.3742T=	XP_024306410.1:p.Phe1248=
XM_024450643.1:c.3697T=	XP_024306411.1:p.Phe1233=
NM_001005862.3:c.3559T=	NP_001005862.1:p.Phe1187=
NM_001289936.2:c.3604T=	NP_001276865.1:p.Phe1202=
NM_001289937.2:c.*228T=	NP_001276866.1:n.*228T=
NM_001382782.1:c.3559T=	NP_001369711.1:p.Phe1187=
NM_001382783.1:c.3559T=	NP_001369712.1:p.Phe1187=
NM_001382784.1:c.3766T=	NP_001369713.1:p.Phe1256=
NM_001382785.1:c.3751T=	NP_001369714.1:p.Phe1251=
NM_001382786.1:c.3730T=	NP_001369715.1:p.Phe1244=
NM_001382787.1:c.3724T=	NP_001369716.1:p.Phe1242=
NM_001382788.1:c.3679T=	NP_001369717.1:p.Phe1227=
NM_001382789.1:c.3670T=	NP_001369718.1:p.Phe1224=
NM_001382790.1:c.3646T=	NP_001369719.1:p.Phe1216=
NM_001382791.1:c.3640T=	NP_001369720.1:p.Phe1214=
NM_001382792.1:c.3613T=	NP_001369721.1:p.Phe1205=
NM_001382793.1:c.3607T=	NP_001369722.1:p.Phe1203=
NM_001382794.1:c.3607T=	NP_001369723.1:p.Phe1203=
NM_001382795.1:c.3601T=	NP_001369724.1:p.Phe1201=
NM_001382796.1:c.3562T=	NP_001369725.1:p.Phe1188=
NM_001382797.1:c.3550T=	NP_001369726.1:p.Phe1184=
NM_001382798.1:c.3493T=	NP_001369727.1:p.Phe1165=
NM_001382799.1:c.3469T=	NP_001369728.1:p.Phe1157=
NM_001382800.1:c.3463T=	NP_001369729.1:p.Phe1155=
NM_001382801.1:c.3445T=	NP_001369730.1:p.Phe1149=
NM_001382802.1:c.3391T=	NP_001369731.1:p.Phe1131=
NM_001382803.1:c.*228T=	NP_001369732.1:n.*228T=
NM_001382804.1:c.2821T=	NP_001369733.1:p.Phe941=
NM_001382805.1:c.2698T=	NP_001369734.1:p.Phe900=
NM_001382806.1:c.2611T=	NP_001369735.1:p.Phe871=
NM_004448.4:c.3649T= MANE Select	NP_004439.2:p.Phe1217=
NR_110535.2:n.3887T=