Canonical Allele Identifier: CA2259229284

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727837T= , CM000679.2:g.39727837T=	GRCh38
NC_000017.10:g.37884090T= , CM000679.1:g.37884090T=	GRCh37
NC_000017.9:g.35137616T=	NCBI36
NG_007503.1:g.44698T= , LRG_724:g.44698T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3561T= MANE Select	ENSP00000269571.4:p.Phe1187=
ENST00000269571.9:c.3561T=	ENSP00000269571.4:p.Phe1187=
ENST00000406381.6:c.3471T=	ENSP00000385185.2:p.Phe1157=
ENST00000445658.6:c.2733T=	ENSP00000404047.2:p.Phe911=
ENST00000541774.5:c.3516T=	ENSP00000446466.1:p.Phe1172=
ENST00000578373.5:c.*3351T=	ENSP00000463427.1:n.*3351T=
ENST00000584450.5:c.*140T=	ENSP00000463714.1:n.*140T=
ENST00000584601.5:c.3471T=	ENSP00000462438.1:p.Phe1157=
NM_001005862.2:c.3471T= , LRG_724t1:c.3471T=	NP_001005862.1:p.Phe1157=
NM_001289936.1:c.3516T= , LRG_724t4:c.3516T=	NP_001276865.1:p.Phe1172=
NM_001289937.1:c.*140T=	NP_001276866.1:n.*140T=
NM_004448.3:c.3561T= , LRG_724t2:c.3561T=	NP_004439.2:p.Phe1187=
NR_110535.1:n.3885T=
XM_024450641.1:c.3699T=	XP_024306409.1:p.Phe1233=
XM_024450642.1:c.3654T=	XP_024306410.1:p.Phe1218=
XM_024450643.1:c.3609T=	XP_024306411.1:p.Phe1203=
NM_001005862.3:c.3471T=	NP_001005862.1:p.Phe1157=
NM_001289936.2:c.3516T=	NP_001276865.1:p.Phe1172=
NM_001289937.2:c.*140T=	NP_001276866.1:n.*140T=
NM_001382782.1:c.3471T=	NP_001369711.1:p.Phe1157=
NM_001382783.1:c.3471T=	NP_001369712.1:p.Phe1157=
NM_001382784.1:c.3678T=	NP_001369713.1:p.Phe1226=
NM_001382785.1:c.3663T=	NP_001369714.1:p.Phe1221=
NM_001382786.1:c.3642T=	NP_001369715.1:p.Phe1214=
NM_001382787.1:c.3636T=	NP_001369716.1:p.Phe1212=
NM_001382788.1:c.3591T=	NP_001369717.1:p.Phe1197=
NM_001382789.1:c.3582T=	NP_001369718.1:p.Phe1194=
NM_001382790.1:c.3558T=	NP_001369719.1:p.Phe1186=
NM_001382791.1:c.3552T=	NP_001369720.1:p.Phe1184=
NM_001382792.1:c.3525T=	NP_001369721.1:p.Phe1175=
NM_001382793.1:c.3519T=	NP_001369722.1:p.Phe1173=
NM_001382794.1:c.3519T=	NP_001369723.1:p.Phe1173=
NM_001382795.1:c.3513T=	NP_001369724.1:p.Phe1171=
NM_001382796.1:c.3474T=	NP_001369725.1:p.Phe1158=
NM_001382797.1:c.3462T=	NP_001369726.1:p.Phe1154=
NM_001382798.1:c.3405T=	NP_001369727.1:p.Phe1135=
NM_001382799.1:c.3381T=	NP_001369728.1:p.Phe1127=
NM_001382800.1:c.3375T=	NP_001369729.1:p.Phe1125=
NM_001382801.1:c.3357T=	NP_001369730.1:p.Phe1119=
NM_001382802.1:c.3303T=	NP_001369731.1:p.Phe1101=
NM_001382803.1:c.*140T=	NP_001369732.1:n.*140T=
NM_001382804.1:c.2733T=	NP_001369733.1:p.Phe911=
NM_001382805.1:c.2610T=	NP_001369734.1:p.Phe870=
NM_001382806.1:c.2523T=	NP_001369735.1:p.Phe841=
NM_004448.4:c.3561T= MANE Select	NP_004439.2:p.Phe1187=
NR_110535.2:n.3799T=