Canonical Allele Identifier: CA2259229253

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727772A= , CM000679.2:g.39727772A=	GRCh38
NC_000017.10:g.37884025A= , CM000679.1:g.37884025A=	GRCh37
NC_000017.9:g.35137551A=	NCBI36
NG_007503.1:g.44633A= , LRG_724:g.44633A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3496A= MANE Select	ENSP00000269571.4:p.Thr1166=
ENST00000269571.9:c.3496A=	ENSP00000269571.4:p.Thr1166=
ENST00000406381.6:c.3406A=	ENSP00000385185.2:p.Thr1136=
ENST00000445658.6:c.2668A=	ENSP00000404047.2:p.Thr890=
ENST00000541774.5:c.3451A=	ENSP00000446466.1:p.Thr1151=
ENST00000578373.5:c.*3286A=	ENSP00000463427.1:n.*3286A=
ENST00000584450.5:c.*75A=	ENSP00000463714.1:n.*75A=
ENST00000584601.5:c.3406A=	ENSP00000462438.1:p.Thr1136=
NM_001005862.2:c.3406A= , LRG_724t1:c.3406A=	NP_001005862.1:p.Thr1136=
NM_001289936.1:c.3451A= , LRG_724t4:c.3451A=	NP_001276865.1:p.Thr1151=
NM_001289937.1:c.*75A=	NP_001276866.1:n.*75A=
NM_004448.3:c.3496A= , LRG_724t2:c.3496A=	NP_004439.2:p.Thr1166=
NR_110535.1:n.3820A=
XM_024450641.1:c.3634A=	XP_024306409.1:p.Thr1212=
XM_024450642.1:c.3589A=	XP_024306410.1:p.Thr1197=
XM_024450643.1:c.3544A=	XP_024306411.1:p.Thr1182=
NM_001005862.3:c.3406A=	NP_001005862.1:p.Thr1136=
NM_001289936.2:c.3451A=	NP_001276865.1:p.Thr1151=
NM_001289937.2:c.*75A=	NP_001276866.1:n.*75A=
NM_001382782.1:c.3406A=	NP_001369711.1:p.Thr1136=
NM_001382783.1:c.3406A=	NP_001369712.1:p.Thr1136=
NM_001382784.1:c.3613A=	NP_001369713.1:p.Thr1205=
NM_001382785.1:c.3598A=	NP_001369714.1:p.Thr1200=
NM_001382786.1:c.3577A=	NP_001369715.1:p.Thr1193=
NM_001382787.1:c.3571A=	NP_001369716.1:p.Thr1191=
NM_001382788.1:c.3526A=	NP_001369717.1:p.Thr1176=
NM_001382789.1:c.3517A=	NP_001369718.1:p.Thr1173=
NM_001382790.1:c.3493A=	NP_001369719.1:p.Thr1165=
NM_001382791.1:c.3487A=	NP_001369720.1:p.Thr1163=
NM_001382792.1:c.3460A=	NP_001369721.1:p.Thr1154=
NM_001382793.1:c.3454A=	NP_001369722.1:p.Thr1152=
NM_001382794.1:c.3454A=	NP_001369723.1:p.Thr1152=
NM_001382795.1:c.3448A=	NP_001369724.1:p.Thr1150=
NM_001382796.1:c.3409A=	NP_001369725.1:p.Thr1137=
NM_001382797.1:c.3397A=	NP_001369726.1:p.Thr1133=
NM_001382798.1:c.3340A=	NP_001369727.1:p.Thr1114=
NM_001382799.1:c.3316A=	NP_001369728.1:p.Thr1106=
NM_001382800.1:c.3310A=	NP_001369729.1:p.Thr1104=
NM_001382801.1:c.3292A=	NP_001369730.1:p.Thr1098=
NM_001382802.1:c.3238A=	NP_001369731.1:p.Thr1080=
NM_001382803.1:c.*75A=	NP_001369732.1:n.*75A=
NM_001382804.1:c.2668A=	NP_001369733.1:p.Thr890=
NM_001382805.1:c.2545A=	NP_001369734.1:p.Thr849=
NM_001382806.1:c.2458A=	NP_001369735.1:p.Thr820=
NM_004448.4:c.3496A= MANE Select	NP_004439.2:p.Thr1166=
NR_110535.2:n.3734A=