Canonical Allele Identifier: CA2259229324

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727938A= , CM000679.2:g.39727938A=	GRCh38
NC_000017.10:g.37884191A= , CM000679.1:g.37884191A=	GRCh37
NC_000017.9:g.35137717A=	NCBI36
NG_007503.1:g.44799A= , LRG_724:g.44799A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3662A= MANE Select	ENSP00000269571.4:p.Tyr1221=
ENST00000269571.9:c.3662A=	ENSP00000269571.4:p.Tyr1221=
ENST00000406381.6:c.3572A=	ENSP00000385185.2:p.Tyr1191=
ENST00000445658.6:c.2834A=	ENSP00000404047.2:p.Tyr945=
ENST00000541774.5:c.3617A=	ENSP00000446466.1:p.Tyr1206=
ENST00000578373.5:c.*3452A=	ENSP00000463427.1:n.*3452A=
ENST00000584450.5:c.*241A=	ENSP00000463714.1:n.*241A=
ENST00000584601.5:c.3572A=	ENSP00000462438.1:p.Tyr1191=
NM_001005862.2:c.3572A= , LRG_724t1:c.3572A=	NP_001005862.1:p.Tyr1191=
NM_001289936.1:c.3617A= , LRG_724t4:c.3617A=	NP_001276865.1:p.Tyr1206=
NM_001289937.1:c.*241A=	NP_001276866.1:n.*241A=
NM_004448.3:c.3662A= , LRG_724t2:c.3662A=	NP_004439.2:p.Tyr1221=
NR_110535.1:n.3986A=
XM_024450641.1:c.3800A=	XP_024306409.1:p.Tyr1267=
XM_024450642.1:c.3755A=	XP_024306410.1:p.Tyr1252=
XM_024450643.1:c.3710A=	XP_024306411.1:p.Tyr1237=
NM_001005862.3:c.3572A=	NP_001005862.1:p.Tyr1191=
NM_001289936.2:c.3617A=	NP_001276865.1:p.Tyr1206=
NM_001289937.2:c.*241A=	NP_001276866.1:n.*241A=
NM_001382782.1:c.3572A=	NP_001369711.1:p.Tyr1191=
NM_001382783.1:c.3572A=	NP_001369712.1:p.Tyr1191=
NM_001382784.1:c.3779A=	NP_001369713.1:p.Tyr1260=
NM_001382785.1:c.3764A=	NP_001369714.1:p.Tyr1255=
NM_001382786.1:c.3743A=	NP_001369715.1:p.Tyr1248=
NM_001382787.1:c.3737A=	NP_001369716.1:p.Tyr1246=
NM_001382788.1:c.3692A=	NP_001369717.1:p.Tyr1231=
NM_001382789.1:c.3683A=	NP_001369718.1:p.Tyr1228=
NM_001382790.1:c.3659A=	NP_001369719.1:p.Tyr1220=
NM_001382791.1:c.3653A=	NP_001369720.1:p.Tyr1218=
NM_001382792.1:c.3626A=	NP_001369721.1:p.Tyr1209=
NM_001382793.1:c.3620A=	NP_001369722.1:p.Tyr1207=
NM_001382794.1:c.3620A=	NP_001369723.1:p.Tyr1207=
NM_001382795.1:c.3614A=	NP_001369724.1:p.Tyr1205=
NM_001382796.1:c.3575A=	NP_001369725.1:p.Tyr1192=
NM_001382797.1:c.3563A=	NP_001369726.1:p.Tyr1188=
NM_001382798.1:c.3506A=	NP_001369727.1:p.Tyr1169=
NM_001382799.1:c.3482A=	NP_001369728.1:p.Tyr1161=
NM_001382800.1:c.3476A=	NP_001369729.1:p.Tyr1159=
NM_001382801.1:c.3458A=	NP_001369730.1:p.Tyr1153=
NM_001382802.1:c.3404A=	NP_001369731.1:p.Tyr1135=
NM_001382803.1:c.*241A=	NP_001369732.1:n.*241A=
NM_001382804.1:c.2834A=	NP_001369733.1:p.Tyr945=
NM_001382805.1:c.2711A=	NP_001369734.1:p.Tyr904=
NM_001382806.1:c.2624A=	NP_001369735.1:p.Tyr875=
NM_004448.4:c.3662A= MANE Select	NP_004439.2:p.Tyr1221=
NR_110535.2:n.3900A=