Canonical Allele Identifier: CA2259229287

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727842G= , CM000679.2:g.39727842G=	GRCh38
NC_000017.10:g.37884095G= , CM000679.1:g.37884095G=	GRCh37
NC_000017.9:g.35137621G=	NCBI36
NG_007503.1:g.44703G= , LRG_724:g.44703G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3566G= MANE Select	ENSP00000269571.4:p.Gly1189=
ENST00000269571.9:c.3566G=	ENSP00000269571.4:p.Gly1189=
ENST00000406381.6:c.3476G=	ENSP00000385185.2:p.Gly1159=
ENST00000445658.6:c.2738G=	ENSP00000404047.2:p.Gly913=
ENST00000541774.5:c.3521G=	ENSP00000446466.1:p.Gly1174=
ENST00000578373.5:c.*3356G=	ENSP00000463427.1:n.*3356G=
ENST00000584450.5:c.*145G=	ENSP00000463714.1:n.*145G=
ENST00000584601.5:c.3476G=	ENSP00000462438.1:p.Gly1159=
NM_001005862.2:c.3476G= , LRG_724t1:c.3476G=	NP_001005862.1:p.Gly1159=
NM_001289936.1:c.3521G= , LRG_724t4:c.3521G=	NP_001276865.1:p.Gly1174=
NM_001289937.1:c.*145G=	NP_001276866.1:n.*145G=
NM_004448.3:c.3566G= , LRG_724t2:c.3566G=	NP_004439.2:p.Gly1189=
NR_110535.1:n.3890G=
XM_024450641.1:c.3704G=	XP_024306409.1:p.Gly1235=
XM_024450642.1:c.3659G=	XP_024306410.1:p.Gly1220=
XM_024450643.1:c.3614G=	XP_024306411.1:p.Gly1205=
NM_001005862.3:c.3476G=	NP_001005862.1:p.Gly1159=
NM_001289936.2:c.3521G=	NP_001276865.1:p.Gly1174=
NM_001289937.2:c.*145G=	NP_001276866.1:n.*145G=
NM_001382782.1:c.3476G=	NP_001369711.1:p.Gly1159=
NM_001382783.1:c.3476G=	NP_001369712.1:p.Gly1159=
NM_001382784.1:c.3683G=	NP_001369713.1:p.Gly1228=
NM_001382785.1:c.3668G=	NP_001369714.1:p.Gly1223=
NM_001382786.1:c.3647G=	NP_001369715.1:p.Gly1216=
NM_001382787.1:c.3641G=	NP_001369716.1:p.Gly1214=
NM_001382788.1:c.3596G=	NP_001369717.1:p.Gly1199=
NM_001382789.1:c.3587G=	NP_001369718.1:p.Gly1196=
NM_001382790.1:c.3563G=	NP_001369719.1:p.Gly1188=
NM_001382791.1:c.3557G=	NP_001369720.1:p.Gly1186=
NM_001382792.1:c.3530G=	NP_001369721.1:p.Gly1177=
NM_001382793.1:c.3524G=	NP_001369722.1:p.Gly1175=
NM_001382794.1:c.3524G=	NP_001369723.1:p.Gly1175=
NM_001382795.1:c.3518G=	NP_001369724.1:p.Gly1173=
NM_001382796.1:c.3479G=	NP_001369725.1:p.Gly1160=
NM_001382797.1:c.3467G=	NP_001369726.1:p.Gly1156=
NM_001382798.1:c.3410G=	NP_001369727.1:p.Gly1137=
NM_001382799.1:c.3386G=	NP_001369728.1:p.Gly1129=
NM_001382800.1:c.3380G=	NP_001369729.1:p.Gly1127=
NM_001382801.1:c.3362G=	NP_001369730.1:p.Gly1121=
NM_001382802.1:c.3308G=	NP_001369731.1:p.Gly1103=
NM_001382803.1:c.*145G=	NP_001369732.1:n.*145G=
NM_001382804.1:c.2738G=	NP_001369733.1:p.Gly913=
NM_001382805.1:c.2615G=	NP_001369734.1:p.Gly872=
NM_001382806.1:c.2528G=	NP_001369735.1:p.Gly843=
NM_004448.4:c.3566G= MANE Select	NP_004439.2:p.Gly1189=
NR_110535.2:n.3804G=