Canonical Allele Identifier: CA2259229286

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727841G= , CM000679.2:g.39727841G=	GRCh38
NC_000017.10:g.37884094G= , CM000679.1:g.37884094G=	GRCh37
NC_000017.9:g.35137620G=	NCBI36
NG_007503.1:g.44702G= , LRG_724:g.44702G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3565G= MANE Select	ENSP00000269571.4:p.Gly1189=
ENST00000269571.9:c.3565G=	ENSP00000269571.4:p.Gly1189=
ENST00000406381.6:c.3475G=	ENSP00000385185.2:p.Gly1159=
ENST00000445658.6:c.2737G=	ENSP00000404047.2:p.Gly913=
ENST00000541774.5:c.3520G=	ENSP00000446466.1:p.Gly1174=
ENST00000578373.5:c.*3355G=	ENSP00000463427.1:n.*3355G=
ENST00000584450.5:c.*144G=	ENSP00000463714.1:n.*144G=
ENST00000584601.5:c.3475G=	ENSP00000462438.1:p.Gly1159=
NM_001005862.2:c.3475G= , LRG_724t1:c.3475G=	NP_001005862.1:p.Gly1159=
NM_001289936.1:c.3520G= , LRG_724t4:c.3520G=	NP_001276865.1:p.Gly1174=
NM_001289937.1:c.*144G=	NP_001276866.1:n.*144G=
NM_004448.3:c.3565G= , LRG_724t2:c.3565G=	NP_004439.2:p.Gly1189=
NR_110535.1:n.3889G=
XM_024450641.1:c.3703G=	XP_024306409.1:p.Gly1235=
XM_024450642.1:c.3658G=	XP_024306410.1:p.Gly1220=
XM_024450643.1:c.3613G=	XP_024306411.1:p.Gly1205=
NM_001005862.3:c.3475G=	NP_001005862.1:p.Gly1159=
NM_001289936.2:c.3520G=	NP_001276865.1:p.Gly1174=
NM_001289937.2:c.*144G=	NP_001276866.1:n.*144G=
NM_001382782.1:c.3475G=	NP_001369711.1:p.Gly1159=
NM_001382783.1:c.3475G=	NP_001369712.1:p.Gly1159=
NM_001382784.1:c.3682G=	NP_001369713.1:p.Gly1228=
NM_001382785.1:c.3667G=	NP_001369714.1:p.Gly1223=
NM_001382786.1:c.3646G=	NP_001369715.1:p.Gly1216=
NM_001382787.1:c.3640G=	NP_001369716.1:p.Gly1214=
NM_001382788.1:c.3595G=	NP_001369717.1:p.Gly1199=
NM_001382789.1:c.3586G=	NP_001369718.1:p.Gly1196=
NM_001382790.1:c.3562G=	NP_001369719.1:p.Gly1188=
NM_001382791.1:c.3556G=	NP_001369720.1:p.Gly1186=
NM_001382792.1:c.3529G=	NP_001369721.1:p.Gly1177=
NM_001382793.1:c.3523G=	NP_001369722.1:p.Gly1175=
NM_001382794.1:c.3523G=	NP_001369723.1:p.Gly1175=
NM_001382795.1:c.3517G=	NP_001369724.1:p.Gly1173=
NM_001382796.1:c.3478G=	NP_001369725.1:p.Gly1160=
NM_001382797.1:c.3466G=	NP_001369726.1:p.Gly1156=
NM_001382798.1:c.3409G=	NP_001369727.1:p.Gly1137=
NM_001382799.1:c.3385G=	NP_001369728.1:p.Gly1129=
NM_001382800.1:c.3379G=	NP_001369729.1:p.Gly1127=
NM_001382801.1:c.3361G=	NP_001369730.1:p.Gly1121=
NM_001382802.1:c.3307G=	NP_001369731.1:p.Gly1103=
NM_001382803.1:c.*144G=	NP_001369732.1:n.*144G=
NM_001382804.1:c.2737G=	NP_001369733.1:p.Gly913=
NM_001382805.1:c.2614G=	NP_001369734.1:p.Gly872=
NM_001382806.1:c.2527G=	NP_001369735.1:p.Gly843=
NM_004448.4:c.3565G= MANE Select	NP_004439.2:p.Gly1189=
NR_110535.2:n.3803G=