Canonical Allele Identifier: CA2259229329

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727951G= , CM000679.2:g.39727951G=	GRCh38
NC_000017.10:g.37884204G= , CM000679.1:g.37884204G=	GRCh37
NC_000017.9:g.35137730G=	NCBI36
NG_007503.1:g.44812G= , LRG_724:g.44812G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3675G= MANE Select	ENSP00000269571.4:p.Gln1225=
ENST00000269571.9:c.3675G=	ENSP00000269571.4:p.Gln1225=
ENST00000406381.6:c.3585G=	ENSP00000385185.2:p.Gln1195=
ENST00000445658.6:c.2847G=	ENSP00000404047.2:p.Gln949=
ENST00000541774.5:c.3630G=	ENSP00000446466.1:p.Gln1210=
ENST00000578373.5:c.*3465G=	ENSP00000463427.1:n.*3465G=
ENST00000584450.5:c.*254G=	ENSP00000463714.1:n.*254G=
ENST00000584601.5:c.3585G=	ENSP00000462438.1:p.Gln1195=
NM_001005862.2:c.3585G= , LRG_724t1:c.3585G=	NP_001005862.1:p.Gln1195=
NM_001289936.1:c.3630G= , LRG_724t4:c.3630G=	NP_001276865.1:p.Gln1210=
NM_001289937.1:c.*254G=	NP_001276866.1:n.*254G=
NM_004448.3:c.3675G= , LRG_724t2:c.3675G=	NP_004439.2:p.Gln1225=
NR_110535.1:n.3999G=
XM_024450641.1:c.3813G=	XP_024306409.1:p.Gln1271=
XM_024450642.1:c.3768G=	XP_024306410.1:p.Gln1256=
XM_024450643.1:c.3723G=	XP_024306411.1:p.Gln1241=
NM_001005862.3:c.3585G=	NP_001005862.1:p.Gln1195=
NM_001289936.2:c.3630G=	NP_001276865.1:p.Gln1210=
NM_001289937.2:c.*254G=	NP_001276866.1:n.*254G=
NM_001382782.1:c.3585G=	NP_001369711.1:p.Gln1195=
NM_001382783.1:c.3585G=	NP_001369712.1:p.Gln1195=
NM_001382784.1:c.3792G=	NP_001369713.1:p.Gln1264=
NM_001382785.1:c.3777G=	NP_001369714.1:p.Gln1259=
NM_001382786.1:c.3756G=	NP_001369715.1:p.Gln1252=
NM_001382787.1:c.3750G=	NP_001369716.1:p.Gln1250=
NM_001382788.1:c.3705G=	NP_001369717.1:p.Gln1235=
NM_001382789.1:c.3696G=	NP_001369718.1:p.Gln1232=
NM_001382790.1:c.3672G=	NP_001369719.1:p.Gln1224=
NM_001382791.1:c.3666G=	NP_001369720.1:p.Gln1222=
NM_001382792.1:c.3639G=	NP_001369721.1:p.Gln1213=
NM_001382793.1:c.3633G=	NP_001369722.1:p.Gln1211=
NM_001382794.1:c.3633G=	NP_001369723.1:p.Gln1211=
NM_001382795.1:c.3627G=	NP_001369724.1:p.Gln1209=
NM_001382796.1:c.3588G=	NP_001369725.1:p.Gln1196=
NM_001382797.1:c.3576G=	NP_001369726.1:p.Gln1192=
NM_001382798.1:c.3519G=	NP_001369727.1:p.Gln1173=
NM_001382799.1:c.3495G=	NP_001369728.1:p.Gln1165=
NM_001382800.1:c.3489G=	NP_001369729.1:p.Gln1163=
NM_001382801.1:c.3471G=	NP_001369730.1:p.Gln1157=
NM_001382802.1:c.3417G=	NP_001369731.1:p.Gln1139=
NM_001382803.1:c.*254G=	NP_001369732.1:n.*254G=
NM_001382804.1:c.2847G=	NP_001369733.1:p.Gln949=
NM_001382805.1:c.2724G=	NP_001369734.1:p.Gln908=
NM_001382806.1:c.2637G=	NP_001369735.1:p.Gln879=
NM_004448.4:c.3675G= MANE Select	NP_004439.2:p.Gln1225=
NR_110535.2:n.3913G=