Canonical Allele Identifier: CA2459487429

Gene: GPC3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133699902G= , CM000685.2:g.133699902G=	GRCh38
NC_000023.10:g.132833930G= , CM000685.1:g.132833930G=	GRCh37
NC_000023.9:g.132661596G=	NCBI36
NG_009286.1:g.290737C= , LRG_505:g.290737C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406757.3:c.348C=
ENST00000666673.2:n.190C=
ENST00000684880.1:c.*747C=	ENSP00000510280.1:n.*747C=
ENST00000689310.1:c.1111C=	ENSP00000510438.1:p.Arg371=
ENST00000692084.1:c.446C=
ENST00000370818.8:c.1159C= MANE Select	ENSP00000359854.3:p.Arg387=
ENST00000394299.7:c.1228C=	ENSP00000377836.2:p.Arg410=
ENST00000666673.1:n.446C=
ENST00000667662.1:n.226C=
ENST00000669691.1:n.205C=
ENST00000370818.7:c.1159C=	ENSP00000359854.3:p.Arg387=
ENST00000394299.6:c.1228C=	ENSP00000377836.2:p.Arg410=
ENST00000406757.2:c.348C=
ENST00000631057.2:c.997C=	ENSP00000486325.1:p.Arg333=
NM_001164617.1:c.1228C=	NP_001158089.1:p.Arg410=
NM_001164618.1:c.1111C=	NP_001158090.1:p.Arg371=
NM_001164619.1:c.997C=	NP_001158091.1:p.Arg333=
NM_004484.3:c.1159C= , LRG_505t1:c.1159C=	NP_004475.1:p.Arg387=
XM_017029413.2:c.1159C=	XP_016884902.1:p.Arg387=
NM_001164617.2:c.1228C=	NP_001158089.1:p.Arg410=
NM_001164618.2:c.1111C=	NP_001158090.1:p.Arg371=
NM_001164619.2:c.997C=	NP_001158091.1:p.Arg333=
NM_004484.4:c.1159C= MANE Select	NP_004475.1:p.Arg387=