Canonical Allele Identifier: CA2459487436

Gene: GPC3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133699915T= , CM000685.2:g.133699915T=	GRCh38
NC_000023.10:g.132833943T= , CM000685.1:g.132833943T=	GRCh37
NC_000023.9:g.132661609T=	NCBI36
NG_009286.1:g.290724A= , LRG_505:g.290724A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406757.3:c.335A=
ENST00000666673.2:n.177A=
ENST00000684880.1:c.*734A=	ENSP00000510280.1:n.*734A=
ENST00000689310.1:c.1098A=	ENSP00000510438.1:p.Glu366=
ENST00000692084.1:c.433A=
ENST00000370818.8:c.1146A= MANE Select	ENSP00000359854.3:p.Glu382=
ENST00000394299.7:c.1215A=	ENSP00000377836.2:p.Glu405=
ENST00000666673.1:n.433A=
ENST00000667662.1:n.213A=
ENST00000669691.1:n.192A=
ENST00000370818.7:c.1146A=	ENSP00000359854.3:p.Glu382=
ENST00000394299.6:c.1215A=	ENSP00000377836.2:p.Glu405=
ENST00000406757.2:c.335A=
ENST00000631057.2:c.984A=	ENSP00000486325.1:p.Glu328=
NM_001164617.1:c.1215A=	NP_001158089.1:p.Glu405=
NM_001164618.1:c.1098A=	NP_001158090.1:p.Glu366=
NM_001164619.1:c.984A=	NP_001158091.1:p.Glu328=
NM_004484.3:c.1146A= , LRG_505t1:c.1146A=	NP_004475.1:p.Glu382=
XM_017029413.2:c.1146A=	XP_016884902.1:p.Glu382=
NM_001164617.2:c.1215A=	NP_001158089.1:p.Glu405=
NM_001164618.2:c.1098A=	NP_001158090.1:p.Glu366=
NM_001164619.2:c.984A=	NP_001158091.1:p.Glu328=
NM_004484.4:c.1146A= MANE Select	NP_004475.1:p.Glu382=