Canonical Allele Identifier: CA2459503237

Gene: GPC3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133753608G= , CM000685.2:g.133753608G=	GRCh38
NC_000023.10:g.132887635G= , CM000685.1:g.132887635G=	GRCh37
NC_000023.9:g.132715301G=	NCBI36
NG_009286.1:g.237032C= , LRG_505:g.237032C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406757.3:c.95C=
ENST00000684880.1:c.*494C=	ENSP00000510280.1:n.*494C=
ENST00000689310.1:c.858C=	ENSP00000510438.1:p.Ser286=
ENST00000692084.1:c.100C=
ENST00000370818.8:c.906C= MANE Select	ENSP00000359854.3:p.Ser302=
ENST00000394299.7:c.906C=	ENSP00000377836.2:p.Ser302=
ENST00000666673.1:n.100C=
ENST00000370818.7:c.906C=	ENSP00000359854.3:p.Ser302=
ENST00000394299.6:c.906C=	ENSP00000377836.2:p.Ser302=
ENST00000406757.2:c.95C=
ENST00000631057.2:c.744C=	ENSP00000486325.1:p.Ser248=
NM_001164617.1:c.906C=	NP_001158089.1:p.Ser302=
NM_001164618.1:c.858C=	NP_001158090.1:p.Ser286=
NM_001164619.1:c.744C=	NP_001158091.1:p.Ser248=
NM_004484.3:c.906C= , LRG_505t1:c.906C=	NP_004475.1:p.Ser302=
XM_017029413.2:c.906C=	XP_016884902.1:p.Ser302=
NM_001164617.2:c.906C=	NP_001158089.1:p.Ser302=
NM_001164618.2:c.858C=	NP_001158090.1:p.Ser286=
NM_001164619.2:c.744C=	NP_001158091.1:p.Ser248=
NM_004484.4:c.906C= MANE Select	NP_004475.1:p.Ser302=