Canonical Allele Identifier: CA2459503218

Gene: GPC3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133753560G= , CM000685.2:g.133753560G=	GRCh38
NC_000023.10:g.132887587G= , CM000685.1:g.132887587G=	GRCh37
NC_000023.9:g.132715253G=	NCBI36
NG_009286.1:g.237080C= , LRG_505:g.237080C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406757.3:c.143C=
ENST00000684880.1:c.*542C=	ENSP00000510280.1:n.*542C=
ENST00000689310.1:c.906C=	ENSP00000510438.1:p.Asn302=
ENST00000692084.1:c.148C=
ENST00000370818.8:c.954C= MANE Select	ENSP00000359854.3:p.Asn318=
ENST00000394299.7:c.954C=	ENSP00000377836.2:p.Asn318=
ENST00000666673.1:n.148C=
ENST00000370818.7:c.954C=	ENSP00000359854.3:p.Asn318=
ENST00000394299.6:c.954C=	ENSP00000377836.2:p.Asn318=
ENST00000406757.2:c.143C=
ENST00000631057.2:c.792C=	ENSP00000486325.1:p.Asn264=
NM_001164617.1:c.954C=	NP_001158089.1:p.Asn318=
NM_001164618.1:c.906C=	NP_001158090.1:p.Asn302=
NM_001164619.1:c.792C=	NP_001158091.1:p.Asn264=
NM_004484.3:c.954C= , LRG_505t1:c.954C=	NP_004475.1:p.Asn318=
XM_017029413.2:c.954C=	XP_016884902.1:p.Asn318=
NM_001164617.2:c.954C=	NP_001158089.1:p.Asn318=
NM_001164618.2:c.906C=	NP_001158090.1:p.Asn302=
NM_001164619.2:c.792C=	NP_001158091.1:p.Asn264=
NM_004484.4:c.954C= MANE Select	NP_004475.1:p.Asn318=