Canonical Allele Identifier: CA2459503235

Gene: GPC3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133753604C= , CM000685.2:g.133753604C=	GRCh38
NC_000023.10:g.132887631C= , CM000685.1:g.132887631C=	GRCh37
NC_000023.9:g.132715297C=	NCBI36
NG_009286.1:g.237036G= , LRG_505:g.237036G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406757.3:c.99G=
ENST00000684880.1:c.*498G=	ENSP00000510280.1:n.*498G=
ENST00000689310.1:c.862G=	ENSP00000510438.1:p.Glu288=
ENST00000692084.1:c.104G=
ENST00000370818.8:c.910G= MANE Select	ENSP00000359854.3:p.Glu304=
ENST00000394299.7:c.910G=	ENSP00000377836.2:p.Glu304=
ENST00000666673.1:n.104G=
ENST00000370818.7:c.910G=	ENSP00000359854.3:p.Glu304=
ENST00000394299.6:c.910G=	ENSP00000377836.2:p.Glu304=
ENST00000406757.2:c.99G=
ENST00000631057.2:c.748G=	ENSP00000486325.1:p.Glu250=
NM_001164617.1:c.910G=	NP_001158089.1:p.Glu304=
NM_001164618.1:c.862G=	NP_001158090.1:p.Glu288=
NM_001164619.1:c.748G=	NP_001158091.1:p.Glu250=
NM_004484.3:c.910G= , LRG_505t1:c.910G=	NP_004475.1:p.Glu304=
XM_017029413.2:c.910G=	XP_016884902.1:p.Glu304=
NM_001164617.2:c.910G=	NP_001158089.1:p.Glu304=
NM_001164618.2:c.862G=	NP_001158090.1:p.Glu288=
NM_001164619.2:c.748G=	NP_001158091.1:p.Glu250=
NM_004484.4:c.910G= MANE Select	NP_004475.1:p.Glu304=