Canonical Allele Identifier: CA414704759

Gene: GPC3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133661825C>T , CM000685.2:g.133661825C>T	GRCh38
NC_000023.10:g.132795853C>T , CM000685.1:g.132795853C>T	GRCh37
NC_000023.9:g.132623519C>T	NCBI36
NG_009286.1:g.328814G>A , LRG_505:g.328814G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004484.4:c.1318G>A MANE Select	NP_004475.1:p.Gly440Arg
ENST00000370818.8:c.1318G>A MANE Select	ENSP00000359854.3:p.Gly440Arg
NM_001164617.1:c.1387G>A	NP_001158089.1:p.Gly463Arg
NM_001164617.2:c.1387G>A	NP_001158089.1:p.Gly463Arg
NM_001164618.1:c.1270G>A	NP_001158090.1:p.Gly424Arg
NM_001164618.2:c.1270G>A	NP_001158090.1:p.Gly424Arg
NM_001164619.1:c.1156G>A	NP_001158091.1:p.Gly386Arg
NM_001164619.2:c.1156G>A	NP_001158091.1:p.Gly386Arg
NM_004484.3:c.1318G>A , LRG_505t1:c.1318G>A	NP_004475.1:p.Gly440Arg
ENST00000370818.7:c.1318G>A	ENSP00000359854.3:p.Gly440Arg
ENST00000394299.6:c.1387G>A	ENSP00000377836.2:p.Gly463Arg
ENST00000394299.7:c.1387G>A	ENSP00000377836.2:p.Gly463Arg
ENST00000406757.2:c.507G>A
ENST00000406757.3:c.507G>A
ENST00000631057.2:c.1156G>A	ENSP00000486325.1:p.Gly386Arg
ENST00000666017.1:n.196G>A
ENST00000666673.1:n.605G>A
ENST00000666673.2:n.349G>A
ENST00000667662.1:n.385G>A
ENST00000669691.1:n.384G>A
ENST00000689310.1:c.1270G>A	ENSP00000510438.1:p.Gly424Arg
ENST00000692074.1:n.262G>A
ENST00000692084.1:c.605G>A