Canonical Allele Identifier: CA16616631

Gene: GPC3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133692402G>C , CM000685.2:g.133692402G>C	GRCh38
NC_000023.10:g.132826430G>C , CM000685.1:g.132826430G>C	GRCh37
NC_000023.9:g.132654096G>C	NCBI36
NG_009286.1:g.298237C>G , LRG_505:g.298237C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004484.4:c.1259C>G MANE Select	NP_004475.1:p.Thr420Ser
ENST00000370818.8:c.1259C>G MANE Select	ENSP00000359854.3:p.Thr420Ser
NM_001164617.1:c.1328C>G	NP_001158089.1:p.Thr443Ser
NM_001164617.2:c.1328C>G	NP_001158089.1:p.Thr443Ser
NM_001164618.1:c.1211C>G	NP_001158090.1:p.Thr404Ser
NM_001164618.2:c.1211C>G	NP_001158090.1:p.Thr404Ser
NM_001164619.1:c.1097C>G	NP_001158091.1:p.Thr366Ser
NM_001164619.2:c.1097C>G	NP_001158091.1:p.Thr366Ser
NM_004484.3:c.1259C>G , LRG_505t1:c.1259C>G	NP_004475.1:p.Thr420Ser
ENST00000370818.7:c.1259C>G	ENSP00000359854.3:p.Thr420Ser
ENST00000394299.6:c.1328C>G	ENSP00000377836.2:p.Thr443Ser
ENST00000394299.7:c.1328C>G	ENSP00000377836.2:p.Thr443Ser
ENST00000406757.2:c.448C>G
ENST00000406757.3:c.448C>G
ENST00000631057.2:c.1097C>G	ENSP00000486325.1:p.Thr366Ser
ENST00000666673.1:n.546C>G
ENST00000666673.2:n.290C>G
ENST00000667662.1:n.326C>G
ENST00000669691.1:n.325C>G
ENST00000684880.1:c.*847C>G	ENSP00000510280.1:n.*847C>G
ENST00000689310.1:c.1211C>G	ENSP00000510438.1:p.Thr404Ser
ENST00000692084.1:c.546C>G
XM_017029413.2:c.1259C>G	XP_016884902.1:p.Thr420Ser