Canonical Allele Identifier: CA414705850

Gene: GPC3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133692495C>T , CM000685.2:g.133692495C>T	GRCh38
NC_000023.10:g.132826523C>T , CM000685.1:g.132826523C>T	GRCh37
NC_000023.9:g.132654189C>T	NCBI36
NG_009286.1:g.298144G>A , LRG_505:g.298144G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004484.4:c.1167-1G>A MANE Select	NP_004475.1:n.1167-1G>A
ENST00000370818.8:c.1167-1G>A MANE Select	ENSP00000359854.3:n.1167-1G>A
NM_001164617.1:c.1236-1G>A	NP_001158089.1:n.1236-1G>A
NM_001164617.2:c.1236-1G>A	NP_001158089.1:n.1236-1G>A
NM_001164618.1:c.1119-1G>A	NP_001158090.1:n.1119-1G>A
NM_001164618.2:c.1119-1G>A	NP_001158090.1:n.1119-1G>A
NM_001164619.1:c.1005-1G>A	NP_001158091.1:n.1005-1G>A
NM_001164619.2:c.1005-1G>A	NP_001158091.1:n.1005-1G>A
NM_004484.3:c.1167-1G>A , LRG_505t1:c.1167-1G>A	NP_004475.1:n.1167-1G>A
ENST00000370818.7:c.1167-1G>A	ENSP00000359854.3:n.1167-1G>A
ENST00000394299.6:c.1236-1G>A	ENSP00000377836.2:n.1236-1G>A
ENST00000394299.7:c.1236-1G>A	ENSP00000377836.2:n.1236-1G>A
ENST00000406757.2:c.356-1G>A
ENST00000406757.3:c.356-1G>A
ENST00000631057.2:c.1005-1G>A	ENSP00000486325.1:n.1005-1G>A
ENST00000666673.1:n.454-1G>A
ENST00000666673.2:n.198-1G>A
ENST00000667662.1:n.234-1G>A
ENST00000669691.1:n.232G>A
ENST00000684880.1:c.*755-1G>A	ENSP00000510280.1:n.*755-1G>A
ENST00000689310.1:c.1119-1G>A	ENSP00000510438.1:n.1119-1G>A
ENST00000692084.1:c.454-1G>A
XM_017029413.2:c.1167-1G>A	XP_016884902.1:n.1167-1G>A