Canonical Allele Identifier: CA644541561

Gene: GPC3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133692363G>A , CM000685.2:g.133692363G>A	GRCh38
NC_000023.10:g.132826391G>A , CM000685.1:g.132826391G>A	GRCh37
NC_000023.9:g.132654057G>A	NCBI36
NG_009286.1:g.298276C>T , LRG_505:g.298276C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406757.3:c.481+6C>T
ENST00000666673.2:n.323+6C>T
ENST00000684880.1:c.*886C>T	ENSP00000510280.1:n.*886C>T
ENST00000689310.1:c.1244+6C>T	ENSP00000510438.1:n.1244+6C>T
ENST00000692084.1:c.579+6C>T
ENST00000370818.8:c.1292+6C>T MANE Select	ENSP00000359854.3:n.1292+6C>T
ENST00000394299.7:c.1361+6C>T	ENSP00000377836.2:n.1361+6C>T
ENST00000666673.1:n.579+6C>T
ENST00000667662.1:n.359+6C>T
ENST00000669691.1:n.358+6C>T
ENST00000370818.7:c.1292+6C>T	ENSP00000359854.3:n.1292+6C>T
ENST00000394299.6:c.1361+6C>T	ENSP00000377836.2:n.1361+6C>T
ENST00000406757.2:c.481+6C>T
ENST00000631057.2:c.1130+6C>T	ENSP00000486325.1:n.1130+6C>T
NM_001164617.1:c.1361+6C>T	NP_001158089.1:n.1361+6C>T
NM_001164618.1:c.1244+6C>T	NP_001158090.1:n.1244+6C>T
NM_001164619.1:c.1130+6C>T	NP_001158091.1:n.1130+6C>T
NM_004484.3:c.1292+6C>T , LRG_505t1:c.1292+6C>T	NP_004475.1:n.1292+6C>T
XM_017029413.2:c.1292+6C>T	XP_016884902.1:n.1292+6C>T
NM_001164617.2:c.1361+6C>T	NP_001158089.1:n.1361+6C>T
NM_001164618.2:c.1244+6C>T	NP_001158090.1:n.1244+6C>T
NM_001164619.2:c.1130+6C>T	NP_001158091.1:n.1130+6C>T
NM_004484.4:c.1292+6C>T MANE Select	NP_004475.1:n.1292+6C>T