Canonical Allele Identifier: CA414700682

Gene: GPC3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133596451C>T , CM000685.2:g.133596451C>T	GRCh38
NC_000023.10:g.132730479C>T , CM000685.1:g.132730479C>T	GRCh37
NC_000023.9:g.132558145C>T	NCBI36
NG_009286.1:g.394188G>A , LRG_505:g.394188G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406757.3:c.751G>A
ENST00000666673.2:n.593G>A
ENST00000689310.1:c.1514G>A	ENSP00000510438.1:p.Arg505His
ENST00000692074.1:n.506G>A
ENST00000692084.1:c.849G>A
ENST00000370818.8:c.1562G>A MANE Select	ENSP00000359854.3:p.Arg521His
ENST00000394299.7:c.1631G>A	ENSP00000377836.2:p.Arg544His
ENST00000666017.1:n.440G>A
ENST00000666673.1:n.849G>A
ENST00000667662.1:n.629G>A
ENST00000669691.1:n.628G>A
ENST00000370818.7:c.1562G>A	ENSP00000359854.3:p.Arg521His
ENST00000394299.6:c.1631G>A	ENSP00000377836.2:p.Arg544His
ENST00000406757.2:c.751G>A
ENST00000631057.2:c.1400G>A	ENSP00000486325.1:p.Arg467His
NM_001164617.1:c.1631G>A	NP_001158089.1:p.Arg544His
NM_001164618.1:c.1514G>A	NP_001158090.1:p.Arg505His
NM_001164619.1:c.1400G>A	NP_001158091.1:p.Arg467His
NM_004484.3:c.1562G>A , LRG_505t1:c.1562G>A	NP_004475.1:p.Arg521His
NM_001164617.2:c.1631G>A	NP_001158089.1:p.Arg544His
NM_001164618.2:c.1514G>A	NP_001158090.1:p.Arg505His
NM_001164619.2:c.1400G>A	NP_001158091.1:p.Arg467His
NM_004484.4:c.1562G>A MANE Select	NP_004475.1:p.Arg521His