Canonical Allele Identifier: CA256006
Gene: GPC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.133536201C>T , CM000685.2:g.133536201C>T GRCh38
NC_000023.10:g.132670229C>T , CM000685.1:g.132670229C>T GRCh37
NC_000023.9:g.132497895C>T NCBI36
NG_009286.1:g.454438G>A , LRG_505:g.454438G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000406757.3:c.855G>A
ENST00000666673.2:n.697G>A
ENST00000689310.1:c.1618G>A ENSP00000510438.1:p.Gly540Arg
ENST00000692074.1:n.610G>A
ENST00000692084.1:c.953G>A
ENST00000370818.8:c.1666G>A MANE Select ENSP00000359854.3:p.Gly556Arg
ENST00000394299.7:c.1735G>A ENSP00000377836.2:p.Gly579Arg
ENST00000666017.1:n.544G>A
ENST00000666673.1:n.953G>A
ENST00000667662.1:n.733G>A
ENST00000669691.1:n.732G>A
ENST00000370818.7:c.1666G>A ENSP00000359854.3:p.Gly556Arg
ENST00000394299.6:c.1735G>A ENSP00000377836.2:p.Gly579Arg
ENST00000631057.2:c.1504G>A ENSP00000486325.1:p.Gly502Arg
NM_001164617.1:c.1735G>A NP_001158089.1:p.Gly579Arg
NM_001164618.1:c.1618G>A NP_001158090.1:p.Gly540Arg
NM_001164619.1:c.1504G>A NP_001158091.1:p.Gly502Arg
NM_004484.3:c.1666G>A , LRG_505t1:c.1666G>A NP_004475.1:p.Gly556Arg
NM_001164617.2:c.1735G>A NP_001158089.1:p.Gly579Arg
NM_001164618.2:c.1618G>A NP_001158090.1:p.Gly540Arg
NM_001164619.2:c.1504G>A NP_001158091.1:p.Gly502Arg
NM_004484.4:c.1666G>A MANE Select NP_004475.1:p.Gly556Arg