Canonical Allele Identifier: CA414702626

Gene: GPC3

Genomic Alleles

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

Transcript Alleles

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