Canonical Allele Identifier: CA335966670

Gene: GPC3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133536251C>G , CM000685.2:g.133536251C>G	GRCh38
NC_000023.10:g.132670279C>G , CM000685.1:g.132670279C>G	GRCh37
NC_000023.9:g.132497945C>G	NCBI36
NG_009286.1:g.454388G>C , LRG_505:g.454388G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_004484.4:c.1616G>C MANE Select	NP_004475.1:p.Ser539Thr
ENST00000370818.8:c.1616G>C MANE Select	ENSP00000359854.3:p.Ser539Thr
NM_001164617.1:c.1685G>C	NP_001158089.1:p.Ser562Thr
NM_001164617.2:c.1685G>C	NP_001158089.1:p.Ser562Thr
NM_001164618.1:c.1568G>C	NP_001158090.1:p.Ser523Thr
NM_001164618.2:c.1568G>C	NP_001158090.1:p.Ser523Thr
NM_001164619.1:c.1454G>C	NP_001158091.1:p.Ser485Thr
NM_001164619.2:c.1454G>C	NP_001158091.1:p.Ser485Thr
NM_004484.3:c.1616G>C , LRG_505t1:c.1616G>C	NP_004475.1:p.Ser539Thr
ENST00000370818.7:c.1616G>C	ENSP00000359854.3:p.Ser539Thr
ENST00000394299.6:c.1685G>C	ENSP00000377836.2:p.Ser562Thr
ENST00000394299.7:c.1685G>C	ENSP00000377836.2:p.Ser562Thr
ENST00000406757.3:c.805G>C
ENST00000631057.2:c.1454G>C	ENSP00000486325.1:p.Ser485Thr
ENST00000666017.1:n.494G>C
ENST00000666673.1:n.903G>C
ENST00000666673.2:n.647G>C
ENST00000667662.1:n.683G>C
ENST00000669691.1:n.682G>C
ENST00000689310.1:c.1568G>C	ENSP00000510438.1:p.Ser523Thr
ENST00000692074.1:n.560G>C
ENST00000692084.1:c.903G>C