Canonical Allele Identifier: CA414701497

Gene: GPC3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133596559T>G , CM000685.2:g.133596559T>G	GRCh38
NC_000023.10:g.132730587T>G , CM000685.1:g.132730587T>G	GRCh37
NC_000023.9:g.132558253T>G	NCBI36
NG_009286.1:g.394080A>C , LRG_505:g.394080A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406757.3:c.643A>C
ENST00000666673.2:n.485A>C
ENST00000689310.1:c.1406A>C	ENSP00000510438.1:p.Asp469Ala
ENST00000692074.1:n.398A>C
ENST00000692084.1:c.741A>C
ENST00000370818.8:c.1454A>C MANE Select	ENSP00000359854.3:p.Asp485Ala
ENST00000394299.7:c.1523A>C	ENSP00000377836.2:p.Asp508Ala
ENST00000666017.1:n.332A>C
ENST00000666673.1:n.741A>C
ENST00000667662.1:n.521A>C
ENST00000669691.1:n.520A>C
ENST00000370818.7:c.1454A>C	ENSP00000359854.3:p.Asp485Ala
ENST00000394299.6:c.1523A>C	ENSP00000377836.2:p.Asp508Ala
ENST00000406757.2:c.643A>C
ENST00000631057.2:c.1292A>C	ENSP00000486325.1:p.Asp431Ala
NM_001164617.1:c.1523A>C	NP_001158089.1:p.Asp508Ala
NM_001164618.1:c.1406A>C	NP_001158090.1:p.Asp469Ala
NM_001164619.1:c.1292A>C	NP_001158091.1:p.Asp431Ala
NM_004484.3:c.1454A>C , LRG_505t1:c.1454A>C	NP_004475.1:p.Asp485Ala
NM_001164617.2:c.1523A>C	NP_001158089.1:p.Asp508Ala
NM_001164618.2:c.1406A>C	NP_001158090.1:p.Asp469Ala
NM_001164619.2:c.1292A>C	NP_001158091.1:p.Asp431Ala
NM_004484.4:c.1454A>C MANE Select	NP_004475.1:p.Asp485Ala