Canonical Allele Identifier: CA414706590

Gene: GPC3

Linked Data

• MyVariant Identifiers: chrX:g.132888086A>C (hg19) ; chrX:g.133754059A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133754059A>C , CM000685.2:g.133754059A>C	GRCh38
NC_000023.10:g.132888086A>C , CM000685.1:g.132888086A>C	GRCh37
NC_000023.9:g.132715752A>C	NCBI36
NG_009286.1:g.236581T>G , LRG_505:g.236581T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684880.1:c.*43T>G	ENSP00000510280.1:n.*43T>G
ENST00000689310.1:c.407T>G	ENSP00000510438.1:p.Val136Gly
ENST00000692630.1:n.585T>G
ENST00000370818.8:c.455T>G MANE Select	ENSP00000359854.3:p.Val152Gly
ENST00000394299.7:c.455T>G	ENSP00000377836.2:p.Val152Gly
ENST00000370818.7:c.455T>G	ENSP00000359854.3:p.Val152Gly
ENST00000394299.6:c.455T>G	ENSP00000377836.2:p.Val152Gly
ENST00000631057.2:c.293T>G	ENSP00000486325.1:p.Val98Gly
NM_001164617.1:c.455T>G	NP_001158089.1:p.Val152Gly
NM_001164618.1:c.407T>G	NP_001158090.1:p.Val136Gly
NM_001164619.1:c.293T>G	NP_001158091.1:p.Val98Gly
NM_004484.3:c.455T>G , LRG_505t1:c.455T>G	NP_004475.1:p.Val152Gly
XM_017029413.2:c.455T>G	XP_016884902.1:p.Val152Gly
NM_001164617.2:c.455T>G	NP_001158089.1:p.Val152Gly
NM_001164618.2:c.407T>G	NP_001158090.1:p.Val136Gly
NM_001164619.2:c.293T>G	NP_001158091.1:p.Val98Gly
NM_004484.4:c.455T>G MANE Select	NP_004475.1:p.Val152Gly