Canonical Allele Identifier: CA16043214
Gene: GPC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 372372
ClinVar RCV Id: RCV000413842
dbSNP Id: rs1057517739
MyVariant Identifiers: chrX:g.133119302C>A (hg19) chrX:g.133985275C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.133985275C>A , CM000685.2:g.133985275C>A GRCh38
NC_000023.10:g.133119302C>A , CM000685.1:g.133119302C>A GRCh37
NC_000023.9:g.132946968C>A NCBI36
NG_009286.1:g.5365G>T , LRG_505:g.5365G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000684880.1:c.175G>T ENSP00000510280.1:p.Gly59Ter
ENST00000689310.1:c.175G>T ENSP00000510438.1:p.Gly59Ter
ENST00000692630.1:n.305G>T
ENST00000370818.8:c.175G>T MANE Select ENSP00000359854.3:p.Gly59Ter
ENST00000394299.7:c.175G>T ENSP00000377836.2:p.Gly59Ter
ENST00000370818.7:c.175G>T ENSP00000359854.3:p.Gly59Ter
ENST00000394299.6:c.175G>T ENSP00000377836.2:p.Gly59Ter
ENST00000631057.2:c.175G>T ENSP00000486325.1:p.Glu59Ter
NM_001164617.1:c.175G>T NP_001158089.1:p.Gly59Ter
NM_001164618.1:c.175G>T NP_001158090.1:p.Gly59Ter
NM_001164619.1:c.175G>T NP_001158091.1:p.Glu59Ter
NM_004484.3:c.175G>T , LRG_505t1:c.175G>T NP_004475.1:p.Gly59Ter
XM_017029413.2:c.175G>T XP_016884902.1:p.Gly59Ter
NM_001164617.2:c.175G>T NP_001158089.1:p.Gly59Ter
NM_001164618.2:c.175G>T NP_001158090.1:p.Gly59Ter
NM_001164619.2:c.175G>T NP_001158091.1:p.Glu59Ter
NM_004484.4:c.175G>T MANE Select NP_004475.1:p.Gly59Ter
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