Canonical Allele Identifier: CA10520851

Gene: GPC3

Linked Data

• dbSNP Id: rs745600849
• ExAC: X:132888222 A / AG
• gnomAD v2: X-132888222-A-AG
• gnomAD v3: X-133754195-A-AG
• gnomAD v4: X-133754195-A-AG
• MyVariant Identifiers: chrX:g.132888222_132888223insG (hg19) ; chrX:g.133754195_133754196insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133754195_133754196insG , CM000685.2:g.133754195_133754196insG	GRCh38
NC_000023.10:g.132888222_132888223insG , CM000685.1:g.132888222_132888223insG	GRCh37
NC_000023.9:g.132715888_132715889insG	NCBI36
NG_009286.1:g.236444_236445insC , LRG_505:g.236444_236445insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684880.1:c.409-20_409-19insC	ENSP00000510280.1:n.409-20_409-19insC
ENST00000689310.1:c.290-20_290-19insC	ENSP00000510438.1:n.290-20_290-19insC
ENST00000692630.1:n.468-20_468-19insC
ENST00000370818.8:c.338-20_338-19insC MANE Select	ENSP00000359854.3:n.338-20_338-19insC
ENST00000394299.7:c.338-20_338-19insC	ENSP00000377836.2:n.338-20_338-19insC
ENST00000370818.7:c.338-20_338-19insC	ENSP00000359854.3:n.338-20_338-19insC
ENST00000394299.6:c.338-20_338-19insC	ENSP00000377836.2:n.338-20_338-19insC
ENST00000631057.2:c.176-20_176-19insC	ENSP00000486325.1:n.176-20_176-19insC
NM_001164617.1:c.338-20_338-19insC	NP_001158089.1:n.338-20_338-19insC
NM_001164618.1:c.290-20_290-19insC	NP_001158090.1:n.290-20_290-19insC
NM_001164619.1:c.176-20_176-19insC	NP_001158091.1:n.176-20_176-19insC
NM_004484.3:c.338-20_338-19insC , LRG_505t1:c.338-20_338-19insC	NP_004475.1:n.338-20_338-19insC
XM_017029413.2:c.338-20_338-19insC	XP_016884902.1:n.338-20_338-19insC
NM_001164617.2:c.338-20_338-19insC	NP_001158089.1:n.338-20_338-19insC
NM_001164618.2:c.290-20_290-19insC	NP_001158090.1:n.290-20_290-19insC
NM_001164619.2:c.176-20_176-19insC	NP_001158091.1:n.176-20_176-19insC
NM_004484.4:c.338-20_338-19insC MANE Select	NP_004475.1:n.338-20_338-19insC