Canonical Allele Identifier: CA335966662

Gene: GPC3

Linked Data

• dbSNP Id: rs980436939
• gnomAD v4: X-133536104-A-T
• MyVariant Identifiers: chrX:g.132670132A>T (hg19) ; chrX:g.133536104A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133536104A>T , CM000685.2:g.133536104A>T	GRCh38
NC_000023.10:g.132670132A>T , CM000685.1:g.132670132A>T	GRCh37
NC_000023.9:g.132497798A>T	NCBI36
NG_009286.1:g.454535T>A , LRG_505:g.454535T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689310.1:c.*20T>A	ENSP00000510438.1:n.*20T>A
ENST00000370818.8:c.*20T>A MANE Select	ENSP00000359854.3:n.*20T>A
ENST00000394299.7:c.*20T>A	ENSP00000377836.2:n.*20T>A
ENST00000669691.1:n.829T>A
ENST00000370818.7:c.*20T>A	ENSP00000359854.3:n.*20T>A
ENST00000394299.6:c.*20T>A	ENSP00000377836.2:n.*20T>A
NM_001164617.1:c.*20T>A	NP_001158089.1:n.*20T>A
NM_001164618.1:c.*20T>A	NP_001158090.1:n.*20T>A
NM_001164619.1:c.*20T>A	NP_001158091.1:n.*20T>A
NM_004484.3:c.*20T>A , LRG_505t1:c.*20T>A	NP_004475.1:n.*20T>A
NM_001164617.2:c.*20T>A	NP_001158089.1:n.*20T>A
NM_001164618.2:c.*20T>A	NP_001158090.1:n.*20T>A
NM_001164619.2:c.*20T>A	NP_001158091.1:n.*20T>A
NM_004484.4:c.*20T>A MANE Select	NP_004475.1:n.*20T>A