Canonical Allele Identifier: CA644535830

Gene: GPC3

Linked Data

• dbSNP Id: rs1434813051
• gnomAD v2: X-132670120-G-A
• gnomAD v4: X-133536092-G-A
• MyVariant Identifiers: chrX:g.132670120G>A (hg19) ; chrX:g.133536092G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133536092G>A , CM000685.2:g.133536092G>A	GRCh38
NC_000023.10:g.132670120G>A , CM000685.1:g.132670120G>A	GRCh37
NC_000023.9:g.132497786G>A	NCBI36
NG_009286.1:g.454547C>T , LRG_505:g.454547C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689310.1:c.*32C>T	ENSP00000510438.1:n.*32C>T
ENST00000370818.8:c.*32C>T MANE Select	ENSP00000359854.3:n.*32C>T
ENST00000394299.7:c.*32C>T	ENSP00000377836.2:n.*32C>T
ENST00000669691.1:n.841C>T
ENST00000370818.7:c.*32C>T	ENSP00000359854.3:n.*32C>T
ENST00000394299.6:c.*32C>T	ENSP00000377836.2:n.*32C>T
NM_001164617.1:c.*32C>T	NP_001158089.1:n.*32C>T
NM_001164618.1:c.*32C>T	NP_001158090.1:n.*32C>T
NM_001164619.1:c.*32C>T	NP_001158091.1:n.*32C>T
NM_004484.3:c.*32C>T , LRG_505t1:c.*32C>T	NP_004475.1:n.*32C>T
NM_001164617.2:c.*32C>T	NP_001158089.1:n.*32C>T
NM_001164618.2:c.*32C>T	NP_001158090.1:n.*32C>T
NM_001164619.2:c.*32C>T	NP_001158091.1:n.*32C>T
NM_004484.4:c.*32C>T MANE Select	NP_004475.1:n.*32C>T