Canonical Allele Identifier: CA2579705510

Gene: GPC3

Linked Data

• gnomAD v4: X-133536111-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133536111G>T , CM000685.2:g.133536111G>T	GRCh38
NC_000023.10:g.132670139G>T , CM000685.1:g.132670139G>T	GRCh37
NC_000023.9:g.132497805G>T	NCBI36
NG_009286.1:g.454528C>A , LRG_505:g.454528C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689310.1:c.*13C>A	ENSP00000510438.1:n.*13C>A
ENST00000370818.8:c.*13C>A MANE Select	ENSP00000359854.3:n.*13C>A
ENST00000394299.7:c.*13C>A	ENSP00000377836.2:n.*13C>A
ENST00000669691.1:n.822C>A
ENST00000370818.7:c.*13C>A	ENSP00000359854.3:n.*13C>A
ENST00000394299.6:c.*13C>A	ENSP00000377836.2:n.*13C>A
NM_001164617.1:c.*13C>A	NP_001158089.1:n.*13C>A
NM_001164618.1:c.*13C>A	NP_001158090.1:n.*13C>A
NM_001164619.1:c.*13C>A	NP_001158091.1:n.*13C>A
NM_004484.3:c.*13C>A , LRG_505t1:c.*13C>A	NP_004475.1:n.*13C>A
NM_001164617.2:c.*13C>A	NP_001158089.1:n.*13C>A
NM_001164618.2:c.*13C>A	NP_001158090.1:n.*13C>A
NM_001164619.2:c.*13C>A	NP_001158091.1:n.*13C>A
NM_004484.4:c.*13C>A MANE Select	NP_004475.1:n.*13C>A