Canonical Allele Identifier: CA2694731786

Gene: GPC3

Linked Data

• gnomAD v4: X-133536083-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133536083C>A , CM000685.2:g.133536083C>A	GRCh38
NC_000023.10:g.132670111C>A , CM000685.1:g.132670111C>A	GRCh37
NC_000023.9:g.132497777C>A	NCBI36
NG_009286.1:g.454556G>T , LRG_505:g.454556G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689310.1:c.*41G>T	ENSP00000510438.1:n.*41G>T
ENST00000370818.8:c.*41G>T MANE Select	ENSP00000359854.3:n.*41G>T
ENST00000394299.7:c.*41G>T	ENSP00000377836.2:n.*41G>T
ENST00000669691.1:n.850G>T
ENST00000370818.7:c.*41G>T	ENSP00000359854.3:n.*41G>T
ENST00000394299.6:c.*41G>T	ENSP00000377836.2:n.*41G>T
NM_001164617.1:c.*41G>T	NP_001158089.1:n.*41G>T
NM_001164618.1:c.*41G>T	NP_001158090.1:n.*41G>T
NM_001164619.1:c.*41G>T	NP_001158091.1:n.*41G>T
NM_004484.3:c.*41G>T , LRG_505t1:c.*41G>T	NP_004475.1:n.*41G>T
NM_001164617.2:c.*41G>T	NP_001158089.1:n.*41G>T
NM_001164618.2:c.*41G>T	NP_001158090.1:n.*41G>T
NM_001164619.2:c.*41G>T	NP_001158091.1:n.*41G>T
NM_004484.4:c.*41G>T MANE Select	NP_004475.1:n.*41G>T