Canonical Allele Identifier: CA2838724733
Gene: GPC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.133754072del , CM000685.2:g.133754072del GRCh38
NC_000023.10:g.132888099del , CM000685.1:g.132888099del GRCh37
NC_000023.9:g.132715765del NCBI36
NG_009286.1:g.236572del , LRG_505:g.236572del

Transcript Alleles

HGVS Amino-acid Change
ENST00000684880.1:c.*34del ENSP00000510280.1:n.*34del
ENST00000689310.1:c.398del ENSP00000510438.1:p.Phe133SerfsTer15
ENST00000692630.1:n.576del
ENST00000370818.8:c.446del MANE Select ENSP00000359854.3:p.Phe149SerfsTer15
ENST00000394299.7:c.446del ENSP00000377836.2:p.Phe149SerfsTer15
ENST00000370818.7:c.446del ENSP00000359854.3:p.Phe149SerfsTer15
ENST00000394299.6:c.446del ENSP00000377836.2:p.Phe149SerfsTer15
ENST00000631057.2:c.284del ENSP00000486325.1:p.Phe95SerfsTer15
NM_001164617.1:c.446del NP_001158089.1:p.Phe149SerfsTer15
NM_001164618.1:c.398del NP_001158090.1:p.Phe133SerfsTer15
NM_001164619.1:c.284del NP_001158091.1:p.Phe95SerfsTer15
NM_004484.3:c.446del , LRG_505t1:c.446del NP_004475.1:p.Phe149SerfsTer15
XM_017029413.2:c.446del XP_016884902.1:p.Phe149SerfsTer15
NM_001164617.2:c.446del NP_001158089.1:p.Phe149SerfsTer15
NM_001164618.2:c.398del NP_001158090.1:p.Phe133SerfsTer15
NM_001164619.2:c.284del NP_001158091.1:p.Phe95SerfsTer15
NM_004484.4:c.446del MANE Select NP_004475.1:p.Phe149SerfsTer15