Canonical Allele Identifier: CA414706612
Gene: GPC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.133754068A>C , CM000685.2:g.133754068A>C GRCh38
NC_000023.10:g.132888095A>C , CM000685.1:g.132888095A>C GRCh37
NC_000023.9:g.132715761A>C NCBI36
NG_009286.1:g.236572T>G , LRG_505:g.236572T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000684880.1:c.*34T>G ENSP00000510280.1:n.*34T>G
ENST00000689310.1:c.398T>G ENSP00000510438.1:p.Phe133Cys
ENST00000692630.1:n.576T>G
ENST00000370818.8:c.446T>G MANE Select ENSP00000359854.3:p.Phe149Cys
ENST00000394299.7:c.446T>G ENSP00000377836.2:p.Phe149Cys
ENST00000370818.7:c.446T>G ENSP00000359854.3:p.Phe149Cys
ENST00000394299.6:c.446T>G ENSP00000377836.2:p.Phe149Cys
ENST00000631057.2:c.284T>G ENSP00000486325.1:p.Phe95Cys
NM_001164617.1:c.446T>G NP_001158089.1:p.Phe149Cys
NM_001164618.1:c.398T>G NP_001158090.1:p.Phe133Cys
NM_001164619.1:c.284T>G NP_001158091.1:p.Phe95Cys
NM_004484.3:c.446T>G , LRG_505t1:c.446T>G NP_004475.1:p.Phe149Cys
XM_017029413.2:c.446T>G XP_016884902.1:p.Phe149Cys
NM_001164617.2:c.446T>G NP_001158089.1:p.Phe149Cys
NM_001164618.2:c.398T>G NP_001158090.1:p.Phe133Cys
NM_001164619.2:c.284T>G NP_001158091.1:p.Phe95Cys
NM_004484.4:c.446T>G MANE Select NP_004475.1:p.Phe149Cys