Canonical Allele Identifier: CA414706843
Gene: GPC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.133754170A>T , CM000685.2:g.133754170A>T GRCh38
NC_000023.10:g.132888197A>T , CM000685.1:g.132888197A>T GRCh37
NC_000023.9:g.132715863A>T NCBI36
NG_009286.1:g.236470T>A , LRG_505:g.236470T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684880.1:c.415T>A ENSP00000510280.1:p.Leu139Met
ENST00000689310.1:c.296T>A ENSP00000510438.1:p.Phe99Tyr
ENST00000692630.1:n.474T>A
ENST00000370818.8:c.344T>A MANE Select ENSP00000359854.3:p.Phe115Tyr
ENST00000394299.7:c.344T>A ENSP00000377836.2:p.Phe115Tyr
ENST00000370818.7:c.344T>A ENSP00000359854.3:p.Phe115Tyr
ENST00000394299.6:c.344T>A ENSP00000377836.2:p.Phe115Tyr
ENST00000631057.2:c.182T>A ENSP00000486325.1:p.Phe61Tyr
NM_001164617.1:c.344T>A NP_001158089.1:p.Phe115Tyr
NM_001164618.1:c.296T>A NP_001158090.1:p.Phe99Tyr
NM_001164619.1:c.182T>A NP_001158091.1:p.Phe61Tyr
NM_004484.3:c.344T>A , LRG_505t1:c.344T>A NP_004475.1:p.Phe115Tyr
XM_017029413.2:c.344T>A XP_016884902.1:p.Phe115Tyr
NM_001164617.2:c.344T>A NP_001158089.1:p.Phe115Tyr
NM_001164618.2:c.296T>A NP_001158090.1:p.Phe99Tyr
NM_001164619.2:c.182T>A NP_001158091.1:p.Phe61Tyr
NM_004484.4:c.344T>A MANE Select NP_004475.1:p.Phe115Tyr