Canonical Allele Identifier: CA414706647
Gene: GPC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.133754082A>T , CM000685.2:g.133754082A>T GRCh38
NC_000023.10:g.132888109A>T , CM000685.1:g.132888109A>T GRCh37
NC_000023.9:g.132715775A>T NCBI36
NG_009286.1:g.236558T>A , LRG_505:g.236558T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684880.1:c.*20T>A ENSP00000510280.1:n.*20T>A
ENST00000689310.1:c.384T>A ENSP00000510438.1:p.Phe128Leu
ENST00000692630.1:n.562T>A
ENST00000370818.8:c.432T>A MANE Select ENSP00000359854.3:p.Phe144Leu
ENST00000394299.7:c.432T>A ENSP00000377836.2:p.Phe144Leu
ENST00000370818.7:c.432T>A ENSP00000359854.3:p.Phe144Leu
ENST00000394299.6:c.432T>A ENSP00000377836.2:p.Phe144Leu
ENST00000631057.2:c.270T>A ENSP00000486325.1:p.Phe90Leu
NM_001164617.1:c.432T>A NP_001158089.1:p.Phe144Leu
NM_001164618.1:c.384T>A NP_001158090.1:p.Phe128Leu
NM_001164619.1:c.270T>A NP_001158091.1:p.Phe90Leu
NM_004484.3:c.432T>A , LRG_505t1:c.432T>A NP_004475.1:p.Phe144Leu
XM_017029413.2:c.432T>A XP_016884902.1:p.Phe144Leu
NM_001164617.2:c.432T>A NP_001158089.1:p.Phe144Leu
NM_001164618.2:c.384T>A NP_001158090.1:p.Phe128Leu
NM_001164619.2:c.270T>A NP_001158091.1:p.Phe90Leu
NM_004484.4:c.432T>A MANE Select NP_004475.1:p.Phe144Leu