Canonical Allele Identifier: CA414706555
Gene: GPC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.133754042C>T , CM000685.2:g.133754042C>T GRCh38
NC_000023.10:g.132888069C>T , CM000685.1:g.132888069C>T GRCh37
NC_000023.9:g.132715735C>T NCBI36
NG_009286.1:g.236598G>A , LRG_505:g.236598G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684880.1:c.*60G>A ENSP00000510280.1:n.*60G>A
ENST00000689310.1:c.424G>A ENSP00000510438.1:p.Gly142Ser
ENST00000370818.8:c.472G>A MANE Select ENSP00000359854.3:p.Gly158Ser
ENST00000394299.7:c.472G>A ENSP00000377836.2:p.Gly158Ser
ENST00000370818.7:c.472G>A ENSP00000359854.3:p.Gly158Ser
ENST00000394299.6:c.472G>A ENSP00000377836.2:p.Gly158Ser
ENST00000631057.2:c.310G>A ENSP00000486325.1:p.Gly104Ser
NM_001164617.1:c.472G>A NP_001158089.1:p.Gly158Ser
NM_001164618.1:c.424G>A NP_001158090.1:p.Gly142Ser
NM_001164619.1:c.310G>A NP_001158091.1:p.Gly104Ser
NM_004484.3:c.472G>A , LRG_505t1:c.472G>A NP_004475.1:p.Gly158Ser
XM_017029413.2:c.472G>A XP_016884902.1:p.Gly158Ser
NM_001164617.2:c.472G>A NP_001158089.1:p.Gly158Ser
NM_001164618.2:c.424G>A NP_001158090.1:p.Gly142Ser
NM_001164619.2:c.310G>A NP_001158091.1:p.Gly104Ser
NM_004484.4:c.472G>A MANE Select NP_004475.1:p.Gly158Ser