Canonical Allele Identifier: CA414706589
Gene: GPC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.133754057A>C , CM000685.2:g.133754057A>C GRCh38
NC_000023.10:g.132888084A>C , CM000685.1:g.132888084A>C GRCh37
NC_000023.9:g.132715750A>C NCBI36
NG_009286.1:g.236583T>G , LRG_505:g.236583T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000684880.1:c.*45T>G ENSP00000510280.1:n.*45T>G
ENST00000689310.1:c.409T>G ENSP00000510438.1:p.Ser137Ala
ENST00000692630.1:n.587T>G
ENST00000370818.8:c.457T>G MANE Select ENSP00000359854.3:p.Ser153Ala
ENST00000394299.7:c.457T>G ENSP00000377836.2:p.Ser153Ala
ENST00000370818.7:c.457T>G ENSP00000359854.3:p.Ser153Ala
ENST00000394299.6:c.457T>G ENSP00000377836.2:p.Ser153Ala
ENST00000631057.2:c.295T>G ENSP00000486325.1:p.Ser99Ala
NM_001164617.1:c.457T>G NP_001158089.1:p.Ser153Ala
NM_001164618.1:c.409T>G NP_001158090.1:p.Ser137Ala
NM_001164619.1:c.295T>G NP_001158091.1:p.Ser99Ala
NM_004484.3:c.457T>G , LRG_505t1:c.457T>G NP_004475.1:p.Ser153Ala
XM_017029413.2:c.457T>G XP_016884902.1:p.Ser153Ala
NM_001164617.2:c.457T>G NP_001158089.1:p.Ser153Ala
NM_001164618.2:c.409T>G NP_001158090.1:p.Ser137Ala
NM_001164619.2:c.295T>G NP_001158091.1:p.Ser99Ala
NM_004484.4:c.457T>G MANE Select NP_004475.1:p.Ser153Ala