Canonical Allele Identifier: CA2459438262
Gene: GPC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.133536117C= , CM000685.2:g.133536117C= GRCh38
NC_000023.10:g.132670145C= , CM000685.1:g.132670145C= GRCh37
NC_000023.9:g.132497811C= NCBI36
NG_009286.1:g.454522G= , LRG_505:g.454522G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000689310.1:c.*7G= ENSP00000510438.1:n.*7G=
ENST00000370818.8:c.*7G= MANE Select ENSP00000359854.3:n.*7G=
ENST00000394299.7:c.*7G= ENSP00000377836.2:n.*7G=
ENST00000669691.1:n.816G=
ENST00000370818.7:c.*7G= ENSP00000359854.3:n.*7G=
ENST00000394299.6:c.*7G= ENSP00000377836.2:n.*7G=
NM_001164617.1:c.*7G= NP_001158089.1:n.*7G=
NM_001164618.1:c.*7G= NP_001158090.1:n.*7G=
NM_001164619.1:c.*7G= NP_001158091.1:n.*7G=
NM_004484.3:c.*7G= , LRG_505t1:c.*7G= NP_004475.1:n.*7G=
NM_001164617.2:c.*7G= NP_001158089.1:n.*7G=
NM_001164618.2:c.*7G= NP_001158090.1:n.*7G=
NM_001164619.2:c.*7G= NP_001158091.1:n.*7G=
NM_004484.4:c.*7G= MANE Select NP_004475.1:n.*7G=