Canonical Allele Identifier: CA2694731740
Gene: GPC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.133536032_133536033insC , CM000685.2:g.133536032_133536033insC GRCh38
NC_000023.10:g.132670060_132670061insC , CM000685.1:g.132670060_132670061insC GRCh37
NC_000023.9:g.132497726_132497727insC NCBI36
NG_009286.1:g.454606_454607insG , LRG_505:g.454606_454607insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000689310.1:c.*91_*92insG ENSP00000510438.1:n.*91_*92insG
ENST00000370818.8:c.*91_*92insG MANE Select ENSP00000359854.3:n.*91_*92insG
ENST00000394299.7:c.*91_*92insG ENSP00000377836.2:n.*91_*92insG
ENST00000669691.1:n.900_901insG
ENST00000370818.7:c.*91_*92insG ENSP00000359854.3:n.*91_*92insG
ENST00000394299.6:c.*91_*92insG ENSP00000377836.2:n.*91_*92insG
NM_001164617.1:c.*91_*92insG NP_001158089.1:n.*91_*92insG
NM_001164618.1:c.*91_*92insG NP_001158090.1:n.*91_*92insG
NM_001164619.1:c.*91_*92insG NP_001158091.1:n.*91_*92insG
NM_004484.3:c.*91_*92insG , LRG_505t1:c.*91_*92insG NP_004475.1:n.*91_*92insG
NM_001164617.2:c.*91_*92insG NP_001158089.1:n.*91_*92insG
NM_001164618.2:c.*91_*92insG NP_001158090.1:n.*91_*92insG
NM_001164619.2:c.*91_*92insG NP_001158091.1:n.*91_*92insG
NM_004484.4:c.*91_*92insG MANE Select NP_004475.1:n.*91_*92insG