Canonical Allele Identifier: CA1703635854
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44149772_44149773delinsCG , CM000669.2:g.44149772_44149773delinsCG GRCh38
NC_000007.13:g.44189371_44189372delinsCG , CM000669.1:g.44189371_44189372delinsCG GRCh37
NC_000007.12:g.44155896_44155897delinsCG NCBI36
NG_008847.1:g.44651_44652delinsCG
NG_008847.2:g.53398_53399delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*664_*665delinsCG ENSP00000379142.4:n.*664_*665delinsCG
ENST00000616242.5:c.666_667delinsCG ENSP00000482149.2:p.Val222=
ENST00000682635.1:n.1152_1153delinsCG
ENST00000345378.7:c.669_670delinsCG ENSP00000223366.2:p.Val223=
ENST00000403799.8:c.666_667delinsCG MANE Select ENSP00000384247.3:p.Val222=
ENST00000671824.1:c.666_667delinsCG ENSP00000500264.1:p.Val222=
ENST00000673284.1:c.666_667delinsCG ENSP00000499852.1:p.Val222=
ENST00000345378.6:c.669_670delinsCG ENSP00000223366.2:p.Val223=
ENST00000395796.7:c.663_664delinsCG ENSP00000379142.3:p.Val221=
ENST00000403799.7:c.666_667delinsCG ENSP00000384247.3:p.Val222=
ENST00000437084.1:c.615_616delinsCG ENSP00000402840.1:p.Val205=
ENST00000616242.4:c.663_664delinsCG ENSP00000482149.1:p.Val221=
NM_000162.3:c.666_667delinsCG NP_000153.1:p.Val222=
NM_033507.1:c.669_670delinsCG NP_277042.1:p.Val223=
NM_033508.1:c.663_664delinsCG NP_277043.1:p.Val221=
XR_927223.1:n.287_288delinsCG
NM_000162.4:c.666_667delinsCG NP_000153.1:p.Val222=
NM_001354800.1:c.666_667delinsCG NP_001341729.1:p.Val222=
NM_033507.2:c.669_670delinsCG NP_277042.1:p.Val223=
NM_033508.2:c.663_664delinsCG NP_277043.1:p.Val221=
NM_000162.5:c.666_667delinsCG MANE Select NP_000153.1:p.Val222=
NM_033507.3:c.669_670delinsCG NP_277042.1:p.Val223=
NM_033508.3:c.663_664delinsCG NP_277043.1:p.Val221=
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