Canonical Allele Identifier: CA1703634913
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147738C= , CM000669.2:g.44147738C= GRCh38
NC_000007.13:g.44187337C= , CM000669.1:g.44187337C= GRCh37
NC_000007.12:g.44153862C= NCBI36
NG_008847.1:g.46686G=
NG_008847.2:g.55433G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*773G= ENSP00000379142.4:n.*773G=
ENST00000616242.5:c.775G= ENSP00000482149.2:p.Ala259=
ENST00000345378.7:c.778G= ENSP00000223366.2:p.Ala260=
ENST00000403799.8:c.775G= MANE Select ENSP00000384247.3:p.Ala259=
ENST00000671824.1:c.775G= ENSP00000500264.1:p.Ala259=
ENST00000673284.1:c.775G= ENSP00000499852.1:p.Ala259=
ENST00000345378.6:c.778G= ENSP00000223366.2:p.Ala260=
ENST00000395796.7:c.772G= ENSP00000379142.3:p.Ala258=
ENST00000403799.7:c.775G= ENSP00000384247.3:p.Ala259=
ENST00000437084.1:c.724G= ENSP00000402840.1:p.Ala242=
ENST00000616242.4:c.772G= ENSP00000482149.1:p.Ala258=
NM_000162.3:c.775G= NP_000153.1:p.Ala259=
NM_033507.1:c.778G= NP_277042.1:p.Ala260=
NM_033508.1:c.772G= NP_277043.1:p.Ala258=
XR_927223.1:n.72C=
NM_000162.4:c.775G= NP_000153.1:p.Ala259=
NM_001354800.1:c.775G= NP_001341729.1:p.Ala259=
NM_033507.2:c.778G= NP_277042.1:p.Ala260=
NM_033508.2:c.772G= NP_277043.1:p.Ala258=
XR_927223.2:n.72C=
NM_000162.5:c.775G= MANE Select NP_000153.1:p.Ala259=
NM_033507.3:c.778G= NP_277042.1:p.Ala260=
NM_033508.3:c.772G= NP_277043.1:p.Ala258=
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