Canonical Allele Identifier: CA1703637523
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44153330G= , CM000669.2:g.44153330G= GRCh38
NC_000007.13:g.44192929G= , CM000669.1:g.44192929G= GRCh37
NC_000007.12:g.44159454G= NCBI36
NG_008847.1:g.41094C=
NG_008847.2:g.49841C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*177C= ENSP00000379142.4:n.*177C=
ENST00000616242.5:c.179C= ENSP00000482149.2:p.Thr60=
ENST00000682635.1:n.665C=
ENST00000345378.7:c.182C= ENSP00000223366.2:p.Thr61=
ENST00000403799.8:c.179C= MANE Select ENSP00000384247.3:p.Thr60=
ENST00000671824.1:c.179C= ENSP00000500264.1:p.Thr60=
ENST00000673284.1:c.179C= ENSP00000499852.1:p.Thr60=
ENST00000345378.6:c.182C= ENSP00000223366.2:p.Thr61=
ENST00000395796.7:c.176C= ENSP00000379142.3:p.Thr59=
ENST00000403799.7:c.179C= ENSP00000384247.3:p.Thr60=
ENST00000437084.1:c.179C= ENSP00000402840.1:p.Thr60=
ENST00000616242.4:c.176C= ENSP00000482149.1:p.Thr59=
NM_000162.3:c.179C= NP_000153.1:p.Thr60=
NM_033507.1:c.182C= NP_277042.1:p.Thr61=
NM_033508.1:c.176C= NP_277043.1:p.Thr59=
NM_000162.4:c.179C= NP_000153.1:p.Thr60=
NM_001354800.1:c.179C= NP_001341729.1:p.Thr60=
NM_033507.2:c.182C= NP_277042.1:p.Thr61=
NM_033508.2:c.176C= NP_277043.1:p.Thr59=
NM_000162.5:c.179C= MANE Select NP_000153.1:p.Thr60=
NM_033507.3:c.182C= NP_277042.1:p.Thr61=
NM_033508.3:c.176C= NP_277043.1:p.Thr59=
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