Canonical Allele Identifier: CA1703634948
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147802_44147803delinsCT , CM000669.2:g.44147802_44147803delinsCT GRCh38
NC_000007.13:g.44187401_44187402delinsCT , CM000669.1:g.44187401_44187402delinsCT GRCh37
NC_000007.12:g.44153926_44153927delinsCT NCBI36
NG_008847.1:g.46621_46622delinsAG
NG_008847.2:g.55368_55369delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*708_*709delinsAG ENSP00000379142.4:n.*708_*709delinsAG
ENST00000616242.5:c.710_711delinsAG ENSP00000482149.2:p.Glu237=
ENST00000345378.7:c.713_714delinsAG ENSP00000223366.2:p.Glu238=
ENST00000403799.8:c.710_711delinsAG MANE Select ENSP00000384247.3:p.Glu237=
ENST00000671824.1:c.710_711delinsAG ENSP00000500264.1:p.Glu237=
ENST00000673284.1:c.710_711delinsAG ENSP00000499852.1:p.Glu237=
ENST00000345378.6:c.713_714delinsAG ENSP00000223366.2:p.Glu238=
ENST00000395796.7:c.707_708delinsAG ENSP00000379142.3:p.Glu236=
ENST00000403799.7:c.710_711delinsAG ENSP00000384247.3:p.Glu237=
ENST00000437084.1:c.659_660delinsAG ENSP00000402840.1:p.Glu220=
ENST00000616242.4:c.707_708delinsAG ENSP00000482149.1:p.Glu236=
NM_000162.3:c.710_711delinsAG NP_000153.1:p.Glu237=
NM_033507.1:c.713_714delinsAG NP_277042.1:p.Glu238=
NM_033508.1:c.707_708delinsAG NP_277043.1:p.Glu236=
XR_927223.1:n.82+54_82+55delinsCT
NM_000162.4:c.710_711delinsAG NP_000153.1:p.Glu237=
NM_001354800.1:c.710_711delinsAG NP_001341729.1:p.Glu237=
NM_033507.2:c.713_714delinsAG NP_277042.1:p.Glu238=
NM_033508.2:c.707_708delinsAG NP_277043.1:p.Glu236=
XR_927223.2:n.82+54_82+55delinsCT
NM_000162.5:c.710_711delinsAG MANE Select NP_000153.1:p.Glu237=
NM_033507.3:c.713_714delinsAG NP_277042.1:p.Glu238=
NM_033508.3:c.707_708delinsAG NP_277043.1:p.Glu236=
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