Canonical Allele Identifier: CA367399322
Gene: GCK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145711G>C , CM000669.2:g.44145711G>C GRCh38
NC_000007.13:g.44185310G>C , CM000669.1:g.44185310G>C GRCh37
NC_000007.12:g.44151835G>C NCBI36
NG_008847.1:g.48713C>G
NG_008847.2:g.57460C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1037C>G ENSP00000379142.4:n.*1037C>G
ENST00000616242.5:c.*159C>G ENSP00000482149.2:n.*159C>G
ENST00000683378.1:n.265C>G
ENST00000336642.9:c.73C>G ENSP00000338009.5:p.Gln25Glu
ENST00000345378.7:c.1042C>G ENSP00000223366.2:p.Gln348Glu
ENST00000403799.8:c.1039C>G MANE Select ENSP00000384247.3:p.Gln347Glu
ENST00000671824.1:c.1102C>G ENSP00000500264.1:p.Gln368Glu
ENST00000672743.1:n.51C>G
ENST00000673284.1:c.1039C>G ENSP00000499852.1:p.Gln347Glu
ENST00000336642.8:c.91C>G ENSP00000338009.4:p.Gln31Glu
ENST00000345378.6:c.1042C>G ENSP00000223366.2:p.Gln348Glu
ENST00000395796.7:c.1036C>G ENSP00000379142.3:p.Gln346Glu
ENST00000403799.7:c.1039C>G ENSP00000384247.3:p.Gln347Glu
ENST00000437084.1:c.988C>G ENSP00000402840.1:p.Gln330Glu
ENST00000459642.1:n.419C>G
ENST00000473353.1:n.337C>G
ENST00000616242.4:c.1036C>G ENSP00000482149.1:p.Gln346Glu
NM_000162.3:c.1039C>G NP_000153.1:p.Gln347Glu
NM_033507.1:c.1042C>G NP_277042.1:p.Gln348Glu
NM_033508.1:c.1036C>G NP_277043.1:p.Gln346Glu
NM_000162.4:c.1039C>G NP_000153.1:p.Gln347Glu
NM_001354800.1:c.1039C>G NP_001341729.1:p.Gln347Glu
NM_001354801.1:c.28C>G NP_001341730.1:p.Gln10Glu
NM_001354802.1:c.-102C>G NP_001341731.1:n.-102C>G
NM_001354803.1:c.73C>G NP_001341732.1:p.Gln25Glu
NM_033507.2:c.1042C>G NP_277042.1:p.Gln348Glu
NM_033508.2:c.1036C>G NP_277043.1:p.Gln346Glu
XM_024446707.1:c.-102C>G XP_024302475.1:n.-102C>G
NM_000162.5:c.1039C>G MANE Select NP_000153.1:p.Gln347Glu
NM_033507.3:c.1042C>G NP_277042.1:p.Gln348Glu
NM_033508.3:c.1036C>G NP_277043.1:p.Gln346Glu
NM_001354803.2:c.73C>G NP_001341732.1:p.Gln25Glu