Canonical Allele Identifier: CA367396790
Gene: GCK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145155G>C , CM000669.2:g.44145155G>C GRCh38
NC_000007.13:g.44184754G>C , CM000669.1:g.44184754G>C GRCh37
NC_000007.12:g.44151279G>C NCBI36
NG_008847.1:g.49269C>G
NG_008847.2:g.58016C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1377C>G ENSP00000379142.4:n.*1377C>G
ENST00000616242.5:c.*499C>G ENSP00000482149.2:n.*499C>G
ENST00000683378.1:n.605C>G
ENST00000336642.9:c.413C>G ENSP00000338009.5:p.Ala138Gly
ENST00000345378.7:c.1382C>G ENSP00000223366.2:p.Ala461Gly
ENST00000403799.8:c.1379C>G MANE Select ENSP00000384247.3:p.Ala460Gly
ENST00000671824.1:c.1442C>G ENSP00000500264.1:p.Ala481Gly
ENST00000672743.1:n.381+10C>G
ENST00000673284.1:c.1369+10C>G ENSP00000499852.1:n.1369+10C>G
ENST00000336642.8:c.431C>G ENSP00000338009.4:p.Ala144Gly
ENST00000345378.6:c.1382C>G ENSP00000223366.2:p.Ala461Gly
ENST00000395796.7:c.1376C>G ENSP00000379142.3:p.Ala459Gly
ENST00000403799.7:c.1379C>G ENSP00000384247.3:p.Ala460Gly
ENST00000437084.1:c.1328C>G ENSP00000402840.1:p.Ala443Gly
ENST00000459642.1:n.759C>G
ENST00000616242.4:c.1376C>G ENSP00000482149.1:p.Ala459Gly
NM_000162.3:c.1379C>G NP_000153.1:p.Ala460Gly
NM_033507.1:c.1382C>G NP_277042.1:p.Ala461Gly
NM_033508.1:c.1376C>G NP_277043.1:p.Ala459Gly
NM_000162.4:c.1379C>G NP_000153.1:p.Ala460Gly
NM_001354800.1:c.1369+10C>G NP_001341729.1:n.1369+10C>G
NM_001354801.1:c.368C>G NP_001341730.1:p.Ala123Gly
NM_001354802.1:c.229+10C>G NP_001341731.1:n.229+10C>G
NM_001354803.1:c.413C>G NP_001341732.1:p.Ala138Gly
NM_033507.2:c.1382C>G NP_277042.1:p.Ala461Gly
NM_033508.2:c.1376C>G NP_277043.1:p.Ala459Gly
XM_024446707.1:c.239C>G XP_024302475.1:p.Ala80Gly
NM_000162.5:c.1379C>G MANE Select NP_000153.1:p.Ala460Gly
NM_033507.3:c.1382C>G NP_277042.1:p.Ala461Gly
NM_033508.3:c.1376C>G NP_277043.1:p.Ala459Gly
NM_001354803.2:c.413C>G NP_001341732.1:p.Ala138Gly