Canonical Allele Identifier: CA367399314
Gene: GCK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145710T>C , CM000669.2:g.44145710T>C GRCh38
NC_000007.13:g.44185309T>C , CM000669.1:g.44185309T>C GRCh37
NC_000007.12:g.44151834T>C NCBI36
NG_008847.1:g.48714A>G
NG_008847.2:g.57461A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1038A>G ENSP00000379142.4:n.*1038A>G
ENST00000616242.5:c.*160A>G ENSP00000482149.2:n.*160A>G
ENST00000683378.1:n.266A>G
ENST00000336642.9:c.74A>G ENSP00000338009.5:p.Gln25Arg
ENST00000345378.7:c.1043A>G ENSP00000223366.2:p.Gln348Arg
ENST00000403799.8:c.1040A>G MANE Select ENSP00000384247.3:p.Gln347Arg
ENST00000671824.1:c.1103A>G ENSP00000500264.1:p.Gln368Arg
ENST00000672743.1:n.52A>G
ENST00000673284.1:c.1040A>G ENSP00000499852.1:p.Gln347Arg
ENST00000336642.8:c.92A>G ENSP00000338009.4:p.Gln31Arg
ENST00000345378.6:c.1043A>G ENSP00000223366.2:p.Gln348Arg
ENST00000395796.7:c.1037A>G ENSP00000379142.3:p.Gln346Arg
ENST00000403799.7:c.1040A>G ENSP00000384247.3:p.Gln347Arg
ENST00000437084.1:c.989A>G ENSP00000402840.1:p.Gln330Arg
ENST00000459642.1:n.420A>G
ENST00000473353.1:n.338A>G
ENST00000616242.4:c.1037A>G ENSP00000482149.1:p.Gln346Arg
NM_000162.3:c.1040A>G NP_000153.1:p.Gln347Arg
NM_033507.1:c.1043A>G NP_277042.1:p.Gln348Arg
NM_033508.1:c.1037A>G NP_277043.1:p.Gln346Arg
NM_000162.4:c.1040A>G NP_000153.1:p.Gln347Arg
NM_001354800.1:c.1040A>G NP_001341729.1:p.Gln347Arg
NM_001354801.1:c.29A>G NP_001341730.1:p.Gln10Arg
NM_001354802.1:c.-101A>G NP_001341731.1:n.-101A>G
NM_001354803.1:c.74A>G NP_001341732.1:p.Gln25Arg
NM_033507.2:c.1043A>G NP_277042.1:p.Gln348Arg
NM_033508.2:c.1037A>G NP_277043.1:p.Gln346Arg
XM_024446707.1:c.-101A>G XP_024302475.1:n.-101A>G
NM_000162.5:c.1040A>G MANE Select NP_000153.1:p.Gln347Arg
NM_033507.3:c.1043A>G NP_277042.1:p.Gln348Arg
NM_033508.3:c.1037A>G NP_277043.1:p.Gln346Arg
NM_001354803.2:c.74A>G NP_001341732.1:p.Gln25Arg