Canonical Allele Identifier: CA367397091
Gene: GCK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145227A>G , CM000669.2:g.44145227A>G GRCh38
NC_000007.13:g.44184826A>G , CM000669.1:g.44184826A>G GRCh37
NC_000007.12:g.44151351A>G NCBI36
NG_008847.1:g.49197T>C
NG_008847.2:g.57944T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1305T>C ENSP00000379142.4:n.*1305T>C
ENST00000616242.5:c.*427T>C ENSP00000482149.2:n.*427T>C
ENST00000683378.1:n.533T>C
ENST00000336642.9:c.341T>C ENSP00000338009.5:p.Ile114Thr
ENST00000345378.7:c.1310T>C ENSP00000223366.2:p.Ile437Thr
ENST00000403799.8:c.1307T>C MANE Select ENSP00000384247.3:p.Ile436Thr
ENST00000671824.1:c.1370T>C ENSP00000500264.1:p.Ile457Thr
ENST00000672743.1:n.319T>C
ENST00000673284.1:c.1307T>C ENSP00000499852.1:p.Ile436Thr
ENST00000336642.8:c.359T>C ENSP00000338009.4:p.Ile120Thr
ENST00000345378.6:c.1310T>C ENSP00000223366.2:p.Ile437Thr
ENST00000395796.7:c.1304T>C ENSP00000379142.3:p.Ile435Thr
ENST00000403799.7:c.1307T>C ENSP00000384247.3:p.Ile436Thr
ENST00000437084.1:c.1256T>C ENSP00000402840.1:p.Ile419Thr
ENST00000459642.1:n.687T>C
ENST00000616242.4:c.1304T>C ENSP00000482149.1:p.Ile435Thr
NM_000162.3:c.1307T>C NP_000153.1:p.Ile436Thr
NM_033507.1:c.1310T>C NP_277042.1:p.Ile437Thr
NM_033508.1:c.1304T>C NP_277043.1:p.Ile435Thr
NM_000162.4:c.1307T>C NP_000153.1:p.Ile436Thr
NM_001354800.1:c.1307T>C NP_001341729.1:p.Ile436Thr
NM_001354801.1:c.296T>C NP_001341730.1:p.Ile99Thr
NM_001354802.1:c.167T>C NP_001341731.1:p.Ile56Thr
NM_001354803.1:c.341T>C NP_001341732.1:p.Ile114Thr
NM_033507.2:c.1310T>C NP_277042.1:p.Ile437Thr
NM_033508.2:c.1304T>C NP_277043.1:p.Ile435Thr
XM_024446707.1:c.167T>C XP_024302475.1:p.Ile56Thr
NM_000162.5:c.1307T>C MANE Select NP_000153.1:p.Ile436Thr
NM_033507.3:c.1310T>C NP_277042.1:p.Ile437Thr
NM_033508.3:c.1304T>C NP_277043.1:p.Ile435Thr
NM_001354803.2:c.341T>C NP_001341732.1:p.Ile114Thr