Canonical Allele Identifier: CA367399102
Gene: GCK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145669T>C , CM000669.2:g.44145669T>C GRCh38
NC_000007.13:g.44185268T>C , CM000669.1:g.44185268T>C GRCh37
NC_000007.12:g.44151793T>C NCBI36
NG_008847.1:g.48755A>G
NG_008847.2:g.57502A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1079A>G ENSP00000379142.4:n.*1079A>G
ENST00000616242.5:c.*201A>G ENSP00000482149.2:n.*201A>G
ENST00000683378.1:n.307A>G
ENST00000336642.9:c.115A>G ENSP00000338009.5:p.Thr39Ala
ENST00000345378.7:c.1084A>G ENSP00000223366.2:p.Thr362Ala
ENST00000403799.8:c.1081A>G MANE Select ENSP00000384247.3:p.Thr361Ala
ENST00000671824.1:c.1144A>G ENSP00000500264.1:p.Thr382Ala
ENST00000672743.1:n.93A>G
ENST00000673284.1:c.1081A>G ENSP00000499852.1:p.Thr361Ala
ENST00000336642.8:c.133A>G ENSP00000338009.4:p.Thr45Ala
ENST00000345378.6:c.1084A>G ENSP00000223366.2:p.Thr362Ala
ENST00000395796.7:c.1078A>G ENSP00000379142.3:p.Thr360Ala
ENST00000403799.7:c.1081A>G ENSP00000384247.3:p.Thr361Ala
ENST00000437084.1:c.1030A>G ENSP00000402840.1:p.Thr344Ala
ENST00000459642.1:n.461A>G
ENST00000473353.1:n.379A>G
ENST00000616242.4:c.1078A>G ENSP00000482149.1:p.Thr360Ala
NM_000162.3:c.1081A>G NP_000153.1:p.Thr361Ala
NM_033507.1:c.1084A>G NP_277042.1:p.Thr362Ala
NM_033508.1:c.1078A>G NP_277043.1:p.Thr360Ala
NM_000162.4:c.1081A>G NP_000153.1:p.Thr361Ala
NM_001354800.1:c.1081A>G NP_001341729.1:p.Thr361Ala
NM_001354801.1:c.70A>G NP_001341730.1:p.Thr24Ala
NM_001354802.1:c.-60A>G NP_001341731.1:n.-60A>G
NM_001354803.1:c.115A>G NP_001341732.1:p.Thr39Ala
NM_033507.2:c.1084A>G NP_277042.1:p.Thr362Ala
NM_033508.2:c.1078A>G NP_277043.1:p.Thr360Ala
XM_024446707.1:c.-60A>G XP_024302475.1:n.-60A>G
NM_000162.5:c.1081A>G MANE Select NP_000153.1:p.Thr361Ala
NM_033507.3:c.1084A>G NP_277042.1:p.Thr362Ala
NM_033508.3:c.1078A>G NP_277043.1:p.Thr360Ala
NM_001354803.2:c.115A>G NP_001341732.1:p.Thr39Ala