Canonical Allele Identifier: CA367398377
Gene: GCK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145536G>C , CM000669.2:g.44145536G>C GRCh38
NC_000007.13:g.44185135G>C , CM000669.1:g.44185135G>C GRCh37
NC_000007.12:g.44151660G>C NCBI36
NG_008847.1:g.48888C>G
NG_008847.2:g.57635C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1212C>G ENSP00000379142.4:n.*1212C>G
ENST00000616242.5:c.*334C>G ENSP00000482149.2:n.*334C>G
ENST00000683378.1:n.440C>G
ENST00000336642.9:c.248C>G ENSP00000338009.5:p.Thr83Ser
ENST00000345378.7:c.1217C>G ENSP00000223366.2:p.Thr406Ser
ENST00000403799.8:c.1214C>G MANE Select ENSP00000384247.3:p.Thr405Ser
ENST00000671824.1:c.1277C>G ENSP00000500264.1:p.Thr426Ser
ENST00000672743.1:n.226C>G
ENST00000673284.1:c.1214C>G ENSP00000499852.1:p.Thr405Ser
ENST00000336642.8:c.266C>G ENSP00000338009.4:p.Thr89Ser
ENST00000345378.6:c.1217C>G ENSP00000223366.2:p.Thr406Ser
ENST00000395796.7:c.1211C>G ENSP00000379142.3:p.Thr404Ser
ENST00000403799.7:c.1214C>G ENSP00000384247.3:p.Thr405Ser
ENST00000437084.1:c.1163C>G ENSP00000402840.1:p.Thr388Ser
ENST00000459642.1:n.594C>G
ENST00000616242.4:c.1211C>G ENSP00000482149.1:p.Thr404Ser
NM_000162.3:c.1214C>G NP_000153.1:p.Thr405Ser
NM_033507.1:c.1217C>G NP_277042.1:p.Thr406Ser
NM_033508.1:c.1211C>G NP_277043.1:p.Thr404Ser
NM_000162.4:c.1214C>G NP_000153.1:p.Thr405Ser
NM_001354800.1:c.1214C>G NP_001341729.1:p.Thr405Ser
NM_001354801.1:c.203C>G NP_001341730.1:p.Thr68Ser
NM_001354802.1:c.74C>G NP_001341731.1:p.Thr25Ser
NM_001354803.1:c.248C>G NP_001341732.1:p.Thr83Ser
NM_033507.2:c.1217C>G NP_277042.1:p.Thr406Ser
NM_033508.2:c.1211C>G NP_277043.1:p.Thr404Ser
XM_024446707.1:c.74C>G XP_024302475.1:p.Thr25Ser
NM_000162.5:c.1214C>G MANE Select NP_000153.1:p.Thr405Ser
NM_033507.3:c.1217C>G NP_277042.1:p.Thr406Ser
NM_033508.3:c.1211C>G NP_277043.1:p.Thr404Ser
NM_001354803.2:c.248C>G NP_001341732.1:p.Thr83Ser