Canonical Allele Identifier: CA367399060
Gene: GCK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145661G>C , CM000669.2:g.44145661G>C GRCh38
NC_000007.13:g.44185260G>C , CM000669.1:g.44185260G>C GRCh37
NC_000007.12:g.44151785G>C NCBI36
NG_008847.1:g.48763C>G
NG_008847.2:g.57510C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1087C>G ENSP00000379142.4:n.*1087C>G
ENST00000616242.5:c.*209C>G ENSP00000482149.2:n.*209C>G
ENST00000683378.1:n.315C>G
ENST00000336642.9:c.123C>G ENSP00000338009.5:p.Asp41Glu
ENST00000345378.7:c.1092C>G ENSP00000223366.2:p.Asp364Glu
ENST00000403799.8:c.1089C>G MANE Select ENSP00000384247.3:p.Asp363Glu
ENST00000671824.1:c.1152C>G ENSP00000500264.1:p.Asp384Glu
ENST00000672743.1:n.101C>G
ENST00000673284.1:c.1089C>G ENSP00000499852.1:p.Asp363Glu
ENST00000336642.8:c.141C>G ENSP00000338009.4:p.Asp47Glu
ENST00000345378.6:c.1092C>G ENSP00000223366.2:p.Asp364Glu
ENST00000395796.7:c.1086C>G ENSP00000379142.3:p.Asp362Glu
ENST00000403799.7:c.1089C>G ENSP00000384247.3:p.Asp363Glu
ENST00000437084.1:c.1038C>G ENSP00000402840.1:p.Asp346Glu
ENST00000459642.1:n.469C>G
ENST00000473353.1:n.387C>G
ENST00000616242.4:c.1086C>G ENSP00000482149.1:p.Asp362Glu
NM_000162.3:c.1089C>G NP_000153.1:p.Asp363Glu
NM_033507.1:c.1092C>G NP_277042.1:p.Asp364Glu
NM_033508.1:c.1086C>G NP_277043.1:p.Asp362Glu
NM_000162.4:c.1089C>G NP_000153.1:p.Asp363Glu
NM_001354800.1:c.1089C>G NP_001341729.1:p.Asp363Glu
NM_001354801.1:c.78C>G NP_001341730.1:p.Asp26Glu
NM_001354802.1:c.-52C>G NP_001341731.1:n.-52C>G
NM_001354803.1:c.123C>G NP_001341732.1:p.Asp41Glu
NM_033507.2:c.1092C>G NP_277042.1:p.Asp364Glu
NM_033508.2:c.1086C>G NP_277043.1:p.Asp362Glu
XM_024446707.1:c.-52C>G XP_024302475.1:n.-52C>G
NM_000162.5:c.1089C>G MANE Select NP_000153.1:p.Asp363Glu
NM_033507.3:c.1092C>G NP_277042.1:p.Asp364Glu
NM_033508.3:c.1086C>G NP_277043.1:p.Asp362Glu
NM_001354803.2:c.123C>G NP_001341732.1:p.Asp41Glu