Canonical Allele Identifier: CA367399204
Gene: GCK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145690T>G , CM000669.2:g.44145690T>G GRCh38
NC_000007.13:g.44185289T>G , CM000669.1:g.44185289T>G GRCh37
NC_000007.12:g.44151814T>G NCBI36
NG_008847.1:g.48734A>C
NG_008847.2:g.57481A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1058A>C ENSP00000379142.4:n.*1058A>C
ENST00000616242.5:c.*180A>C ENSP00000482149.2:n.*180A>C
ENST00000683378.1:n.286A>C
ENST00000336642.9:c.94A>C ENSP00000338009.5:p.Thr32Pro
ENST00000345378.7:c.1063A>C ENSP00000223366.2:p.Thr355Pro
ENST00000403799.8:c.1060A>C MANE Select ENSP00000384247.3:p.Thr354Pro
ENST00000671824.1:c.1123A>C ENSP00000500264.1:p.Thr375Pro
ENST00000672743.1:n.72A>C
ENST00000673284.1:c.1060A>C ENSP00000499852.1:p.Thr354Pro
ENST00000336642.8:c.112A>C ENSP00000338009.4:p.Thr38Pro
ENST00000345378.6:c.1063A>C ENSP00000223366.2:p.Thr355Pro
ENST00000395796.7:c.1057A>C ENSP00000379142.3:p.Thr353Pro
ENST00000403799.7:c.1060A>C ENSP00000384247.3:p.Thr354Pro
ENST00000437084.1:c.1009A>C ENSP00000402840.1:p.Thr337Pro
ENST00000459642.1:n.440A>C
ENST00000473353.1:n.358A>C
ENST00000616242.4:c.1057A>C ENSP00000482149.1:p.Thr353Pro
NM_000162.3:c.1060A>C NP_000153.1:p.Thr354Pro
NM_033507.1:c.1063A>C NP_277042.1:p.Thr355Pro
NM_033508.1:c.1057A>C NP_277043.1:p.Thr353Pro
NM_000162.4:c.1060A>C NP_000153.1:p.Thr354Pro
NM_001354800.1:c.1060A>C NP_001341729.1:p.Thr354Pro
NM_001354801.1:c.49A>C NP_001341730.1:p.Thr17Pro
NM_001354802.1:c.-81A>C NP_001341731.1:n.-81A>C
NM_001354803.1:c.94A>C NP_001341732.1:p.Thr32Pro
NM_033507.2:c.1063A>C NP_277042.1:p.Thr355Pro
NM_033508.2:c.1057A>C NP_277043.1:p.Thr353Pro
XM_024446707.1:c.-81A>C XP_024302475.1:n.-81A>C
NM_000162.5:c.1060A>C MANE Select NP_000153.1:p.Thr354Pro
NM_033507.3:c.1063A>C NP_277042.1:p.Thr355Pro
NM_033508.3:c.1057A>C NP_277043.1:p.Thr353Pro
NM_001354803.2:c.94A>C NP_001341732.1:p.Thr32Pro