Canonical Allele Identifier: CA367398316
Gene: GCK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145523A>C , CM000669.2:g.44145523A>C GRCh38
NC_000007.13:g.44185122A>C , CM000669.1:g.44185122A>C GRCh37
NC_000007.12:g.44151647A>C NCBI36
NG_008847.1:g.48901T>G
NG_008847.2:g.57648T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1225T>G ENSP00000379142.4:n.*1225T>G
ENST00000616242.5:c.*347T>G ENSP00000482149.2:n.*347T>G
ENST00000683378.1:n.453T>G
ENST00000336642.9:c.261T>G ENSP00000338009.5:p.Asp87Glu
ENST00000345378.7:c.1230T>G ENSP00000223366.2:p.Asp410Glu
ENST00000403799.8:c.1227T>G MANE Select ENSP00000384247.3:p.Asp409Glu
ENST00000671824.1:c.1290T>G ENSP00000500264.1:p.Asp430Glu
ENST00000672743.1:n.239T>G
ENST00000673284.1:c.1227T>G ENSP00000499852.1:p.Asp409Glu
ENST00000336642.8:c.279T>G ENSP00000338009.4:p.Asp93Glu
ENST00000345378.6:c.1230T>G ENSP00000223366.2:p.Asp410Glu
ENST00000395796.7:c.1224T>G ENSP00000379142.3:p.Asp408Glu
ENST00000403799.7:c.1227T>G ENSP00000384247.3:p.Asp409Glu
ENST00000437084.1:c.1176T>G ENSP00000402840.1:p.Asp392Glu
ENST00000459642.1:n.607T>G
ENST00000616242.4:c.1224T>G ENSP00000482149.1:p.Asp408Glu
NM_000162.3:c.1227T>G NP_000153.1:p.Asp409Glu
NM_033507.1:c.1230T>G NP_277042.1:p.Asp410Glu
NM_033508.1:c.1224T>G NP_277043.1:p.Asp408Glu
NM_000162.4:c.1227T>G NP_000153.1:p.Asp409Glu
NM_001354800.1:c.1227T>G NP_001341729.1:p.Asp409Glu
NM_001354801.1:c.216T>G NP_001341730.1:p.Asp72Glu
NM_001354802.1:c.87T>G NP_001341731.1:p.Asp29Glu
NM_001354803.1:c.261T>G NP_001341732.1:p.Asp87Glu
NM_033507.2:c.1230T>G NP_277042.1:p.Asp410Glu
NM_033508.2:c.1224T>G NP_277043.1:p.Asp408Glu
XM_024446707.1:c.87T>G XP_024302475.1:p.Asp29Glu
NM_000162.5:c.1227T>G MANE Select NP_000153.1:p.Asp409Glu
NM_033507.3:c.1230T>G NP_277042.1:p.Asp410Glu
NM_033508.3:c.1224T>G NP_277043.1:p.Asp408Glu
NM_001354803.2:c.261T>G NP_001341732.1:p.Asp87Glu