Canonical Allele Identifier: CA367396972
Gene: GCK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145201T>C , CM000669.2:g.44145201T>C GRCh38
NC_000007.13:g.44184800T>C , CM000669.1:g.44184800T>C GRCh37
NC_000007.12:g.44151325T>C NCBI36
NG_008847.1:g.49223A>G
NG_008847.2:g.57970A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1331A>G ENSP00000379142.4:n.*1331A>G
ENST00000616242.5:c.*453A>G ENSP00000482149.2:n.*453A>G
ENST00000683378.1:n.559A>G
ENST00000336642.9:c.367A>G ENSP00000338009.5:p.Ser123Gly
ENST00000345378.7:c.1336A>G ENSP00000223366.2:p.Ser446Gly
ENST00000403799.8:c.1333A>G MANE Select ENSP00000384247.3:p.Ser445Gly
ENST00000671824.1:c.1396A>G ENSP00000500264.1:p.Ser466Gly
ENST00000672743.1:n.345A>G
ENST00000673284.1:c.1333A>G ENSP00000499852.1:p.Ser445Gly
ENST00000336642.8:c.385A>G ENSP00000338009.4:p.Ser129Gly
ENST00000345378.6:c.1336A>G ENSP00000223366.2:p.Ser446Gly
ENST00000395796.7:c.1330A>G ENSP00000379142.3:p.Ser444Gly
ENST00000403799.7:c.1333A>G ENSP00000384247.3:p.Ser445Gly
ENST00000437084.1:c.1282A>G ENSP00000402840.1:p.Ser428Gly
ENST00000459642.1:n.713A>G
ENST00000616242.4:c.1330A>G ENSP00000482149.1:p.Ser444Gly
NM_000162.3:c.1333A>G NP_000153.1:p.Ser445Gly
NM_033507.1:c.1336A>G NP_277042.1:p.Ser446Gly
NM_033508.1:c.1330A>G NP_277043.1:p.Ser444Gly
NM_000162.4:c.1333A>G NP_000153.1:p.Ser445Gly
NM_001354800.1:c.1333A>G NP_001341729.1:p.Ser445Gly
NM_001354801.1:c.322A>G NP_001341730.1:p.Ser108Gly
NM_001354802.1:c.193A>G NP_001341731.1:p.Ser65Gly
NM_001354803.1:c.367A>G NP_001341732.1:p.Ser123Gly
NM_033507.2:c.1336A>G NP_277042.1:p.Ser446Gly
NM_033508.2:c.1330A>G NP_277043.1:p.Ser444Gly
XM_024446707.1:c.193A>G XP_024302475.1:p.Ser65Gly
NM_000162.5:c.1333A>G MANE Select NP_000153.1:p.Ser445Gly
NM_033507.3:c.1336A>G NP_277042.1:p.Ser446Gly
NM_033508.3:c.1330A>G NP_277043.1:p.Ser444Gly
NM_001354803.2:c.367A>G NP_001341732.1:p.Ser123Gly