Canonical Allele Identifier: CA4239376
Gene: GCK HGNC NCBI

Linked Data

dbSNP Id: rs140886210
gnomAD v2: 7-44184804-C-T
gnomAD v4: 7-44145205-C-T
COSMIC: COSM107115

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145205C>T , CM000669.2:g.44145205C>T GRCh38
NC_000007.13:g.44184804C>T , CM000669.1:g.44184804C>T GRCh37
NC_000007.12:g.44151329C>T NCBI36
NG_008847.1:g.49219G>A
NG_008847.2:g.57966G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1327G>A ENSP00000379142.4:n.*1327G>A
ENST00000616242.5:c.*449G>A ENSP00000482149.2:n.*449G>A
ENST00000683378.1:n.555G>A
ENST00000336642.9:c.363G>A ENSP00000338009.5:p.Glu121=
ENST00000345378.7:c.1332G>A ENSP00000223366.2:p.Glu444=
ENST00000403799.8:c.1329G>A MANE Select ENSP00000384247.3:p.Glu443=
ENST00000671824.1:c.1392G>A ENSP00000500264.1:p.Glu464=
ENST00000672743.1:n.341G>A
ENST00000673284.1:c.1329G>A ENSP00000499852.1:p.Glu443=
ENST00000336642.8:c.381G>A ENSP00000338009.4:p.Glu127=
ENST00000345378.6:c.1332G>A ENSP00000223366.2:p.Glu444=
ENST00000395796.7:c.1326G>A ENSP00000379142.3:p.Glu442=
ENST00000403799.7:c.1329G>A ENSP00000384247.3:p.Glu443=
ENST00000437084.1:c.1278G>A ENSP00000402840.1:p.Glu426=
ENST00000459642.1:n.709G>A
ENST00000616242.4:c.1326G>A ENSP00000482149.1:p.Glu442=
NM_000162.3:c.1329G>A NP_000153.1:p.Glu443=
NM_033507.1:c.1332G>A NP_277042.1:p.Glu444=
NM_033508.1:c.1326G>A NP_277043.1:p.Glu442=
NM_000162.4:c.1329G>A NP_000153.1:p.Glu443=
NM_001354800.1:c.1329G>A NP_001341729.1:p.Glu443=
NM_001354801.1:c.318G>A NP_001341730.1:p.Glu106=
NM_001354802.1:c.189G>A NP_001341731.1:p.Glu63=
NM_001354803.1:c.363G>A NP_001341732.1:p.Glu121=
NM_033507.2:c.1332G>A NP_277042.1:p.Glu444=
NM_033508.2:c.1326G>A NP_277043.1:p.Glu442=
XM_024446707.1:c.189G>A XP_024302475.1:p.Glu63=
NM_000162.5:c.1329G>A MANE Select NP_000153.1:p.Glu443=
NM_033507.3:c.1332G>A NP_277042.1:p.Glu444=
NM_033508.3:c.1326G>A NP_277043.1:p.Glu442=
NM_001354803.2:c.363G>A NP_001341732.1:p.Glu121=