Canonical Allele Identifier: CA367398712
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 982610
dbSNP Id: rs2096271537

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145596C>T , CM000669.2:g.44145596C>T GRCh38
NC_000007.13:g.44185195C>T , CM000669.1:g.44185195C>T GRCh37
NC_000007.12:g.44151720C>T NCBI36
NG_008847.1:g.48828G>A
NG_008847.2:g.57575G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1152G>A ENSP00000379142.4:n.*1152G>A
ENST00000616242.5:c.*274G>A ENSP00000482149.2:n.*274G>A
ENST00000683378.1:n.380G>A
ENST00000336642.9:c.188G>A ENSP00000338009.5:p.Gly63Glu
ENST00000345378.7:c.1157G>A ENSP00000223366.2:p.Gly386Glu
ENST00000403799.8:c.1154G>A MANE Select ENSP00000384247.3:p.Gly385Glu
ENST00000671824.1:c.1217G>A ENSP00000500264.1:p.Gly406Glu
ENST00000672743.1:n.166G>A
ENST00000673284.1:c.1154G>A ENSP00000499852.1:p.Gly385Glu
ENST00000336642.8:c.206G>A ENSP00000338009.4:p.Gly69Glu
ENST00000345378.6:c.1157G>A ENSP00000223366.2:p.Gly386Glu
ENST00000395796.7:c.1151G>A ENSP00000379142.3:p.Gly384Glu
ENST00000403799.7:c.1154G>A ENSP00000384247.3:p.Gly385Glu
ENST00000437084.1:c.1103G>A ENSP00000402840.1:p.Gly368Glu
ENST00000459642.1:n.534G>A
ENST00000616242.4:c.1151G>A ENSP00000482149.1:p.Gly384Glu
NM_000162.3:c.1154G>A NP_000153.1:p.Gly385Glu
NM_033507.1:c.1157G>A NP_277042.1:p.Gly386Glu
NM_033508.1:c.1151G>A NP_277043.1:p.Gly384Glu
NM_000162.4:c.1154G>A NP_000153.1:p.Gly385Glu
NM_001354800.1:c.1154G>A NP_001341729.1:p.Gly385Glu
NM_001354801.1:c.143G>A NP_001341730.1:p.Gly48Glu
NM_001354802.1:c.14G>A NP_001341731.1:p.Gly5Glu
NM_001354803.1:c.188G>A NP_001341732.1:p.Gly63Glu
NM_033507.2:c.1157G>A NP_277042.1:p.Gly386Glu
NM_033508.2:c.1151G>A NP_277043.1:p.Gly384Glu
XM_024446707.1:c.14G>A XP_024302475.1:p.Gly5Glu
NM_000162.5:c.1154G>A MANE Select NP_000153.1:p.Gly385Glu
NM_033507.3:c.1157G>A NP_277042.1:p.Gly386Glu
NM_033508.3:c.1151G>A NP_277043.1:p.Gly384Glu
NM_001354803.2:c.188G>A NP_001341732.1:p.Gly63Glu