Canonical Allele Identifier: CA10588428
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 265174
ClinVar RCV Id: RCV000256137 RCV001844105
dbSNP Id: rs886039380
COSMIC: COSM239959
MyVariant Identifiers: chr7:g.44189614C>T (hg19) chr7:g.44150015C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44150015C>T , CM000669.2:g.44150015C>T GRCh38
NC_000007.13:g.44189614C>T , CM000669.1:g.44189614C>T GRCh37
NC_000007.12:g.44156139C>T NCBI36
NG_008847.1:g.44409G>A
NG_008847.2:g.53156G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*531G>A ENSP00000379142.4:n.*531G>A
ENST00000616242.5:c.533G>A ENSP00000482149.2:p.Gly178Glu
ENST00000682635.1:n.1019G>A
ENST00000345378.7:c.536G>A ENSP00000223366.2:p.Gly179Glu
ENST00000403799.8:c.533G>A MANE Select ENSP00000384247.3:p.Gly178Glu
ENST00000671824.1:c.533G>A ENSP00000500264.1:p.Gly178Glu
ENST00000673284.1:c.533G>A ENSP00000499852.1:p.Gly178Glu
ENST00000345378.6:c.536G>A ENSP00000223366.2:p.Gly179Glu
ENST00000395796.7:c.530G>A ENSP00000379142.3:p.Gly177Glu
ENST00000403799.7:c.533G>A ENSP00000384247.3:p.Gly178Glu
ENST00000437084.1:c.482G>A ENSP00000402840.1:p.Gly161Glu
ENST00000616242.4:c.530G>A ENSP00000482149.1:p.Gly177Glu
NM_000162.3:c.533G>A NP_000153.1:p.Gly178Glu
NM_033507.1:c.536G>A NP_277042.1:p.Gly179Glu
NM_033508.1:c.530G>A NP_277043.1:p.Gly177Glu
NM_000162.4:c.533G>A NP_000153.1:p.Gly178Glu
NM_001354800.1:c.533G>A NP_001341729.1:p.Gly178Glu
NM_033507.2:c.536G>A NP_277042.1:p.Gly179Glu
NM_033508.2:c.530G>A NP_277043.1:p.Gly177Glu
NM_000162.5:c.533G>A MANE Select NP_000153.1:p.Gly178Glu
NM_033507.3:c.536G>A NP_277042.1:p.Gly179Glu
NM_033508.3:c.530G>A NP_277043.1:p.Gly177Glu
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