Canonical Allele Identifier: CA367398495
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2136507
ClinVar RCV Id: RCV003060098
gnomAD v4: 7-44145555-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145555C>A , CM000669.2:g.44145555C>A GRCh38
NC_000007.13:g.44185154C>A , CM000669.1:g.44185154C>A GRCh37
NC_000007.12:g.44151679C>A NCBI36
NG_008847.1:g.48869G>T
NG_008847.2:g.57616G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1193G>T ENSP00000379142.4:n.*1193G>T
ENST00000616242.5:c.*315G>T ENSP00000482149.2:n.*315G>T
ENST00000683378.1:n.421G>T
ENST00000336642.9:c.229G>T ENSP00000338009.5:p.Glu77Ter
ENST00000345378.7:c.1198G>T ENSP00000223366.2:p.Glu400Ter
ENST00000403799.8:c.1195G>T MANE Select ENSP00000384247.3:p.Glu399Ter
ENST00000671824.1:c.1258G>T ENSP00000500264.1:p.Glu420Ter
ENST00000672743.1:n.207G>T
ENST00000673284.1:c.1195G>T ENSP00000499852.1:p.Glu399Ter
ENST00000336642.8:c.247G>T ENSP00000338009.4:p.Glu83Ter
ENST00000345378.6:c.1198G>T ENSP00000223366.2:p.Glu400Ter
ENST00000395796.7:c.1192G>T ENSP00000379142.3:p.Glu398Ter
ENST00000403799.7:c.1195G>T ENSP00000384247.3:p.Glu399Ter
ENST00000437084.1:c.1144G>T ENSP00000402840.1:p.Glu382Ter
ENST00000459642.1:n.575G>T
ENST00000616242.4:c.1192G>T ENSP00000482149.1:p.Glu398Ter
NM_000162.3:c.1195G>T NP_000153.1:p.Glu399Ter
NM_033507.1:c.1198G>T NP_277042.1:p.Glu400Ter
NM_033508.1:c.1192G>T NP_277043.1:p.Glu398Ter
NM_000162.4:c.1195G>T NP_000153.1:p.Glu399Ter
NM_001354800.1:c.1195G>T NP_001341729.1:p.Glu399Ter
NM_001354801.1:c.184G>T NP_001341730.1:p.Glu62Ter
NM_001354802.1:c.55G>T NP_001341731.1:p.Glu19Ter
NM_001354803.1:c.229G>T NP_001341732.1:p.Glu77Ter
NM_033507.2:c.1198G>T NP_277042.1:p.Glu400Ter
NM_033508.2:c.1192G>T NP_277043.1:p.Glu398Ter
XM_024446707.1:c.55G>T XP_024302475.1:p.Glu19Ter
NM_000162.5:c.1195G>T MANE Select NP_000153.1:p.Glu399Ter
NM_033507.3:c.1198G>T NP_277042.1:p.Glu400Ter
NM_033508.3:c.1192G>T NP_277043.1:p.Glu398Ter
NM_001354803.2:c.229G>T NP_001341732.1:p.Glu77Ter