Canonical Allele Identifier: CA2695202965
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2921032
ClinVar RCV Id: RCV003740508
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44151007_44151008delinsAG , CM000669.2:g.44151007_44151008delinsAG GRCh38
NC_000007.13:g.44190606_44190607delinsAG , CM000669.1:g.44190606_44190607delinsAG GRCh37
NC_000007.12:g.44157131_44157132delinsAG NCBI36
NG_008847.1:g.43416_43417delinsCT
NG_008847.2:g.52163_52164delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*429_*430delinsCT ENSP00000379142.4:n.*429_*430delinsCT
ENST00000616242.5:c.431_432delinsCT ENSP00000482149.2:p.Leu144Pro
ENST00000682635.1:n.917_918delinsCT
ENST00000345378.7:c.434_435delinsCT ENSP00000223366.2:p.Leu145Pro
ENST00000403799.8:c.431_432delinsCT MANE Select ENSP00000384247.3:p.Leu144Pro
ENST00000671824.1:c.431_432delinsCT ENSP00000500264.1:p.Leu144Pro
ENST00000673284.1:c.431_432delinsCT ENSP00000499852.1:p.Leu144Pro
ENST00000345378.6:c.434_435delinsCT ENSP00000223366.2:p.Leu145Pro
ENST00000395796.7:c.428_429delinsCT ENSP00000379142.3:p.Leu143Pro
ENST00000403799.7:c.431_432delinsCT ENSP00000384247.3:p.Leu144Pro
ENST00000437084.1:c.380_381delinsCT ENSP00000402840.1:p.Leu127Pro
ENST00000616242.4:c.428_429delinsCT ENSP00000482149.1:p.Leu143Pro
NM_000162.3:c.431_432delinsCT NP_000153.1:p.Leu144Pro
NM_033507.1:c.434_435delinsCT NP_277042.1:p.Leu145Pro
NM_033508.1:c.428_429delinsCT NP_277043.1:p.Leu143Pro
NM_000162.4:c.431_432delinsCT NP_000153.1:p.Leu144Pro
NM_001354800.1:c.431_432delinsCT NP_001341729.1:p.Leu144Pro
NM_033507.2:c.434_435delinsCT NP_277042.1:p.Leu145Pro
NM_033508.2:c.428_429delinsCT NP_277043.1:p.Leu143Pro
NM_000162.5:c.431_432delinsCT MANE Select NP_000153.1:p.Leu144Pro
NM_033507.3:c.434_435delinsCT NP_277042.1:p.Leu145Pro
NM_033508.3:c.428_429delinsCT NP_277043.1:p.Leu143Pro
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