Canonical Allele Identifier: CA645564883
Gene: GCK HGNC NCBI

Linked Data

COSMIC: COSM5734714 COSM5734715 COSM5734716
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44151041_44151042del , CM000669.2:g.44151041_44151042del GRCh38
NC_000007.13:g.44190640_44190641del , CM000669.1:g.44190640_44190641del GRCh37
NC_000007.12:g.44157165_44157166del NCBI36
NG_008847.1:g.43382_43383del
NG_008847.2:g.52129_52130del

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*395_*396del ENSP00000379142.4:n.*395_*396del
ENST00000616242.5:c.397_398del ENSP00000482149.2:p.Phe133ProfsTer28
ENST00000682635.1:n.883_884del
ENST00000345378.7:c.400_401del ENSP00000223366.2:p.Phe134ProfsTer28
ENST00000403799.8:c.397_398del MANE Select ENSP00000384247.3:p.Phe133ProfsTer28
ENST00000671824.1:c.397_398del ENSP00000500264.1:p.Phe133ProfsTer28
ENST00000673284.1:c.397_398del ENSP00000499852.1:p.Phe133ProfsTer28
ENST00000345378.6:c.400_401del ENSP00000223366.2:p.Phe134ProfsTer28
ENST00000395796.7:c.394_395del ENSP00000379142.3:p.Phe132ProfsTer28
ENST00000403799.7:c.397_398del ENSP00000384247.3:p.Phe133ProfsTer28
ENST00000437084.1:c.364-18_364-17del ENSP00000402840.1:n.364-18_364-17del
ENST00000616242.4:c.394_395del ENSP00000482149.1:p.Phe132ProfsTer28
NM_000162.3:c.397_398del NP_000153.1:p.Phe133ProfsTer28
NM_033507.1:c.400_401del NP_277042.1:p.Phe134ProfsTer28
NM_033508.1:c.394_395del NP_277043.1:p.Phe132ProfsTer28
NM_000162.4:c.397_398del NP_000153.1:p.Phe133ProfsTer28
NM_001354800.1:c.397_398del NP_001341729.1:p.Phe133ProfsTer28
NM_033507.2:c.400_401del NP_277042.1:p.Phe134ProfsTer28
NM_033508.2:c.394_395del NP_277043.1:p.Phe132ProfsTer28
NM_000162.5:c.397_398del MANE Select NP_000153.1:p.Phe133ProfsTer28
NM_033507.3:c.400_401del NP_277042.1:p.Phe134ProfsTer28
NM_033508.3:c.394_395del NP_277043.1:p.Phe132ProfsTer28
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