Canonical Allele Identifier: CA2695202968
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44151016del , CM000669.2:g.44151016del GRCh38
NC_000007.13:g.44190615del , CM000669.1:g.44190615del GRCh37
NC_000007.12:g.44157140del NCBI36
NG_008847.1:g.43408del
NG_008847.2:g.52155del

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*421del ENSP00000379142.4:n.*421del
ENST00000616242.5:c.423del ENSP00000482149.2:p.His141GlnfsTer14
ENST00000682635.1:n.909del
ENST00000345378.7:c.426del ENSP00000223366.2:p.His142GlnfsTer14
ENST00000403799.8:c.423del MANE Select ENSP00000384247.3:p.His141GlnfsTer14
ENST00000671824.1:c.423del ENSP00000500264.1:p.His141GlnfsTer14
ENST00000673284.1:c.423del ENSP00000499852.1:p.His141GlnfsTer14
ENST00000345378.6:c.426del ENSP00000223366.2:p.His142GlnfsTer14
ENST00000395796.7:c.420del ENSP00000379142.3:p.His140GlnfsTer14
ENST00000403799.7:c.423del ENSP00000384247.3:p.His141GlnfsTer14
ENST00000437084.1:c.372del ENSP00000402840.1:p.His124GlnfsTer14
ENST00000616242.4:c.420del ENSP00000482149.1:p.His140GlnfsTer14
NM_000162.3:c.423del NP_000153.1:p.His141GlnfsTer14
NM_033507.1:c.426del NP_277042.1:p.His142GlnfsTer14
NM_033508.1:c.420del NP_277043.1:p.His140GlnfsTer14
NM_000162.4:c.423del NP_000153.1:p.His141GlnfsTer14
NM_001354800.1:c.423del NP_001341729.1:p.His141GlnfsTer14
NM_033507.2:c.426del NP_277042.1:p.His142GlnfsTer14
NM_033508.2:c.420del NP_277043.1:p.His140GlnfsTer14
NM_000162.5:c.423del MANE Select NP_000153.1:p.His141GlnfsTer14
NM_033507.3:c.426del NP_277042.1:p.His142GlnfsTer14
NM_033508.3:c.420del NP_277043.1:p.His140GlnfsTer14
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