Canonical Allele Identifier: CA2775231743
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44153529_44153531del , CM000669.2:g.44153529_44153531del GRCh38
NC_000007.13:g.44193128_44193130del , CM000669.1:g.44193128_44193130del GRCh37
NC_000007.12:g.44159653_44159655del NCBI36
NG_008847.1:g.40893_40895del
NG_008847.2:g.49640_49642del

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*44-68_*44-66del ENSP00000379142.4:n.*44-68_*44-66del
ENST00000616242.5:c.46-68_46-66del ENSP00000482149.2:n.46-68_46-66del
ENST00000682635.1:n.532-68_532-66del
ENST00000345378.7:c.49-68_49-66del ENSP00000223366.2:n.49-68_49-66del
ENST00000403799.8:c.46-68_46-66del MANE Select ENSP00000384247.3:n.46-68_46-66del
ENST00000671824.1:c.46-68_46-66del ENSP00000500264.1:n.46-68_46-66del
ENST00000673284.1:c.46-68_46-66del ENSP00000499852.1:n.46-68_46-66del
ENST00000345378.6:c.49-68_49-66del ENSP00000223366.2:n.49-68_49-66del
ENST00000395796.7:c.43-68_43-66del ENSP00000379142.3:n.43-68_43-66del
ENST00000403799.7:c.46-68_46-66del ENSP00000384247.3:n.46-68_46-66del
ENST00000437084.1:c.46-68_46-66del ENSP00000402840.1:n.46-68_46-66del
ENST00000476008.1:n.481-68_481-66del
ENST00000616242.4:c.43-68_43-66del ENSP00000482149.1:n.43-68_43-66del
NM_000162.3:c.46-68_46-66del NP_000153.1:n.46-68_46-66del
NM_033507.1:c.49-68_49-66del NP_277042.1:n.49-68_49-66del
NM_033508.1:c.43-68_43-66del NP_277043.1:n.43-68_43-66del
NM_000162.4:c.46-68_46-66del NP_000153.1:n.46-68_46-66del
NM_001354800.1:c.46-68_46-66del NP_001341729.1:n.46-68_46-66del
NM_033507.2:c.49-68_49-66del NP_277042.1:n.49-68_49-66del
NM_033508.2:c.43-68_43-66del NP_277043.1:n.43-68_43-66del
NM_000162.5:c.46-68_46-66del MANE Select NP_000153.1:n.46-68_46-66del
NM_033507.3:c.49-68_49-66del NP_277042.1:n.49-68_49-66del
NM_033508.3:c.43-68_43-66del NP_277043.1:n.43-68_43-66del
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