Canonical Allele Identifier: CA2775231705
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44144787del , CM000669.2:g.44144787del GRCh38
NC_000007.13:g.44184386del , CM000669.1:g.44184386del GRCh37
NC_000007.12:g.44150911del NCBI36
NG_008847.1:g.49639del
NG_008847.2:g.58386del

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1747del ENSP00000379142.4:n.*1747del
ENST00000616242.5:c.*869del ENSP00000482149.2:n.*869del
ENST00000683378.1:n.975del
ENST00000336642.9:c.*351del ENSP00000338009.5:n.*351del
ENST00000345378.7:c.*351del ENSP00000223366.2:n.*351del
ENST00000403799.8:c.*351del MANE Select ENSP00000384247.3:n.*351del
ENST00000671824.1:c.*351del ENSP00000500264.1:n.*351del
ENST00000672743.1:n.381+380del
ENST00000673284.1:c.1369+380del ENSP00000499852.1:n.1369+380del
ENST00000336642.8:c.801del ENSP00000338009.4:n.801del
ENST00000345378.6:c.*351del ENSP00000223366.2:n.*351del
ENST00000395796.7:c.*351del ENSP00000379142.3:n.*351del
ENST00000403799.7:c.*351del ENSP00000384247.3:n.*351del
ENST00000459642.1:n.1129del
ENST00000616242.4:c.1746del ENSP00000482149.1:n.1746del
NM_000162.3:c.*351del NP_000153.1:n.*351del
NM_033507.1:c.*351del NP_277042.1:n.*351del
NM_033508.1:c.*351del NP_277043.1:n.*351del
NM_000162.4:c.*351del NP_000153.1:n.*351del
NM_001354800.1:c.1369+380del NP_001341729.1:n.1369+380del
NM_001354801.1:c.*351del NP_001341730.1:n.*351del
NM_001354802.1:c.229+380del NP_001341731.1:n.229+380del
NM_001354803.1:c.*351del NP_001341732.1:n.*351del
NM_033507.2:c.*351del NP_277042.1:n.*351del
NM_033508.2:c.*351del NP_277043.1:n.*351del
XM_024446707.1:c.*351del XP_024302475.1:n.*351del
NM_000162.5:c.*351del MANE Select NP_000153.1:n.*351del
NM_033507.3:c.*351del NP_277042.1:n.*351del
NM_033508.3:c.*351del NP_277043.1:n.*351del
NM_001354803.2:c.*351del NP_001341732.1:n.*351del
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