Canonical Allele Identifier: CA2682578841
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44144794-TG-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44144797del , CM000669.2:g.44144797del GRCh38
NC_000007.13:g.44184396del , CM000669.1:g.44184396del GRCh37
NC_000007.12:g.44150921del NCBI36
NG_008847.1:g.49629del
NG_008847.2:g.58376del

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1737del ENSP00000379142.4:n.*1737del
ENST00000616242.5:c.*859del ENSP00000482149.2:n.*859del
ENST00000683378.1:n.965del
ENST00000336642.9:c.*341del ENSP00000338009.5:n.*341del
ENST00000345378.7:c.*341del ENSP00000223366.2:n.*341del
ENST00000403799.8:c.*341del MANE Select ENSP00000384247.3:n.*341del
ENST00000671824.1:c.*341del ENSP00000500264.1:n.*341del
ENST00000672743.1:n.381+370del
ENST00000673284.1:c.1369+370del ENSP00000499852.1:n.1369+370del
ENST00000336642.8:c.791del ENSP00000338009.4:n.791del
ENST00000345378.6:c.*341del ENSP00000223366.2:n.*341del
ENST00000395796.7:c.*341del ENSP00000379142.3:n.*341del
ENST00000403799.7:c.*341del ENSP00000384247.3:n.*341del
ENST00000459642.1:n.1119del
ENST00000616242.4:c.1736del ENSP00000482149.1:n.1736del
NM_000162.3:c.*341del NP_000153.1:n.*341del
NM_033507.1:c.*341del NP_277042.1:n.*341del
NM_033508.1:c.*341del NP_277043.1:n.*341del
NM_000162.4:c.*341del NP_000153.1:n.*341del
NM_001354800.1:c.1369+370del NP_001341729.1:n.1369+370del
NM_001354801.1:c.*341del NP_001341730.1:n.*341del
NM_001354802.1:c.229+370del NP_001341731.1:n.229+370del
NM_001354803.1:c.*341del NP_001341732.1:n.*341del
NM_033507.2:c.*341del NP_277042.1:n.*341del
NM_033508.2:c.*341del NP_277043.1:n.*341del
XM_024446707.1:c.*341del XP_024302475.1:n.*341del
NM_000162.5:c.*341del MANE Select NP_000153.1:n.*341del
NM_033507.3:c.*341del NP_277042.1:n.*341del
NM_033508.3:c.*341del NP_277043.1:n.*341del
NM_001354803.2:c.*341del NP_001341732.1:n.*341del
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