Canonical Allele Identifier: CA2682579977
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44145057-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145057C>T , CM000669.2:g.44145057C>T GRCh38
NC_000007.13:g.44184656C>T , CM000669.1:g.44184656C>T GRCh37
NC_000007.12:g.44151181C>T NCBI36
NG_008847.1:g.49367G>A
NG_008847.2:g.58114G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1475G>A ENSP00000379142.4:n.*1475G>A
ENST00000616242.5:c.*597G>A ENSP00000482149.2:n.*597G>A
ENST00000683378.1:n.703G>A
ENST00000336642.9:c.*79G>A ENSP00000338009.5:n.*79G>A
ENST00000345378.7:c.*79G>A ENSP00000223366.2:n.*79G>A
ENST00000403799.8:c.*79G>A MANE Select ENSP00000384247.3:n.*79G>A
ENST00000671824.1:c.*79G>A ENSP00000500264.1:n.*79G>A
ENST00000672743.1:n.381+108G>A
ENST00000673284.1:c.1369+108G>A ENSP00000499852.1:n.1369+108G>A
ENST00000336642.8:c.529G>A ENSP00000338009.4:n.529G>A
ENST00000345378.6:c.*79G>A ENSP00000223366.2:n.*79G>A
ENST00000395796.7:c.*79G>A ENSP00000379142.3:n.*79G>A
ENST00000403799.7:c.*79G>A ENSP00000384247.3:n.*79G>A
ENST00000459642.1:n.857G>A
ENST00000616242.4:c.1474G>A ENSP00000482149.1:n.1474G>A
NM_000162.3:c.*79G>A NP_000153.1:n.*79G>A
NM_033507.1:c.*79G>A NP_277042.1:n.*79G>A
NM_033508.1:c.*79G>A NP_277043.1:n.*79G>A
NM_000162.4:c.*79G>A NP_000153.1:n.*79G>A
NM_001354800.1:c.1369+108G>A NP_001341729.1:n.1369+108G>A
NM_001354801.1:c.*79G>A NP_001341730.1:n.*79G>A
NM_001354802.1:c.229+108G>A NP_001341731.1:n.229+108G>A
NM_001354803.1:c.*79G>A NP_001341732.1:n.*79G>A
NM_033507.2:c.*79G>A NP_277042.1:n.*79G>A
NM_033508.2:c.*79G>A NP_277043.1:n.*79G>A
XM_024446707.1:c.*79G>A XP_024302475.1:n.*79G>A
NM_000162.5:c.*79G>A MANE Select NP_000153.1:n.*79G>A
NM_033507.3:c.*79G>A NP_277042.1:n.*79G>A
NM_033508.3:c.*79G>A NP_277043.1:n.*79G>A
NM_001354803.2:c.*79G>A NP_001341732.1:n.*79G>A
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