Canonical Allele Identifier: CA2682579918
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44145050-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145050C>A , CM000669.2:g.44145050C>A GRCh38
NC_000007.13:g.44184649C>A , CM000669.1:g.44184649C>A GRCh37
NC_000007.12:g.44151174C>A NCBI36
NG_008847.1:g.49374G>T
NG_008847.2:g.58121G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1482G>T ENSP00000379142.4:n.*1482G>T
ENST00000616242.5:c.*604G>T ENSP00000482149.2:n.*604G>T
ENST00000683378.1:n.710G>T
ENST00000336642.9:c.*86G>T ENSP00000338009.5:n.*86G>T
ENST00000345378.7:c.*86G>T ENSP00000223366.2:n.*86G>T
ENST00000403799.8:c.*86G>T MANE Select ENSP00000384247.3:n.*86G>T
ENST00000671824.1:c.*86G>T ENSP00000500264.1:n.*86G>T
ENST00000672743.1:n.381+115G>T
ENST00000673284.1:c.1369+115G>T ENSP00000499852.1:n.1369+115G>T
ENST00000336642.8:c.536G>T ENSP00000338009.4:n.536G>T
ENST00000345378.6:c.*86G>T ENSP00000223366.2:n.*86G>T
ENST00000395796.7:c.*86G>T ENSP00000379142.3:n.*86G>T
ENST00000403799.7:c.*86G>T ENSP00000384247.3:n.*86G>T
ENST00000459642.1:n.864G>T
ENST00000616242.4:c.1481G>T ENSP00000482149.1:n.1481G>T
NM_000162.3:c.*86G>T NP_000153.1:n.*86G>T
NM_033507.1:c.*86G>T NP_277042.1:n.*86G>T
NM_033508.1:c.*86G>T NP_277043.1:n.*86G>T
NM_000162.4:c.*86G>T NP_000153.1:n.*86G>T
NM_001354800.1:c.1369+115G>T NP_001341729.1:n.1369+115G>T
NM_001354801.1:c.*86G>T NP_001341730.1:n.*86G>T
NM_001354802.1:c.229+115G>T NP_001341731.1:n.229+115G>T
NM_001354803.1:c.*86G>T NP_001341732.1:n.*86G>T
NM_033507.2:c.*86G>T NP_277042.1:n.*86G>T
NM_033508.2:c.*86G>T NP_277043.1:n.*86G>T
XM_024446707.1:c.*86G>T XP_024302475.1:n.*86G>T
NM_000162.5:c.*86G>T MANE Select NP_000153.1:n.*86G>T
NM_033507.3:c.*86G>T NP_277042.1:n.*86G>T
NM_033508.3:c.*86G>T NP_277043.1:n.*86G>T
NM_001354803.2:c.*86G>T NP_001341732.1:n.*86G>T
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