Canonical Allele Identifier: CA367399145
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44145678-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145678G>C , CM000669.2:g.44145678G>C GRCh38
NC_000007.13:g.44185277G>C , CM000669.1:g.44185277G>C GRCh37
NC_000007.12:g.44151802G>C NCBI36
NG_008847.1:g.48746C>G
NG_008847.2:g.57493C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1070C>G ENSP00000379142.4:n.*1070C>G
ENST00000616242.5:c.*192C>G ENSP00000482149.2:n.*192C>G
ENST00000683378.1:n.298C>G
ENST00000336642.9:c.106C>G ENSP00000338009.5:p.Arg36Gly
ENST00000345378.7:c.1075C>G ENSP00000223366.2:p.Arg359Gly
ENST00000403799.8:c.1072C>G MANE Select ENSP00000384247.3:p.Arg358Gly
ENST00000671824.1:c.1135C>G ENSP00000500264.1:p.Arg379Gly
ENST00000672743.1:n.84C>G
ENST00000673284.1:c.1072C>G ENSP00000499852.1:p.Arg358Gly
ENST00000336642.8:c.124C>G ENSP00000338009.4:p.Arg42Gly
ENST00000345378.6:c.1075C>G ENSP00000223366.2:p.Arg359Gly
ENST00000395796.7:c.1069C>G ENSP00000379142.3:p.Arg357Gly
ENST00000403799.7:c.1072C>G ENSP00000384247.3:p.Arg358Gly
ENST00000437084.1:c.1021C>G ENSP00000402840.1:p.Arg341Gly
ENST00000459642.1:n.452C>G
ENST00000473353.1:n.370C>G
ENST00000616242.4:c.1069C>G ENSP00000482149.1:p.Arg357Gly
NM_000162.3:c.1072C>G NP_000153.1:p.Arg358Gly
NM_033507.1:c.1075C>G NP_277042.1:p.Arg359Gly
NM_033508.1:c.1069C>G NP_277043.1:p.Arg357Gly
NM_000162.4:c.1072C>G NP_000153.1:p.Arg358Gly
NM_001354800.1:c.1072C>G NP_001341729.1:p.Arg358Gly
NM_001354801.1:c.61C>G NP_001341730.1:p.Arg21Gly
NM_001354802.1:c.-69C>G NP_001341731.1:n.-69C>G
NM_001354803.1:c.106C>G NP_001341732.1:p.Arg36Gly
NM_033507.2:c.1075C>G NP_277042.1:p.Arg359Gly
NM_033508.2:c.1069C>G NP_277043.1:p.Arg357Gly
XM_024446707.1:c.-69C>G XP_024302475.1:n.-69C>G
NM_000162.5:c.1072C>G MANE Select NP_000153.1:p.Arg358Gly
NM_033507.3:c.1075C>G NP_277042.1:p.Arg359Gly
NM_033508.3:c.1069C>G NP_277043.1:p.Arg357Gly
NM_001354803.2:c.106C>G NP_001341732.1:p.Arg36Gly