Canonical Allele Identifier: CA367399177
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44145684-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145684C>T , CM000669.2:g.44145684C>T GRCh38
NC_000007.13:g.44185283C>T , CM000669.1:g.44185283C>T GRCh37
NC_000007.12:g.44151808C>T NCBI36
NG_008847.1:g.48740G>A
NG_008847.2:g.57487G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1064G>A ENSP00000379142.4:n.*1064G>A
ENST00000616242.5:c.*186G>A ENSP00000482149.2:n.*186G>A
ENST00000683378.1:n.292G>A
ENST00000336642.9:c.100G>A ENSP00000338009.5:p.Gly34Arg
ENST00000345378.7:c.1069G>A ENSP00000223366.2:p.Gly357Arg
ENST00000403799.8:c.1066G>A MANE Select ENSP00000384247.3:p.Gly356Arg
ENST00000671824.1:c.1129G>A ENSP00000500264.1:p.Gly377Arg
ENST00000672743.1:n.78G>A
ENST00000673284.1:c.1066G>A ENSP00000499852.1:p.Gly356Arg
ENST00000336642.8:c.118G>A ENSP00000338009.4:p.Gly40Arg
ENST00000345378.6:c.1069G>A ENSP00000223366.2:p.Gly357Arg
ENST00000395796.7:c.1063G>A ENSP00000379142.3:p.Gly355Arg
ENST00000403799.7:c.1066G>A ENSP00000384247.3:p.Gly356Arg
ENST00000437084.1:c.1015G>A ENSP00000402840.1:p.Gly339Arg
ENST00000459642.1:n.446G>A
ENST00000473353.1:n.364G>A
ENST00000616242.4:c.1063G>A ENSP00000482149.1:p.Gly355Arg
NM_000162.3:c.1066G>A NP_000153.1:p.Gly356Arg
NM_033507.1:c.1069G>A NP_277042.1:p.Gly357Arg
NM_033508.1:c.1063G>A NP_277043.1:p.Gly355Arg
NM_000162.4:c.1066G>A NP_000153.1:p.Gly356Arg
NM_001354800.1:c.1066G>A NP_001341729.1:p.Gly356Arg
NM_001354801.1:c.55G>A NP_001341730.1:p.Gly19Arg
NM_001354802.1:c.-75G>A NP_001341731.1:n.-75G>A
NM_001354803.1:c.100G>A NP_001341732.1:p.Gly34Arg
NM_033507.2:c.1069G>A NP_277042.1:p.Gly357Arg
NM_033508.2:c.1063G>A NP_277043.1:p.Gly355Arg
XM_024446707.1:c.-75G>A XP_024302475.1:n.-75G>A
NM_000162.5:c.1066G>A MANE Select NP_000153.1:p.Gly356Arg
NM_033507.3:c.1069G>A NP_277042.1:p.Gly357Arg
NM_033508.3:c.1063G>A NP_277043.1:p.Gly355Arg
NM_001354803.2:c.100G>A NP_001341732.1:p.Gly34Arg