Canonical Allele Identifier: CA1703612954
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145682C= , CM000669.2:g.44145682C= GRCh38
NC_000007.13:g.44185281C= , CM000669.1:g.44185281C= GRCh37
NC_000007.12:g.44151806C= NCBI36
NG_008847.1:g.48742G=
NG_008847.2:g.57489G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1066G= ENSP00000379142.4:n.*1066G=
ENST00000616242.5:c.*188G= ENSP00000482149.2:n.*188G=
ENST00000683378.1:n.294G=
ENST00000336642.9:c.102G= ENSP00000338009.5:p.Gly34=
ENST00000345378.7:c.1071G= ENSP00000223366.2:p.Gly357=
ENST00000403799.8:c.1068G= MANE Select ENSP00000384247.3:p.Gly356=
ENST00000671824.1:c.1131G= ENSP00000500264.1:p.Gly377=
ENST00000672743.1:n.80G=
ENST00000673284.1:c.1068G= ENSP00000499852.1:p.Gly356=
ENST00000336642.8:c.120G= ENSP00000338009.4:p.Gly40=
ENST00000345378.6:c.1071G= ENSP00000223366.2:p.Gly357=
ENST00000395796.7:c.1065G= ENSP00000379142.3:p.Gly355=
ENST00000403799.7:c.1068G= ENSP00000384247.3:p.Gly356=
ENST00000437084.1:c.1017G= ENSP00000402840.1:p.Gly339=
ENST00000459642.1:n.448G=
ENST00000473353.1:n.366G=
ENST00000616242.4:c.1065G= ENSP00000482149.1:p.Gly355=
NM_000162.3:c.1068G= NP_000153.1:p.Gly356=
NM_033507.1:c.1071G= NP_277042.1:p.Gly357=
NM_033508.1:c.1065G= NP_277043.1:p.Gly355=
NM_000162.4:c.1068G= NP_000153.1:p.Gly356=
NM_001354800.1:c.1068G= NP_001341729.1:p.Gly356=
NM_001354801.1:c.57G= NP_001341730.1:p.Gly19=
NM_001354802.1:c.-73G= NP_001341731.1:n.-73G=
NM_001354803.1:c.102G= NP_001341732.1:p.Gly34=
NM_033507.2:c.1071G= NP_277042.1:p.Gly357=
NM_033508.2:c.1065G= NP_277043.1:p.Gly355=
XM_024446707.1:c.-73G= XP_024302475.1:n.-73G=
NM_000162.5:c.1068G= MANE Select NP_000153.1:p.Gly356=
NM_033507.3:c.1071G= NP_277042.1:p.Gly357=
NM_033508.3:c.1065G= NP_277043.1:p.Gly355=
NM_001354803.2:c.102G= NP_001341732.1:p.Gly34=