Canonical Allele Identifier: CA1703612888
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145582T= , CM000669.2:g.44145582T= GRCh38
NC_000007.13:g.44185181T= , CM000669.1:g.44185181T= GRCh37
NC_000007.12:g.44151706T= NCBI36
NG_008847.1:g.48842A=
NG_008847.2:g.57589A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1166A= ENSP00000379142.4:n.*1166A=
ENST00000616242.5:c.*288A= ENSP00000482149.2:n.*288A=
ENST00000683378.1:n.394A=
ENST00000336642.9:c.202A= ENSP00000338009.5:p.Ile68=
ENST00000345378.7:c.1171A= ENSP00000223366.2:p.Ile391=
ENST00000403799.8:c.1168A= MANE Select ENSP00000384247.3:p.Ile390=
ENST00000671824.1:c.1231A= ENSP00000500264.1:p.Ile411=
ENST00000672743.1:n.180A=
ENST00000673284.1:c.1168A= ENSP00000499852.1:p.Ile390=
ENST00000336642.8:c.220A= ENSP00000338009.4:p.Ile74=
ENST00000345378.6:c.1171A= ENSP00000223366.2:p.Ile391=
ENST00000395796.7:c.1165A= ENSP00000379142.3:p.Ile389=
ENST00000403799.7:c.1168A= ENSP00000384247.3:p.Ile390=
ENST00000437084.1:c.1117A= ENSP00000402840.1:p.Ile373=
ENST00000459642.1:n.548A=
ENST00000616242.4:c.1165A= ENSP00000482149.1:p.Ile389=
NM_000162.3:c.1168A= NP_000153.1:p.Ile390=
NM_033507.1:c.1171A= NP_277042.1:p.Ile391=
NM_033508.1:c.1165A= NP_277043.1:p.Ile389=
NM_000162.4:c.1168A= NP_000153.1:p.Ile390=
NM_001354800.1:c.1168A= NP_001341729.1:p.Ile390=
NM_001354801.1:c.157A= NP_001341730.1:p.Ile53=
NM_001354802.1:c.28A= NP_001341731.1:p.Ile10=
NM_001354803.1:c.202A= NP_001341732.1:p.Ile68=
NM_033507.2:c.1171A= NP_277042.1:p.Ile391=
NM_033508.2:c.1165A= NP_277043.1:p.Ile389=
XM_024446707.1:c.28A= XP_024302475.1:p.Ile10=
NM_000162.5:c.1168A= MANE Select NP_000153.1:p.Ile390=
NM_033507.3:c.1171A= NP_277042.1:p.Ile391=
NM_033508.3:c.1165A= NP_277043.1:p.Ile389=
NM_001354803.2:c.202A= NP_001341732.1:p.Ile68=