Canonical Allele Identifier: CA1703612876
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145565C= , CM000669.2:g.44145565C= GRCh38
NC_000007.13:g.44185164C= , CM000669.1:g.44185164C= GRCh37
NC_000007.12:g.44151689C= NCBI36
NG_008847.1:g.48859G=
NG_008847.2:g.57606G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1183G= ENSP00000379142.4:n.*1183G=
ENST00000616242.5:c.*305G= ENSP00000482149.2:n.*305G=
ENST00000683378.1:n.411G=
ENST00000336642.9:c.219G= ENSP00000338009.5:p.Glu73=
ENST00000345378.7:c.1188G= ENSP00000223366.2:p.Glu396=
ENST00000403799.8:c.1185G= MANE Select ENSP00000384247.3:p.Glu395=
ENST00000671824.1:c.1248G= ENSP00000500264.1:p.Glu416=
ENST00000672743.1:n.197G=
ENST00000673284.1:c.1185G= ENSP00000499852.1:p.Glu395=
ENST00000336642.8:c.237G= ENSP00000338009.4:p.Glu79=
ENST00000345378.6:c.1188G= ENSP00000223366.2:p.Glu396=
ENST00000395796.7:c.1182G= ENSP00000379142.3:p.Glu394=
ENST00000403799.7:c.1185G= ENSP00000384247.3:p.Glu395=
ENST00000437084.1:c.1134G= ENSP00000402840.1:p.Glu378=
ENST00000459642.1:n.565G=
ENST00000616242.4:c.1182G= ENSP00000482149.1:p.Glu394=
NM_000162.3:c.1185G= NP_000153.1:p.Glu395=
NM_033507.1:c.1188G= NP_277042.1:p.Glu396=
NM_033508.1:c.1182G= NP_277043.1:p.Glu394=
NM_000162.4:c.1185G= NP_000153.1:p.Glu395=
NM_001354800.1:c.1185G= NP_001341729.1:p.Glu395=
NM_001354801.1:c.174G= NP_001341730.1:p.Glu58=
NM_001354802.1:c.45G= NP_001341731.1:p.Glu15=
NM_001354803.1:c.219G= NP_001341732.1:p.Glu73=
NM_033507.2:c.1188G= NP_277042.1:p.Glu396=
NM_033508.2:c.1182G= NP_277043.1:p.Glu394=
XM_024446707.1:c.45G= XP_024302475.1:p.Glu15=
NM_000162.5:c.1185G= MANE Select NP_000153.1:p.Glu395=
NM_033507.3:c.1188G= NP_277042.1:p.Glu396=
NM_033508.3:c.1182G= NP_277043.1:p.Glu394=
NM_001354803.2:c.219G= NP_001341732.1:p.Glu73=