Canonical Allele Identifier: CA1703612873
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145560C= , CM000669.2:g.44145560C= GRCh38
NC_000007.13:g.44185159C= , CM000669.1:g.44185159C= GRCh37
NC_000007.12:g.44151684C= NCBI36
NG_008847.1:g.48864G=
NG_008847.2:g.57611G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1188G= ENSP00000379142.4:n.*1188G=
ENST00000616242.5:c.*310G= ENSP00000482149.2:n.*310G=
ENST00000683378.1:n.416G=
ENST00000336642.9:c.224G= ENSP00000338009.5:p.Arg75=
ENST00000345378.7:c.1193G= ENSP00000223366.2:p.Arg398=
ENST00000403799.8:c.1190G= MANE Select ENSP00000384247.3:p.Arg397=
ENST00000671824.1:c.1253G= ENSP00000500264.1:p.Arg418=
ENST00000672743.1:n.202G=
ENST00000673284.1:c.1190G= ENSP00000499852.1:p.Arg397=
ENST00000336642.8:c.242G= ENSP00000338009.4:p.Arg81=
ENST00000345378.6:c.1193G= ENSP00000223366.2:p.Arg398=
ENST00000395796.7:c.1187G= ENSP00000379142.3:p.Arg396=
ENST00000403799.7:c.1190G= ENSP00000384247.3:p.Arg397=
ENST00000437084.1:c.1139G= ENSP00000402840.1:p.Arg380=
ENST00000459642.1:n.570G=
ENST00000616242.4:c.1187G= ENSP00000482149.1:p.Arg396=
NM_000162.3:c.1190G= NP_000153.1:p.Arg397=
NM_033507.1:c.1193G= NP_277042.1:p.Arg398=
NM_033508.1:c.1187G= NP_277043.1:p.Arg396=
NM_000162.4:c.1190G= NP_000153.1:p.Arg397=
NM_001354800.1:c.1190G= NP_001341729.1:p.Arg397=
NM_001354801.1:c.179G= NP_001341730.1:p.Arg60=
NM_001354802.1:c.50G= NP_001341731.1:p.Arg17=
NM_001354803.1:c.224G= NP_001341732.1:p.Arg75=
NM_033507.2:c.1193G= NP_277042.1:p.Arg398=
NM_033508.2:c.1187G= NP_277043.1:p.Arg396=
XM_024446707.1:c.50G= XP_024302475.1:p.Arg17=
NM_000162.5:c.1190G= MANE Select NP_000153.1:p.Arg397=
NM_033507.3:c.1193G= NP_277042.1:p.Arg398=
NM_033508.3:c.1187G= NP_277043.1:p.Arg396=
NM_001354803.2:c.224G= NP_001341732.1:p.Arg75=