Canonical Allele Identifier: CA1703612670
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145195G= , CM000669.2:g.44145195G= GRCh38
NC_000007.13:g.44184794G= , CM000669.1:g.44184794G= GRCh37
NC_000007.12:g.44151319G= NCBI36
NG_008847.1:g.49229C=
NG_008847.2:g.57976C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1337C= ENSP00000379142.4:n.*1337C=
ENST00000616242.5:c.*459C= ENSP00000482149.2:n.*459C=
ENST00000683378.1:n.565C=
ENST00000336642.9:c.373C= ENSP00000338009.5:p.Arg125=
ENST00000345378.7:c.1342C= ENSP00000223366.2:p.Arg448=
ENST00000403799.8:c.1339C= MANE Select ENSP00000384247.3:p.Arg447=
ENST00000671824.1:c.1402C= ENSP00000500264.1:p.Arg468=
ENST00000672743.1:n.351C=
ENST00000673284.1:c.1339C= ENSP00000499852.1:p.Arg447=
ENST00000336642.8:c.391C= ENSP00000338009.4:p.Arg131=
ENST00000345378.6:c.1342C= ENSP00000223366.2:p.Arg448=
ENST00000395796.7:c.1336C= ENSP00000379142.3:p.Arg446=
ENST00000403799.7:c.1339C= ENSP00000384247.3:p.Arg447=
ENST00000437084.1:c.1288C= ENSP00000402840.1:p.Arg430=
ENST00000459642.1:n.719C=
ENST00000616242.4:c.1336C= ENSP00000482149.1:p.Arg446=
NM_000162.3:c.1339C= NP_000153.1:p.Arg447=
NM_033507.1:c.1342C= NP_277042.1:p.Arg448=
NM_033508.1:c.1336C= NP_277043.1:p.Arg446=
NM_000162.4:c.1339C= NP_000153.1:p.Arg447=
NM_001354800.1:c.1339C= NP_001341729.1:p.Arg447=
NM_001354801.1:c.328C= NP_001341730.1:p.Arg110=
NM_001354802.1:c.199C= NP_001341731.1:p.Arg67=
NM_001354803.1:c.373C= NP_001341732.1:p.Arg125=
NM_033507.2:c.1342C= NP_277042.1:p.Arg448=
NM_033508.2:c.1336C= NP_277043.1:p.Arg446=
XM_024446707.1:c.199C= XP_024302475.1:p.Arg67=
NM_000162.5:c.1339C= MANE Select NP_000153.1:p.Arg447=
NM_033507.3:c.1342C= NP_277042.1:p.Arg448=
NM_033508.3:c.1336C= NP_277043.1:p.Arg446=
NM_001354803.2:c.373C= NP_001341732.1:p.Arg125=