Canonical Allele Identifier: CA1703637534
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44153357T= , CM000669.2:g.44153357T= GRCh38
NC_000007.13:g.44192956T= , CM000669.1:g.44192956T= GRCh37
NC_000007.12:g.44159481T= NCBI36
NG_008847.1:g.41067A=
NG_008847.2:g.49814A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*150A= ENSP00000379142.4:n.*150A=
ENST00000616242.5:c.152A= ENSP00000482149.2:p.Glu51=
ENST00000682635.1:n.638A=
ENST00000345378.7:c.155A= ENSP00000223366.2:p.Glu52=
ENST00000403799.8:c.152A= MANE Select ENSP00000384247.3:p.Glu51=
ENST00000671824.1:c.152A= ENSP00000500264.1:p.Glu51=
ENST00000673284.1:c.152A= ENSP00000499852.1:p.Glu51=
ENST00000345378.6:c.155A= ENSP00000223366.2:p.Glu52=
ENST00000395796.7:c.149A= ENSP00000379142.3:p.Glu50=
ENST00000403799.7:c.152A= ENSP00000384247.3:p.Glu51=
ENST00000437084.1:c.152A= ENSP00000402840.1:p.Glu51=
ENST00000616242.4:c.149A= ENSP00000482149.1:p.Glu50=
NM_000162.3:c.152A= NP_000153.1:p.Glu51=
NM_033507.1:c.155A= NP_277042.1:p.Glu52=
NM_033508.1:c.149A= NP_277043.1:p.Glu50=
NM_000162.4:c.152A= NP_000153.1:p.Glu51=
NM_001354800.1:c.152A= NP_001341729.1:p.Glu51=
NM_033507.2:c.155A= NP_277042.1:p.Glu52=
NM_033508.2:c.149A= NP_277043.1:p.Glu50=
NM_000162.5:c.152A= MANE Select NP_000153.1:p.Glu51=
NM_033507.3:c.155A= NP_277042.1:p.Glu52=
NM_033508.3:c.149A= NP_277043.1:p.Glu50=
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