Canonical Allele Identifier: CA1703637535
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44153358C= , CM000669.2:g.44153358C= GRCh38
NC_000007.13:g.44192957C= , CM000669.1:g.44192957C= GRCh37
NC_000007.12:g.44159482C= NCBI36
NG_008847.1:g.41066G=
NG_008847.2:g.49813G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*149G= ENSP00000379142.4:n.*149G=
ENST00000616242.5:c.151G= ENSP00000482149.2:p.Glu51=
ENST00000682635.1:n.637G=
ENST00000345378.7:c.154G= ENSP00000223366.2:p.Glu52=
ENST00000403799.8:c.151G= MANE Select ENSP00000384247.3:p.Glu51=
ENST00000671824.1:c.151G= ENSP00000500264.1:p.Glu51=
ENST00000673284.1:c.151G= ENSP00000499852.1:p.Glu51=
ENST00000345378.6:c.154G= ENSP00000223366.2:p.Glu52=
ENST00000395796.7:c.148G= ENSP00000379142.3:p.Glu50=
ENST00000403799.7:c.151G= ENSP00000384247.3:p.Glu51=
ENST00000437084.1:c.151G= ENSP00000402840.1:p.Glu51=
ENST00000616242.4:c.148G= ENSP00000482149.1:p.Glu50=
NM_000162.3:c.151G= NP_000153.1:p.Glu51=
NM_033507.1:c.154G= NP_277042.1:p.Glu52=
NM_033508.1:c.148G= NP_277043.1:p.Glu50=
NM_000162.4:c.151G= NP_000153.1:p.Glu51=
NM_001354800.1:c.151G= NP_001341729.1:p.Glu51=
NM_033507.2:c.154G= NP_277042.1:p.Glu52=
NM_033508.2:c.148G= NP_277043.1:p.Glu50=
NM_000162.5:c.151G= MANE Select NP_000153.1:p.Glu51=
NM_033507.3:c.154G= NP_277042.1:p.Glu52=
NM_033508.3:c.148G= NP_277043.1:p.Glu50=
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