Canonical Allele Identifier: CA1703636451
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44150992G= , CM000669.2:g.44150992G= GRCh38
NC_000007.13:g.44190591G= , CM000669.1:g.44190591G= GRCh37
NC_000007.12:g.44157116G= NCBI36
NG_008847.1:g.43432C=
NG_008847.2:g.52179C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*445C= ENSP00000379142.4:n.*445C=
ENST00000616242.5:c.447C= ENSP00000482149.2:p.Thr149=
ENST00000682635.1:n.933C=
ENST00000345378.7:c.450C= ENSP00000223366.2:p.Thr150=
ENST00000403799.8:c.447C= MANE Select ENSP00000384247.3:p.Thr149=
ENST00000671824.1:c.447C= ENSP00000500264.1:p.Thr149=
ENST00000673284.1:c.447C= ENSP00000499852.1:p.Thr149=
ENST00000345378.6:c.450C= ENSP00000223366.2:p.Thr150=
ENST00000395796.7:c.444C= ENSP00000379142.3:p.Thr148=
ENST00000403799.7:c.447C= ENSP00000384247.3:p.Thr149=
ENST00000437084.1:c.396C= ENSP00000402840.1:p.Thr132=
ENST00000616242.4:c.444C= ENSP00000482149.1:p.Thr148=
NM_000162.3:c.447C= NP_000153.1:p.Thr149=
NM_033507.1:c.450C= NP_277042.1:p.Thr150=
NM_033508.1:c.444C= NP_277043.1:p.Thr148=
NM_000162.4:c.447C= NP_000153.1:p.Thr149=
NM_001354800.1:c.447C= NP_001341729.1:p.Thr149=
NM_033507.2:c.450C= NP_277042.1:p.Thr150=
NM_033508.2:c.444C= NP_277043.1:p.Thr148=
NM_000162.5:c.447C= MANE Select NP_000153.1:p.Thr149=
NM_033507.3:c.450C= NP_277042.1:p.Thr150=
NM_033508.3:c.444C= NP_277043.1:p.Thr148=
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