Canonical Allele Identifier: CA1703636463
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44151008A= , CM000669.2:g.44151008A= GRCh38
NC_000007.13:g.44190607A= , CM000669.1:g.44190607A= GRCh37
NC_000007.12:g.44157132A= NCBI36
NG_008847.1:g.43416T=
NG_008847.2:g.52163T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*429T= ENSP00000379142.4:n.*429T=
ENST00000616242.5:c.431T= ENSP00000482149.2:p.Leu144=
ENST00000682635.1:n.917T=
ENST00000345378.7:c.434T= ENSP00000223366.2:p.Leu145=
ENST00000403799.8:c.431T= MANE Select ENSP00000384247.3:p.Leu144=
ENST00000671824.1:c.431T= ENSP00000500264.1:p.Leu144=
ENST00000673284.1:c.431T= ENSP00000499852.1:p.Leu144=
ENST00000345378.6:c.434T= ENSP00000223366.2:p.Leu145=
ENST00000395796.7:c.428T= ENSP00000379142.3:p.Leu143=
ENST00000403799.7:c.431T= ENSP00000384247.3:p.Leu144=
ENST00000437084.1:c.380T= ENSP00000402840.1:p.Leu127=
ENST00000616242.4:c.428T= ENSP00000482149.1:p.Leu143=
NM_000162.3:c.431T= NP_000153.1:p.Leu144=
NM_033507.1:c.434T= NP_277042.1:p.Leu145=
NM_033508.1:c.428T= NP_277043.1:p.Leu143=
NM_000162.4:c.431T= NP_000153.1:p.Leu144=
NM_001354800.1:c.431T= NP_001341729.1:p.Leu144=
NM_033507.2:c.434T= NP_277042.1:p.Leu145=
NM_033508.2:c.428T= NP_277043.1:p.Leu143=
NM_000162.5:c.431T= MANE Select NP_000153.1:p.Leu144=
NM_033507.3:c.434T= NP_277042.1:p.Leu145=
NM_033508.3:c.428T= NP_277043.1:p.Leu143=
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