Canonical Allele Identifier: CA1703636446
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44150980A= , CM000669.2:g.44150980A= GRCh38
NC_000007.13:g.44190579A= , CM000669.1:g.44190579A= GRCh37
NC_000007.12:g.44157104A= NCBI36
NG_008847.1:g.43444T=
NG_008847.2:g.52191T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*457T= ENSP00000379142.4:n.*457T=
ENST00000616242.5:c.459T= ENSP00000482149.2:p.Pro153=
ENST00000682635.1:n.945T=
ENST00000345378.7:c.462T= ENSP00000223366.2:p.Pro154=
ENST00000403799.8:c.459T= MANE Select ENSP00000384247.3:p.Pro153=
ENST00000671824.1:c.459T= ENSP00000500264.1:p.Pro153=
ENST00000673284.1:c.459T= ENSP00000499852.1:p.Pro153=
ENST00000345378.6:c.462T= ENSP00000223366.2:p.Pro154=
ENST00000395796.7:c.456T= ENSP00000379142.3:p.Pro152=
ENST00000403799.7:c.459T= ENSP00000384247.3:p.Pro153=
ENST00000437084.1:c.408T= ENSP00000402840.1:p.Pro136=
ENST00000616242.4:c.456T= ENSP00000482149.1:p.Pro152=
NM_000162.3:c.459T= NP_000153.1:p.Pro153=
NM_033507.1:c.462T= NP_277042.1:p.Pro154=
NM_033508.1:c.456T= NP_277043.1:p.Pro152=
NM_000162.4:c.459T= NP_000153.1:p.Pro153=
NM_001354800.1:c.459T= NP_001341729.1:p.Pro153=
NM_033507.2:c.462T= NP_277042.1:p.Pro154=
NM_033508.2:c.456T= NP_277043.1:p.Pro152=
NM_000162.5:c.459T= MANE Select NP_000153.1:p.Pro153=
NM_033507.3:c.462T= NP_277042.1:p.Pro154=
NM_033508.3:c.456T= NP_277043.1:p.Pro152=
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