Canonical Allele Identifier: CA1703636445
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44150979C= , CM000669.2:g.44150979C= GRCh38
NC_000007.13:g.44190578C= , CM000669.1:g.44190578C= GRCh37
NC_000007.12:g.44157103C= NCBI36
NG_008847.1:g.43445G=
NG_008847.2:g.52192G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*458G= ENSP00000379142.4:n.*458G=
ENST00000616242.5:c.460G= ENSP00000482149.2:p.Val154=
ENST00000682635.1:n.946G=
ENST00000345378.7:c.463G= ENSP00000223366.2:p.Val155=
ENST00000403799.8:c.460G= MANE Select ENSP00000384247.3:p.Val154=
ENST00000671824.1:c.460G= ENSP00000500264.1:p.Val154=
ENST00000673284.1:c.460G= ENSP00000499852.1:p.Val154=
ENST00000345378.6:c.463G= ENSP00000223366.2:p.Val155=
ENST00000395796.7:c.457G= ENSP00000379142.3:p.Val153=
ENST00000403799.7:c.460G= ENSP00000384247.3:p.Val154=
ENST00000437084.1:c.409G= ENSP00000402840.1:p.Val137=
ENST00000616242.4:c.457G= ENSP00000482149.1:p.Val153=
NM_000162.3:c.460G= NP_000153.1:p.Val154=
NM_033507.1:c.463G= NP_277042.1:p.Val155=
NM_033508.1:c.457G= NP_277043.1:p.Val153=
NM_000162.4:c.460G= NP_000153.1:p.Val154=
NM_001354800.1:c.460G= NP_001341729.1:p.Val154=
NM_033507.2:c.463G= NP_277042.1:p.Val155=
NM_033508.2:c.457G= NP_277043.1:p.Val153=
NM_000162.5:c.460G= MANE Select NP_000153.1:p.Val154=
NM_033507.3:c.463G= NP_277042.1:p.Val155=
NM_033508.3:c.457G= NP_277043.1:p.Val153=
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