Canonical Allele Identifier: CA1703635993
Gene: GCK HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44150045G= , CM000669.2:g.44150045G= GRCh38
NC_000007.13:g.44189644G= , CM000669.1:g.44189644G= GRCh37
NC_000007.12:g.44156169G= NCBI36
NG_008847.1:g.44379C=
NG_008847.2:g.53126C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*501C= ENSP00000379142.4:n.*501C=
ENST00000616242.5:c.503C= ENSP00000482149.2:p.Thr168=
ENST00000682635.1:n.989C=
ENST00000345378.7:c.506C= ENSP00000223366.2:p.Thr169=
ENST00000403799.8:c.503C= MANE Select ENSP00000384247.3:p.Thr168=
ENST00000671824.1:c.503C= ENSP00000500264.1:p.Thr168=
ENST00000673284.1:c.503C= ENSP00000499852.1:p.Thr168=
ENST00000345378.6:c.506C= ENSP00000223366.2:p.Thr169=
ENST00000395796.7:c.500C= ENSP00000379142.3:p.Thr167=
ENST00000403799.7:c.503C= ENSP00000384247.3:p.Thr168=
ENST00000437084.1:c.452C= ENSP00000402840.1:p.Thr151=
ENST00000616242.4:c.500C= ENSP00000482149.1:p.Thr167=
NM_000162.3:c.503C= NP_000153.1:p.Thr168=
NM_033507.1:c.506C= NP_277042.1:p.Thr169=
NM_033508.1:c.500C= NP_277043.1:p.Thr167=
NM_000162.4:c.503C= NP_000153.1:p.Thr168=
NM_001354800.1:c.503C= NP_001341729.1:p.Thr168=
NM_033507.2:c.506C= NP_277042.1:p.Thr169=
NM_033508.2:c.500C= NP_277043.1:p.Thr167=
NM_000162.5:c.503C= MANE Select NP_000153.1:p.Thr168=
NM_033507.3:c.506C= NP_277042.1:p.Thr169=
NM_033508.3:c.500C= NP_277043.1:p.Thr167=
Search 100 bp 5'
Search 100 bp 3'