Canonical Allele Identifier: CA1703636478
Gene: GCK HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44151052G= , CM000669.2:g.44151052G= GRCh38
NC_000007.13:g.44190651G= , CM000669.1:g.44190651G= GRCh37
NC_000007.12:g.44157176G= NCBI36
NG_008847.1:g.43372C=
NG_008847.2:g.52119C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*385C= ENSP00000379142.4:n.*385C=
ENST00000616242.5:c.387C= ENSP00000482149.2:p.Cys129=
ENST00000682635.1:n.873C=
ENST00000345378.7:c.390C= ENSP00000223366.2:p.Cys130=
ENST00000403799.8:c.387C= MANE Select ENSP00000384247.3:p.Cys129=
ENST00000671824.1:c.387C= ENSP00000500264.1:p.Cys129=
ENST00000673284.1:c.387C= ENSP00000499852.1:p.Cys129=
ENST00000345378.6:c.390C= ENSP00000223366.2:p.Cys130=
ENST00000395796.7:c.384C= ENSP00000379142.3:p.Cys128=
ENST00000403799.7:c.387C= ENSP00000384247.3:p.Cys129=
ENST00000437084.1:c.364-28C= ENSP00000402840.1:n.364-28C=
ENST00000616242.4:c.384C= ENSP00000482149.1:p.Cys128=
NM_000162.3:c.387C= NP_000153.1:p.Cys129=
NM_033507.1:c.390C= NP_277042.1:p.Cys130=
NM_033508.1:c.384C= NP_277043.1:p.Cys128=
NM_000162.4:c.387C= NP_000153.1:p.Cys129=
NM_001354800.1:c.387C= NP_001341729.1:p.Cys129=
NM_033507.2:c.390C= NP_277042.1:p.Cys130=
NM_033508.2:c.384C= NP_277043.1:p.Cys128=
NM_000162.5:c.387C= MANE Select NP_000153.1:p.Cys129=
NM_033507.3:c.390C= NP_277042.1:p.Cys130=
NM_033508.3:c.384C= NP_277043.1:p.Cys128=
Search 100 bp 5'
Search 100 bp 3'