Canonical Allele Identifier: CA1703635855
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44149772C= , CM000669.2:g.44149772C= GRCh38
NC_000007.13:g.44189371C= , CM000669.1:g.44189371C= GRCh37
NC_000007.12:g.44155896C= NCBI36
NG_008847.1:g.44652G=
NG_008847.2:g.53399G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*665G= ENSP00000379142.4:n.*665G=
ENST00000616242.5:c.667G= ENSP00000482149.2:p.Gly223=
ENST00000682635.1:n.1153G=
ENST00000345378.7:c.670G= ENSP00000223366.2:p.Gly224=
ENST00000403799.8:c.667G= MANE Select ENSP00000384247.3:p.Gly223=
ENST00000671824.1:c.667G= ENSP00000500264.1:p.Gly223=
ENST00000673284.1:c.667G= ENSP00000499852.1:p.Gly223=
ENST00000345378.6:c.670G= ENSP00000223366.2:p.Gly224=
ENST00000395796.7:c.664G= ENSP00000379142.3:p.Gly222=
ENST00000403799.7:c.667G= ENSP00000384247.3:p.Gly223=
ENST00000437084.1:c.616G= ENSP00000402840.1:p.Gly206=
ENST00000616242.4:c.664G= ENSP00000482149.1:p.Gly222=
NM_000162.3:c.667G= NP_000153.1:p.Gly223=
NM_033507.1:c.670G= NP_277042.1:p.Gly224=
NM_033508.1:c.664G= NP_277043.1:p.Gly222=
XR_927223.1:n.287C=
NM_000162.4:c.667G= NP_000153.1:p.Gly223=
NM_001354800.1:c.667G= NP_001341729.1:p.Gly223=
NM_033507.2:c.670G= NP_277042.1:p.Gly224=
NM_033508.2:c.664G= NP_277043.1:p.Gly222=
XR_927223.2:n.287C=
NM_000162.5:c.667G= MANE Select NP_000153.1:p.Gly223=
NM_033507.3:c.670G= NP_277042.1:p.Gly224=
NM_033508.3:c.664G= NP_277043.1:p.Gly222=