Canonical Allele Identifier: CA1703635543
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44149107_44149108delinsCA , CM000669.2:g.44149107_44149108delinsCA GRCh38
NC_000007.13:g.44188706_44188707delinsCA , CM000669.1:g.44188706_44188707delinsCA GRCh37
NC_000007.12:g.44155231_44155232delinsCA NCBI36
NG_008847.1:g.45316_45317delinsTG
NG_008847.2:g.54063_54064delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*677+652_*677+653delinsTG ENSP00000379142.4:n.*677+652_*677+653delinsTG
ENST00000616242.5:c.679+652_679+653delinsTG ENSP00000482149.2:n.679+652_679+653delinsTG
ENST00000682635.1:n.1817_1818delinsTG
ENST00000345378.7:c.682+652_682+653delinsTG ENSP00000223366.2:n.682+652_682+653delinsTG
ENST00000403799.8:c.679+652_679+653delinsTG MANE Select ENSP00000384247.3:n.679+652_679+653delinsTG
ENST00000671824.1:c.679+652_679+653delinsTG ENSP00000500264.1:n.679+652_679+653delinsTG
ENST00000673284.1:c.679+652_679+653delinsTG ENSP00000499852.1:n.679+652_679+653delinsTG
ENST00000345378.6:c.682+652_682+653delinsTG ENSP00000223366.2:n.682+652_682+653delinsTG
ENST00000395796.7:c.676+652_676+653delinsTG ENSP00000379142.3:n.676+652_676+653delinsTG
ENST00000403799.7:c.679+652_679+653delinsTG ENSP00000384247.3:n.679+652_679+653delinsTG
ENST00000437084.1:c.628+652_628+653delinsTG ENSP00000402840.1:n.628+652_628+653delinsTG
ENST00000616242.4:c.676+652_676+653delinsTG ENSP00000482149.1:n.676+652_676+653delinsTG
NM_000162.3:c.679+652_679+653delinsTG NP_000153.1:n.679+652_679+653delinsTG
NM_033507.1:c.682+652_682+653delinsTG NP_277042.1:n.682+652_682+653delinsTG
NM_033508.1:c.676+652_676+653delinsTG NP_277043.1:n.676+652_676+653delinsTG
XR_927223.1:n.83-64_83-63delinsCA
NM_000162.4:c.679+652_679+653delinsTG NP_000153.1:n.679+652_679+653delinsTG
NM_001354800.1:c.679+652_679+653delinsTG NP_001341729.1:n.679+652_679+653delinsTG
NM_033507.2:c.682+652_682+653delinsTG NP_277042.1:n.682+652_682+653delinsTG
NM_033508.2:c.676+652_676+653delinsTG NP_277043.1:n.676+652_676+653delinsTG
XR_927223.2:n.83-64_83-63delinsCA
NM_000162.5:c.679+652_679+653delinsTG MANE Select NP_000153.1:n.679+652_679+653delinsTG
NM_033507.3:c.682+652_682+653delinsTG NP_277042.1:n.682+652_682+653delinsTG
NM_033508.3:c.676+652_676+653delinsTG NP_277043.1:n.676+652_676+653delinsTG