Canonical Allele Identifier: CA1703635826
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44149725_44149726delinsAG , CM000669.2:g.44149725_44149726delinsAG GRCh38
NC_000007.13:g.44189324_44189325delinsAG , CM000669.1:g.44189324_44189325delinsAG GRCh37
NC_000007.12:g.44155849_44155850delinsAG NCBI36
NG_008847.1:g.44698_44699delinsCT
NG_008847.2:g.53445_53446delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000395796.8:c.*677+34_*677+35delinsCT ENSP00000379142.4:n.*677+34_*677+35delins...
ENST00000616242.5:c.679+34_679+35delinsCT ENSP00000482149.2:n.679+34_679+35delinsCT...
ENST00000682635.1:n.1199_1200delinsCT
ENST00000345378.7:c.682+34_682+35delinsCT ENSP00000223366.2:n.682+34_682+35delinsCT...
ENST00000403799.8:c.679+34_679+35delinsCT MANE Select ENSP00000384247.3:n.679+34_679+35delinsCT...
ENST00000671824.1:c.679+34_679+35delinsCT ENSP00000500264.1:n.679+34_679+35delinsCT...
ENST00000673284.1:c.679+34_679+35delinsCT ENSP00000499852.1:n.679+34_679+35delinsCT...
ENST00000345378.6:c.682+34_682+35delinsCT ENSP00000223366.2:n.682+34_682+35delinsCT...
ENST00000395796.7:c.676+34_676+35delinsCT ENSP00000379142.3:n.676+34_676+35delinsCT...
ENST00000403799.7:c.679+34_679+35delinsCT ENSP00000384247.3:n.679+34_679+35delinsCT...
ENST00000437084.1:c.628+34_628+35delinsCT ENSP00000402840.1:n.628+34_628+35delinsCT...
ENST00000616242.4:n.676+34_676+35delinsCT ENSP00000482149.1:n.676+34_676+35delinsCT...
NM_000162.3:c.679+34_679+35delinsCT NP_000153.1:n.679+34_679+35delinsCT
NM_033507.1:c.682+34_682+35delinsCT NP_277042.1:n.682+34_682+35delinsCT
NM_033508.1:c.676+34_676+35delinsCT NP_277043.1:n.676+34_676+35delinsCT
XR_927223.1:n.240_241delinsAG
NM_000162.4:c.679+34_679+35delinsCT NP_000153.1:n.679+34_679+35delinsCT
NM_001354800.1:c.679+34_679+35delinsCT NP_001341729.1:n.679+34_679+35delinsCT
NM_033507.2:c.682+34_682+35delinsCT NP_277042.1:n.682+34_682+35delinsCT
NM_033508.2:c.676+34_676+35delinsCT NP_277043.1:n.676+34_676+35delinsCT
XR_927223.2:n.240_241delinsAG
NM_000162.5:c.679+34_679+35delinsCT MANE Select NP_000153.1:n.679+34_679+35delinsCT
NM_033507.3:c.682+34_682+35delinsCT NP_277042.1:n.682+34_682+35delinsCT
NM_033508.3:c.676+34_676+35delinsCT NP_277043.1:n.676+34_676+35delinsCT