Canonical Allele Identifier: CA1703635614
Gene: GCK HGNC NCBI

Linked Data

dbSNP Id: rs2096277598

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44149239_44149243del , CM000669.2:g.44149239_44149243del GRCh38
NC_000007.13:g.44188838_44188842del , CM000669.1:g.44188838_44188842del GRCh37
NC_000007.12:g.44155363_44155367del NCBI36
NG_008847.1:g.45186_45190del
NG_008847.2:g.53933_53937del

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*677+522_*677+526del ENSP00000379142.4:n.*677+522_*677+526del
ENST00000616242.5:c.679+522_679+526del ENSP00000482149.2:n.679+522_679+526del
ENST00000682635.1:n.1687_1691del
ENST00000345378.7:c.682+522_682+526del ENSP00000223366.2:n.682+522_682+526del
ENST00000403799.8:c.679+522_679+526del MANE Select ENSP00000384247.3:n.679+522_679+526del
ENST00000671824.1:c.679+522_679+526del ENSP00000500264.1:n.679+522_679+526del
ENST00000673284.1:c.679+522_679+526del ENSP00000499852.1:n.679+522_679+526del
ENST00000345378.6:c.682+522_682+526del ENSP00000223366.2:n.682+522_682+526del
ENST00000395796.7:c.676+522_676+526del ENSP00000379142.3:n.676+522_676+526del
ENST00000403799.7:c.679+522_679+526del ENSP00000384247.3:n.679+522_679+526del
ENST00000437084.1:c.628+522_628+526del ENSP00000402840.1:n.628+522_628+526del
ENST00000616242.4:c.676+522_676+526del ENSP00000482149.1:n.676+522_676+526del
NM_000162.3:c.679+522_679+526del NP_000153.1:n.679+522_679+526del
NM_033507.1:c.682+522_682+526del NP_277042.1:n.682+522_682+526del
NM_033508.1:c.676+522_676+526del NP_277043.1:n.676+522_676+526del
XR_927223.1:n.151_155del
NM_000162.4:c.679+522_679+526del NP_000153.1:n.679+522_679+526del
NM_001354800.1:c.679+522_679+526del NP_001341729.1:n.679+522_679+526del
NM_033507.2:c.682+522_682+526del NP_277042.1:n.682+522_682+526del
NM_033508.2:c.676+522_676+526del NP_277043.1:n.676+522_676+526del
XR_927223.2:n.151_155del
NM_000162.5:c.679+522_679+526del MANE Select NP_000153.1:n.679+522_679+526del
NM_033507.3:c.682+522_682+526del NP_277042.1:n.682+522_682+526del
NM_033508.3:c.676+522_676+526del NP_277043.1:n.676+522_676+526del