Canonical Allele Identifier: CA2682576838
Gene: GCK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44153479_44153480del , CM000669.2:g.44153479_44153480del GRCh38
NC_000007.13:g.44193078_44193079del , CM000669.1:g.44193078_44193079del GRCh37
NC_000007.12:g.44159603_44159604del NCBI36
NG_008847.1:g.40944_40945del
NG_008847.2:g.49691_49692del

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*44-17_*44-16del ENSP00000379142.4:n.*44-17_*44-16del
ENST00000616242.5:c.46-17_46-16del ENSP00000482149.2:n.46-17_46-16del
ENST00000682635.1:n.532-17_532-16del
ENST00000345378.7:c.49-17_49-16del ENSP00000223366.2:n.49-17_49-16del
ENST00000403799.8:c.46-17_46-16del MANE Select ENSP00000384247.3:n.46-17_46-16del
ENST00000671824.1:c.46-17_46-16del ENSP00000500264.1:n.46-17_46-16del
ENST00000673284.1:c.46-17_46-16del ENSP00000499852.1:n.46-17_46-16del
ENST00000345378.6:c.49-17_49-16del ENSP00000223366.2:n.49-17_49-16del
ENST00000395796.7:c.43-17_43-16del ENSP00000379142.3:n.43-17_43-16del
ENST00000403799.7:c.46-17_46-16del ENSP00000384247.3:n.46-17_46-16del
ENST00000437084.1:c.46-17_46-16del ENSP00000402840.1:n.46-17_46-16del
ENST00000476008.1:n.481-17_481-16del
ENST00000616242.4:c.43-17_43-16del ENSP00000482149.1:n.43-17_43-16del
NM_000162.3:c.46-17_46-16del NP_000153.1:n.46-17_46-16del
NM_033507.1:c.49-17_49-16del NP_277042.1:n.49-17_49-16del
NM_033508.1:c.43-17_43-16del NP_277043.1:n.43-17_43-16del
NM_000162.4:c.46-17_46-16del NP_000153.1:n.46-17_46-16del
NM_001354800.1:c.46-17_46-16del NP_001341729.1:n.46-17_46-16del
NM_033507.2:c.49-17_49-16del NP_277042.1:n.49-17_49-16del
NM_033508.2:c.43-17_43-16del NP_277043.1:n.43-17_43-16del
NM_000162.5:c.46-17_46-16del MANE Select NP_000153.1:n.46-17_46-16del
NM_033507.3:c.49-17_49-16del NP_277042.1:n.49-17_49-16del
NM_033508.3:c.43-17_43-16del NP_277043.1:n.43-17_43-16del