Canonical Allele Identifier: CA2838644112

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44153506_44153507insGCAGTGGGGGGGGGGGGGGGG , CM000669.2:g.44153506_44153507insGCAGTGGGGGGGGGGGGGGGG	GRCh38
NC_000007.13:g.44193105_44193106insGCAGTGGGGGGGGGGGGGGGG , CM000669.1:g.44193105_44193106insGCAGTGGGGGGGGGGGGGGGG	GRCh37
NC_000007.12:g.44159630_44159631insGCAGTGGGGGGGGGGGGGGGG	NCBI36
NG_008847.1:g.40922_40923insCCCCCCCCCCCACTGCCCCCC
NG_008847.2:g.49669_49670insCCCCCCCCCCCACTGCCCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*44-39_*44-38insCCCCCCCCCCCACTGCCCCCC	ENSP00000379142.4:n.*44-39_*44-38insCCCCCCCCCCCACTGCCCCCC
ENST00000616242.5:c.46-39_46-38insCCCCCCCCCCCACTGCCCCCC	ENSP00000482149.2:n.46-39_46-38insCCCCCCCCCCCACTGCCCCCC
ENST00000682635.1:n.532-39_532-38insCCCCCCCCCCCACTGCCCCCC
ENST00000345378.7:c.49-39_49-38insCCCCCCCCCCCACTGCCCCCC	ENSP00000223366.2:n.49-39_49-38insCCCCCCCCCCCACTGCCCCCC
ENST00000403799.8:c.46-39_46-38insCCCCCCCCCCCACTGCCCCCC MANE Select	ENSP00000384247.3:n.46-39_46-38insCCCCCCCCCCCACTGCCCCCC
ENST00000671824.1:c.46-39_46-38insCCCCCCCCCCCACTGCCCCCC	ENSP00000500264.1:n.46-39_46-38insCCCCCCCCCCCACTGCCCCCC
ENST00000673284.1:c.46-39_46-38insCCCCCCCCCCCACTGCCCCCC	ENSP00000499852.1:n.46-39_46-38insCCCCCCCCCCCACTGCCCCCC
ENST00000345378.6:c.49-39_49-38insCCCCCCCCCCCACTGCCCCCC	ENSP00000223366.2:n.49-39_49-38insCCCCCCCCCCCACTGCCCCCC
ENST00000395796.7:c.43-39_43-38insCCCCCCCCCCCACTGCCCCCC	ENSP00000379142.3:n.43-39_43-38insCCCCCCCCCCCACTGCCCCCC
ENST00000403799.7:c.46-39_46-38insCCCCCCCCCCCACTGCCCCCC	ENSP00000384247.3:n.46-39_46-38insCCCCCCCCCCCACTGCCCCCC
ENST00000437084.1:c.46-39_46-38insCCCCCCCCCCCACTGCCCCCC	ENSP00000402840.1:n.46-39_46-38insCCCCCCCCCCCACTGCCCCCC
ENST00000476008.1:n.481-39_481-38insCCCCCCCCCCCACTGCCCCCC
ENST00000616242.4:c.43-39_43-38insCCCCCCCCCCCACTGCCCCCC	ENSP00000482149.1:n.43-39_43-38insCCCCCCCCCCCACTGCCCCCC
NM_000162.3:c.46-39_46-38insCCCCCCCCCCCACTGCCCCCC	NP_000153.1:n.46-39_46-38insCCCCCCCCCCCACTGCCCCCC
NM_033507.1:c.49-39_49-38insCCCCCCCCCCCACTGCCCCCC	NP_277042.1:n.49-39_49-38insCCCCCCCCCCCACTGCCCCCC
NM_033508.1:c.43-39_43-38insCCCCCCCCCCCACTGCCCCCC	NP_277043.1:n.43-39_43-38insCCCCCCCCCCCACTGCCCCCC
NM_000162.4:c.46-39_46-38insCCCCCCCCCCCACTGCCCCCC	NP_000153.1:n.46-39_46-38insCCCCCCCCCCCACTGCCCCCC
NM_001354800.1:c.46-39_46-38insCCCCCCCCCCCACTGCCCCCC	NP_001341729.1:n.46-39_46-38insCCCCCCCCCCCACTGCCCCCC
NM_033507.2:c.49-39_49-38insCCCCCCCCCCCACTGCCCCCC	NP_277042.1:n.49-39_49-38insCCCCCCCCCCCACTGCCCCCC
NM_033508.2:c.43-39_43-38insCCCCCCCCCCCACTGCCCCCC	NP_277043.1:n.43-39_43-38insCCCCCCCCCCCACTGCCCCCC
NM_000162.5:c.46-39_46-38insCCCCCCCCCCCACTGCCCCCC MANE Select	NP_000153.1:n.46-39_46-38insCCCCCCCCCCCACTGCCCCCC
NM_033507.3:c.49-39_49-38insCCCCCCCCCCCACTGCCCCCC	NP_277042.1:n.49-39_49-38insCCCCCCCCCCCACTGCCCCCC
NM_033508.3:c.43-39_43-38insCCCCCCCCCCCACTGCCCCCC	NP_277043.1:n.43-39_43-38insCCCCCCCCCCCACTGCCCCCC