Canonical Allele Identifier: CA574226482
Gene: GCK HGNC NCBI

Linked Data

dbSNP Id: rs1562719948

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44153500_44153501insTCCCCACACCATCCCACTGCCTTGATTCACACCCAGCCCACAGAC , CM000669.2:g.44153500_44153501insTCCCCACACCATCCCACTGCCTTGATTCACACCCAGCCCACAGAC GRCh38
NC_000007.13:g.44193099_44193100insTCCCCACACCATCCCACTGCCTTGATTCACACCCAGCCCACAGAC , CM000669.1:g.44193099_44193100insTCCCCACACCATCCCACTGCCTTGATTCACACCCAGCCCACAGAC GRCh37
NC_000007.12:g.44159624_44159625insTCCCCACACCATCCCACTGCCTTGATTCACACCCAGCCCACAGAC NCBI36
NG_008847.1:g.40923_40924insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA
NG_008847.2:g.49670_49671insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*44-38_*44-37insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA ENSP00000379142.4:n.*44-38_*44-37insGTCTGTGGGCTGGGTGTGAATCAAG...
ENST00000616242.5:c.46-38_46-37insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA ENSP00000482149.2:n.46-38_46-37insGTCTGTGGGCTGGGTGTGAATCAAGGC...
ENST00000682635.1:n.532-38_532-37insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA
ENST00000345378.7:c.49-38_49-37insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA ENSP00000223366.2:n.49-38_49-37insGTCTGTGGGCTGGGTGTGAATCAAGGC...
ENST00000403799.8:c.46-38_46-37insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA MANE Select ENSP00000384247.3:n.46-38_46-37insGTCTGTGGGCTGGGTGTGAATCAAGGC...
ENST00000671824.1:c.46-38_46-37insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA ENSP00000500264.1:n.46-38_46-37insGTCTGTGGGCTGGGTGTGAATCAAGGC...
ENST00000673284.1:c.46-38_46-37insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA ENSP00000499852.1:n.46-38_46-37insGTCTGTGGGCTGGGTGTGAATCAAGGC...
ENST00000345378.6:c.49-38_49-37insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA ENSP00000223366.2:n.49-38_49-37insGTCTGTGGGCTGGGTGTGAATCAAGGC...
ENST00000395796.7:c.43-38_43-37insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA ENSP00000379142.3:n.43-38_43-37insGTCTGTGGGCTGGGTGTGAATCAAGGC...
ENST00000403799.7:c.46-38_46-37insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA ENSP00000384247.3:n.46-38_46-37insGTCTGTGGGCTGGGTGTGAATCAAGGC...
ENST00000437084.1:c.46-38_46-37insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA ENSP00000402840.1:n.46-38_46-37insGTCTGTGGGCTGGGTGTGAATCAAGGC...
ENST00000476008.1:n.481-38_481-37insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA
ENST00000616242.4:c.43-38_43-37insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA ENSP00000482149.1:n.43-38_43-37insGTCTGTGGGCTGGGTGTGAATCAAGGC...
NM_000162.3:c.46-38_46-37insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA NP_000153.1:n.46-38_46-37insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGG...
NM_033507.1:c.49-38_49-37insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA NP_277042.1:n.49-38_49-37insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGG...
NM_033508.1:c.43-38_43-37insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA NP_277043.1:n.43-38_43-37insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGG...
NM_000162.4:c.46-38_46-37insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA NP_000153.1:n.46-38_46-37insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGG...
NM_001354800.1:c.46-38_46-37insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA NP_001341729.1:n.46-38_46-37insGTCTGTGGGCTGGGTGTGAATCAAGGCAGT...
NM_033507.2:c.49-38_49-37insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA NP_277042.1:n.49-38_49-37insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGG...
NM_033508.2:c.43-38_43-37insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA NP_277043.1:n.43-38_43-37insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGG...
NM_000162.5:c.46-38_46-37insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA MANE Select NP_000153.1:n.46-38_46-37insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGG...
NM_033507.3:c.49-38_49-37insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA NP_277042.1:n.49-38_49-37insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGG...
NM_033508.3:c.43-38_43-37insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA NP_277043.1:n.43-38_43-37insGTCTGTGGGCTGGGTGTGAATCAAGGCAGTGGG...