Canonical Allele Identifier: CA1703636496
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44151092_44151121delinsATGGTGACCATCTGGCATGGGGGGGTGCGC , CM000669.2:g.44151092_44151121delinsATGGTGACCATCTGGCATGGGGGGGTGCGC GRCh38
NC_000007.13:g.44190691_44190720delinsATGGTGACCATCTGGCATGGGGGGGTGCGC , CM000669.1:g.44190691_44190720delinsATGGTGACCATCTGGCATGGGGGGGTGCGC GRCh37
NC_000007.12:g.44157216_44157245delinsATGGTGACCATCTGGCATGGGGGGGTGCGC NCBI36
NG_008847.1:g.43303_43332delinsGCGCACCCCCCCATGCCAGATGGTCACCAT
NG_008847.2:g.52050_52079delinsGCGCACCCCCCCATGCCAGATGGTCACCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*362-46_*362-17delinsGCGCACCCCCCCATGCCAGATGGTCACCAT ENSP00000379142.4:n.*362-46_*362-17delinsGCGCACCCCCCCATGCCAGA...
ENST00000616242.5:c.364-46_364-17delinsGCGCACCCCCCCATGCCAGATGGTCACCAT ENSP00000482149.2:n.364-46_364-17delinsGCGCACCCCCCCATGCCAGATG...
ENST00000682635.1:n.850-46_850-17delinsGCGCACCCCCCCATGCCAGATGGTCACCAT
ENST00000345378.7:c.367-46_367-17delinsGCGCACCCCCCCATGCCAGATGGTCACCAT ENSP00000223366.2:n.367-46_367-17delinsGCGCACCCCCCCATGCCAGATG...
ENST00000403799.8:c.364-46_364-17delinsGCGCACCCCCCCATGCCAGATGGTCACCAT MANE Select ENSP00000384247.3:n.364-46_364-17delinsGCGCACCCCCCCATGCCAGATG...
ENST00000671824.1:c.364-46_364-17delinsGCGCACCCCCCCATGCCAGATGGTCACCAT ENSP00000500264.1:n.364-46_364-17delinsGCGCACCCCCCCATGCCAGATG...
ENST00000673284.1:c.364-46_364-17delinsGCGCACCCCCCCATGCCAGATGGTCACCAT ENSP00000499852.1:n.364-46_364-17delinsGCGCACCCCCCCATGCCAGATG...
ENST00000345378.6:c.367-46_367-17delinsGCGCACCCCCCCATGCCAGATGGTCACCAT ENSP00000223366.2:n.367-46_367-17delinsGCGCACCCCCCCATGCCAGATG...
ENST00000395796.7:c.361-46_361-17delinsGCGCACCCCCCCATGCCAGATGGTCACCAT ENSP00000379142.3:n.361-46_361-17delinsGCGCACCCCCCCATGCCAGATG...
ENST00000403799.7:c.364-46_364-17delinsGCGCACCCCCCCATGCCAGATGGTCACCAT ENSP00000384247.3:n.364-46_364-17delinsGCGCACCCCCCCATGCCAGATG...
ENST00000437084.1:c.364-97_364-68delinsGCGCACCCCCCCATGCCAGATGGTCACCAT ENSP00000402840.1:n.364-97_364-68delinsGCGCACCCCCCCATGCCAGATG...
ENST00000616242.4:c.361-46_361-17delinsGCGCACCCCCCCATGCCAGATGGTCACCAT ENSP00000482149.1:n.361-46_361-17delinsGCGCACCCCCCCATGCCAGATG...
NM_000162.3:c.364-46_364-17delinsGCGCACCCCCCCATGCCAGATGGTCACCAT NP_000153.1:n.364-46_364-17delinsGCGCACCCCCCCATGCCAGATGGTCACC...
NM_033507.1:c.367-46_367-17delinsGCGCACCCCCCCATGCCAGATGGTCACCAT NP_277042.1:n.367-46_367-17delinsGCGCACCCCCCCATGCCAGATGGTCACC...
NM_033508.1:c.361-46_361-17delinsGCGCACCCCCCCATGCCAGATGGTCACCAT NP_277043.1:n.361-46_361-17delinsGCGCACCCCCCCATGCCAGATGGTCACC...
NM_000162.4:c.364-46_364-17delinsGCGCACCCCCCCATGCCAGATGGTCACCAT NP_000153.1:n.364-46_364-17delinsGCGCACCCCCCCATGCCAGATGGTCACC...
NM_001354800.1:c.364-46_364-17delinsGCGCACCCCCCCATGCCAGATGGTCACCAT NP_001341729.1:n.364-46_364-17delinsGCGCACCCCCCCATGCCAGATGGTC...
NM_033507.2:c.367-46_367-17delinsGCGCACCCCCCCATGCCAGATGGTCACCAT NP_277042.1:n.367-46_367-17delinsGCGCACCCCCCCATGCCAGATGGTCACC...
NM_033508.2:c.361-46_361-17delinsGCGCACCCCCCCATGCCAGATGGTCACCAT NP_277043.1:n.361-46_361-17delinsGCGCACCCCCCCATGCCAGATGGTCACC...
NM_000162.5:c.364-46_364-17delinsGCGCACCCCCCCATGCCAGATGGTCACCAT MANE Select NP_000153.1:n.364-46_364-17delinsGCGCACCCCCCCATGCCAGATGGTCACC...
NM_033507.3:c.367-46_367-17delinsGCGCACCCCCCCATGCCAGATGGTCACCAT NP_277042.1:n.367-46_367-17delinsGCGCACCCCCCCATGCCAGATGGTCACC...
NM_033508.3:c.361-46_361-17delinsGCGCACCCCCCCATGCCAGATGGTCACCAT NP_277043.1:n.361-46_361-17delinsGCGCACCCCCCCATGCCAGATGGTCACC...