Canonical Allele Identifier: CA2775231328
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44150224_44150225del , CM000669.2:g.44150224_44150225del GRCh38
NC_000007.13:g.44189823_44189824del , CM000669.1:g.44189823_44189824del GRCh37
NC_000007.12:g.44156348_44156349del NCBI36
NG_008847.1:g.44199_44200del
NG_008847.2:g.52946_52947del

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*482-161_*482-160del ENSP00000379142.4:n.*482-161_*482-160del
ENST00000616242.5:c.484-161_484-160del ENSP00000482149.2:n.484-161_484-160del
ENST00000682635.1:n.970-161_970-160del
ENST00000345378.7:c.487-161_487-160del ENSP00000223366.2:n.487-161_487-160del
ENST00000403799.8:c.484-161_484-160del MANE Select ENSP00000384247.3:n.484-161_484-160del
ENST00000671824.1:c.484-161_484-160del ENSP00000500264.1:n.484-161_484-160del
ENST00000673284.1:c.484-161_484-160del ENSP00000499852.1:n.484-161_484-160del
ENST00000345378.6:c.487-161_487-160del ENSP00000223366.2:n.487-161_487-160del
ENST00000395796.7:c.481-161_481-160del ENSP00000379142.3:n.481-161_481-160del
ENST00000403799.7:c.484-161_484-160del ENSP00000384247.3:n.484-161_484-160del
ENST00000437084.1:c.433-161_433-160del ENSP00000402840.1:n.433-161_433-160del
ENST00000616242.4:c.481-161_481-160del ENSP00000482149.1:n.481-161_481-160del
NM_000162.3:c.484-161_484-160del NP_000153.1:n.484-161_484-160del
NM_033507.1:c.487-161_487-160del NP_277042.1:n.487-161_487-160del
NM_033508.1:c.481-161_481-160del NP_277043.1:n.481-161_481-160del
NM_000162.4:c.484-161_484-160del NP_000153.1:n.484-161_484-160del
NM_001354800.1:c.484-161_484-160del NP_001341729.1:n.484-161_484-160del
NM_033507.2:c.487-161_487-160del NP_277042.1:n.487-161_487-160del
NM_033508.2:c.481-161_481-160del NP_277043.1:n.481-161_481-160del
NM_000162.5:c.484-161_484-160del MANE Select NP_000153.1:n.484-161_484-160del
NM_033507.3:c.487-161_487-160del NP_277042.1:n.487-161_487-160del
NM_033508.3:c.481-161_481-160del NP_277043.1:n.481-161_481-160del