Canonical Allele Identifier: CA157917712
Gene: GCK HGNC NCBI

Linked Data

dbSNP Id: rs752910444

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44150208_44150209del , CM000669.2:g.44150208_44150209del GRCh38
NC_000007.13:g.44189807_44189808del , CM000669.1:g.44189807_44189808del GRCh37
NC_000007.12:g.44156332_44156333del NCBI36
NG_008847.1:g.44216_44217del
NG_008847.2:g.52963_52964del

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*482-144_*482-143del ENSP00000379142.4:n.*482-144_*482-143del
ENST00000616242.5:c.484-144_484-143del ENSP00000482149.2:n.484-144_484-143del
ENST00000682635.1:n.970-144_970-143del
ENST00000345378.7:c.487-144_487-143del ENSP00000223366.2:n.487-144_487-143del
ENST00000403799.8:c.484-144_484-143del MANE Select ENSP00000384247.3:n.484-144_484-143del
ENST00000671824.1:c.484-144_484-143del ENSP00000500264.1:n.484-144_484-143del
ENST00000673284.1:c.484-144_484-143del ENSP00000499852.1:n.484-144_484-143del
ENST00000345378.6:c.487-144_487-143del ENSP00000223366.2:n.487-144_487-143del
ENST00000395796.7:c.481-144_481-143del ENSP00000379142.3:n.481-144_481-143del
ENST00000403799.7:c.484-144_484-143del ENSP00000384247.3:n.484-144_484-143del
ENST00000437084.1:c.433-144_433-143del ENSP00000402840.1:n.433-144_433-143del
ENST00000616242.4:c.481-144_481-143del ENSP00000482149.1:n.481-144_481-143del
NM_000162.3:c.484-144_484-143del NP_000153.1:n.484-144_484-143del
NM_033507.1:c.487-144_487-143del NP_277042.1:n.487-144_487-143del
NM_033508.1:c.481-144_481-143del NP_277043.1:n.481-144_481-143del
NM_000162.4:c.484-144_484-143del NP_000153.1:n.484-144_484-143del
NM_001354800.1:c.484-144_484-143del NP_001341729.1:n.484-144_484-143del
NM_033507.2:c.487-144_487-143del NP_277042.1:n.487-144_487-143del
NM_033508.2:c.481-144_481-143del NP_277043.1:n.481-144_481-143del
NM_000162.5:c.484-144_484-143del MANE Select NP_000153.1:n.484-144_484-143del
NM_033507.3:c.487-144_487-143del NP_277042.1:n.487-144_487-143del
NM_033508.3:c.481-144_481-143del NP_277043.1:n.481-144_481-143del