Canonical Allele Identifier: CA573797938
Gene: GCK HGNC NCBI

Linked Data

dbSNP Id: rs1562717487

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44150101_44150102del , CM000669.2:g.44150101_44150102del GRCh38
NC_000007.13:g.44189700_44189701del , CM000669.1:g.44189700_44189701del GRCh37
NC_000007.12:g.44156225_44156226del NCBI36
NG_008847.1:g.44325_44326del
NG_008847.2:g.53072_53073del

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*482-35_*482-34del ENSP00000379142.4:n.*482-35_*482-34del
ENST00000616242.5:c.484-35_484-34del ENSP00000482149.2:n.484-35_484-34del
ENST00000682635.1:n.970-35_970-34del
ENST00000345378.7:c.487-35_487-34del ENSP00000223366.2:n.487-35_487-34del
ENST00000403799.8:c.484-35_484-34del MANE Select ENSP00000384247.3:n.484-35_484-34del
ENST00000671824.1:c.484-35_484-34del ENSP00000500264.1:n.484-35_484-34del
ENST00000673284.1:c.484-35_484-34del ENSP00000499852.1:n.484-35_484-34del
ENST00000345378.6:c.487-35_487-34del ENSP00000223366.2:n.487-35_487-34del
ENST00000395796.7:c.481-35_481-34del ENSP00000379142.3:n.481-35_481-34del
ENST00000403799.7:c.484-35_484-34del ENSP00000384247.3:n.484-35_484-34del
ENST00000437084.1:c.433-35_433-34del ENSP00000402840.1:n.433-35_433-34del
ENST00000616242.4:c.481-35_481-34del ENSP00000482149.1:n.481-35_481-34del
NM_000162.3:c.484-35_484-34del NP_000153.1:n.484-35_484-34del
NM_033507.1:c.487-35_487-34del NP_277042.1:n.487-35_487-34del
NM_033508.1:c.481-35_481-34del NP_277043.1:n.481-35_481-34del
NM_000162.4:c.484-35_484-34del NP_000153.1:n.484-35_484-34del
NM_001354800.1:c.484-35_484-34del NP_001341729.1:n.484-35_484-34del
NM_033507.2:c.487-35_487-34del NP_277042.1:n.487-35_487-34del
NM_033508.2:c.481-35_481-34del NP_277043.1:n.481-35_481-34del
NM_000162.5:c.484-35_484-34del MANE Select NP_000153.1:n.484-35_484-34del
NM_033507.3:c.487-35_487-34del NP_277042.1:n.487-35_487-34del
NM_033508.3:c.481-35_481-34del NP_277043.1:n.481-35_481-34del