Canonical Allele Identifier: CA4239557
Gene: GCK HGNC NCBI

Linked Data

dbSNP Id: rs767182194

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44149726del , CM000669.2:g.44149726del GRCh38
NC_000007.13:g.44189325del , CM000669.1:g.44189325del GRCh37
NC_000007.12:g.44155850del NCBI36
NG_008847.1:g.44698del
NG_008847.2:g.53445del

Transcript Alleles

HGVS Amino-acid change
ENST00000395796.8:c.*677+34del ENSP00000379142.4:n.*677+34del
ENST00000616242.5:c.679+34del ENSP00000482149.2:n.679+34del
ENST00000682635.1:n.1199del
ENST00000345378.7:c.682+34del ENSP00000223366.2:n.682+34del
ENST00000403799.8:c.679+34del MANE Select ENSP00000384247.3:n.679+34del
ENST00000671824.1:c.679+34del ENSP00000500264.1:n.679+34del
ENST00000673284.1:c.679+34del ENSP00000499852.1:n.679+34del
ENST00000345378.6:c.682+34del ENSP00000223366.2:n.682+34del
ENST00000395796.7:c.676+34del ENSP00000379142.3:n.676+34del
ENST00000403799.7:c.679+34del ENSP00000384247.3:n.679+34del
ENST00000437084.1:c.628+34del ENSP00000402840.1:n.628+34del
ENST00000616242.4:n.676+34del ENSP00000482149.1:n.676+34del
NM_000162.3:c.679+34del NP_000153.1:n.679+34del
NM_033507.1:c.682+34del NP_277042.1:n.682+34del
NM_033508.1:c.676+34del NP_277043.1:n.676+34del
XR_927223.1:n.241del
NM_000162.4:c.679+34del NP_000153.1:n.679+34del
NM_001354800.1:c.679+34del NP_001341729.1:n.679+34del
NM_033507.2:c.682+34del NP_277042.1:n.682+34del
NM_033508.2:c.676+34del NP_277043.1:n.676+34del
XR_927223.2:n.241del
NM_000162.5:c.679+34del MANE Select NP_000153.1:n.679+34del
NM_033507.3:c.682+34del NP_277042.1:n.682+34del
NM_033508.3:c.676+34del NP_277043.1:n.676+34del