Canonical Allele Identifier: CA2695203022
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44153378_44153383del , CM000669.2:g.44153378_44153383del GRCh38
NC_000007.13:g.44192977_44192982del , CM000669.1:g.44192977_44192982del GRCh37
NC_000007.12:g.44159502_44159507del NCBI36
NG_008847.1:g.41043_41048del
NG_008847.2:g.49790_49795del

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*126_*131del ENSP00000379142.4:n.*126_*131del
ENST00000616242.5:c.128_133del ENSP00000482149.2:p.Arg43_Gly44del
ENST00000682635.1:n.614_619del
ENST00000345378.7:c.131_136del ENSP00000223366.2:p.Arg44_Gly45del
ENST00000403799.8:c.128_133del MANE Select ENSP00000384247.3:p.Arg43_Gly44del
ENST00000671824.1:c.128_133del ENSP00000500264.1:p.Arg43_Gly44del
ENST00000673284.1:c.128_133del ENSP00000499852.1:p.Arg43_Gly44del
ENST00000345378.6:c.131_136del ENSP00000223366.2:p.Arg44_Gly45del
ENST00000395796.7:c.125_130del ENSP00000379142.3:p.Arg42_Gly43del
ENST00000403799.7:c.128_133del ENSP00000384247.3:p.Arg43_Gly44del
ENST00000437084.1:c.128_133del ENSP00000402840.1:p.Arg43_Gly44del
ENST00000616242.4:c.125_130del ENSP00000482149.1:p.Arg42_Gly43del
NM_000162.3:c.128_133del NP_000153.1:p.Arg43_Gly44del
NM_033507.1:c.131_136del NP_277042.1:p.Arg44_Gly45del
NM_033508.1:c.125_130del NP_277043.1:p.Arg42_Gly43del
NM_000162.4:c.128_133del NP_000153.1:p.Arg43_Gly44del
NM_001354800.1:c.128_133del NP_001341729.1:p.Arg43_Gly44del
NM_033507.2:c.131_136del NP_277042.1:p.Arg44_Gly45del
NM_033508.2:c.125_130del NP_277043.1:p.Arg42_Gly43del
NM_000162.5:c.128_133del MANE Select NP_000153.1:p.Arg43_Gly44del
NM_033507.3:c.131_136del NP_277042.1:p.Arg44_Gly45del
NM_033508.3:c.125_130del NP_277043.1:p.Arg42_Gly43del