Canonical Allele Identifier: CA1703635982
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44150018_44150019delinsTC , CM000669.2:g.44150018_44150019delinsTC GRCh38
NC_000007.13:g.44189617_44189618delinsTC , CM000669.1:g.44189617_44189618delinsTC GRCh37
NC_000007.12:g.44156142_44156143delinsTC NCBI36
NG_008847.1:g.44405_44406delinsGA
NG_008847.2:g.53152_53153delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*527_*528delinsGA ENSP00000379142.4:n.*527_*528delinsGA
ENST00000616242.5:c.529_530delinsGA ENSP00000482149.2:p.Glu177=
ENST00000682635.1:n.1015_1016delinsGA
ENST00000345378.7:c.532_533delinsGA ENSP00000223366.2:p.Glu178=
ENST00000403799.8:c.529_530delinsGA MANE Select ENSP00000384247.3:p.Glu177=
ENST00000671824.1:c.529_530delinsGA ENSP00000500264.1:p.Glu177=
ENST00000673284.1:c.529_530delinsGA ENSP00000499852.1:p.Glu177=
ENST00000345378.6:c.532_533delinsGA ENSP00000223366.2:p.Glu178=
ENST00000395796.7:c.526_527delinsGA ENSP00000379142.3:p.Glu176=
ENST00000403799.7:c.529_530delinsGA ENSP00000384247.3:p.Glu177=
ENST00000437084.1:c.478_479delinsGA ENSP00000402840.1:p.Glu160=
ENST00000616242.4:c.526_527delinsGA ENSP00000482149.1:p.Glu176=
NM_000162.3:c.529_530delinsGA NP_000153.1:p.Glu177=
NM_033507.1:c.532_533delinsGA NP_277042.1:p.Glu178=
NM_033508.1:c.526_527delinsGA NP_277043.1:p.Glu176=
NM_000162.4:c.529_530delinsGA NP_000153.1:p.Glu177=
NM_001354800.1:c.529_530delinsGA NP_001341729.1:p.Glu177=
NM_033507.2:c.532_533delinsGA NP_277042.1:p.Glu178=
NM_033508.2:c.526_527delinsGA NP_277043.1:p.Glu176=
NM_000162.5:c.529_530delinsGA MANE Select NP_000153.1:p.Glu177=
NM_033507.3:c.532_533delinsGA NP_277042.1:p.Glu178=
NM_033508.3:c.526_527delinsGA NP_277043.1:p.Glu176=
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