Canonical Allele Identifier: CA1703636473
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44151045_44151046delinsCG , CM000669.2:g.44151045_44151046delinsCG GRCh38
NC_000007.13:g.44190644_44190645delinsCG , CM000669.1:g.44190644_44190645delinsCG GRCh37
NC_000007.12:g.44157169_44157170delinsCG NCBI36
NG_008847.1:g.43378_43379delinsCG
NG_008847.2:g.52125_52126delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*391_*392delinsCG ENSP00000379142.4:n.*391_*392delinsCG
ENST00000616242.5:c.393_394delinsCG ENSP00000482149.2:p.Ser131=
ENST00000682635.1:n.879_880delinsCG
ENST00000345378.7:c.396_397delinsCG ENSP00000223366.2:p.Ser132=
ENST00000403799.8:c.393_394delinsCG MANE Select ENSP00000384247.3:p.Ser131=
ENST00000671824.1:c.393_394delinsCG ENSP00000500264.1:p.Ser131=
ENST00000673284.1:c.393_394delinsCG ENSP00000499852.1:p.Ser131=
ENST00000345378.6:c.396_397delinsCG ENSP00000223366.2:p.Ser132=
ENST00000395796.7:c.390_391delinsCG ENSP00000379142.3:p.Ser130=
ENST00000403799.7:c.393_394delinsCG ENSP00000384247.3:p.Ser131=
ENST00000437084.1:c.364-22_364-21delinsCG ENSP00000402840.1:n.364-22_364-21delinsCG
ENST00000616242.4:c.390_391delinsCG ENSP00000482149.1:p.Ser130=
NM_000162.3:c.393_394delinsCG NP_000153.1:p.Ser131=
NM_033507.1:c.396_397delinsCG NP_277042.1:p.Ser132=
NM_033508.1:c.390_391delinsCG NP_277043.1:p.Ser130=
NM_000162.4:c.393_394delinsCG NP_000153.1:p.Ser131=
NM_001354800.1:c.393_394delinsCG NP_001341729.1:p.Ser131=
NM_033507.2:c.396_397delinsCG NP_277042.1:p.Ser132=
NM_033508.2:c.390_391delinsCG NP_277043.1:p.Ser130=
NM_000162.5:c.393_394delinsCG MANE Select NP_000153.1:p.Ser131=
NM_033507.3:c.396_397delinsCG NP_277042.1:p.Ser132=
NM_033508.3:c.390_391delinsCG NP_277043.1:p.Ser130=
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