Canonical Allele Identifier: CA1703634870
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147658_44147659delinsAC , CM000669.2:g.44147658_44147659delinsAC GRCh38
NC_000007.13:g.44187257_44187258delinsAC , CM000669.1:g.44187257_44187258delinsAC GRCh37
NC_000007.12:g.44153782_44153783delinsAC NCBI36
NG_008847.1:g.46765_46766delinsGT
NG_008847.2:g.55512_55513delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*852_*853delinsGT ENSP00000379142.4:n.*852_*853delinsGT
ENST00000616242.5:c.853+1_853+2delinsGT ENSP00000482149.2:n.853+1_853+2delinsGT
ENST00000345378.7:c.857_858delinsGT ENSP00000223366.2:p.Gly286=
ENST00000403799.8:c.854_855delinsGT MANE Select ENSP00000384247.3:p.Gly285=
ENST00000671824.1:c.853+1_853+2delinsGT ENSP00000500264.1:n.853+1_853+2delinsGT
ENST00000673284.1:c.854_855delinsGT ENSP00000499852.1:p.Gly285=
ENST00000345378.6:c.857_858delinsGT ENSP00000223366.2:p.Gly286=
ENST00000395796.7:c.851_852delinsGT ENSP00000379142.3:p.Gly284=
ENST00000403799.7:c.854_855delinsGT ENSP00000384247.3:p.Gly285=
ENST00000437084.1:c.803_804delinsGT ENSP00000402840.1:p.Gly268=
ENST00000616242.4:c.851_852delinsGT ENSP00000482149.1:p.Gly284=
NM_000162.3:c.854_855delinsGT NP_000153.1:p.Gly285=
NM_033507.1:c.857_858delinsGT NP_277042.1:p.Gly286=
NM_033508.1:c.851_852delinsGT NP_277043.1:p.Gly284=
NM_000162.4:c.854_855delinsGT NP_000153.1:p.Gly285=
NM_001354800.1:c.854_855delinsGT NP_001341729.1:p.Gly285=
NM_033507.2:c.857_858delinsGT NP_277042.1:p.Gly286=
NM_033508.2:c.851_852delinsGT NP_277043.1:p.Gly284=
NM_000162.5:c.854_855delinsGT MANE Select NP_000153.1:p.Gly285=
NM_033507.3:c.857_858delinsGT NP_277042.1:p.Gly286=
NM_033508.3:c.851_852delinsGT NP_277043.1:p.Gly284=
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