Canonical Allele Identifier: CA2695203103
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147747_44147750dup , CM000669.2:g.44147747_44147750dup GRCh38
NC_000007.13:g.44187346_44187349dup , CM000669.1:g.44187346_44187349dup GRCh37
NC_000007.12:g.44153871_44153874dup NCBI36
NG_008847.1:g.46675_46678dup
NG_008847.2:g.55422_55425dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*762_*765dup ENSP00000379142.4:n.*762_*765dup
ENST00000616242.5:c.764_767dup ENSP00000482149.2:p.Glu256AspfsTer20
ENST00000345378.7:c.767_770dup ENSP00000223366.2:p.Glu257AspfsTer20
ENST00000403799.8:c.764_767dup MANE Select ENSP00000384247.3:p.Glu256AspfsTer20
ENST00000671824.1:c.764_767dup ENSP00000500264.1:p.Glu256AspfsTer20
ENST00000673284.1:c.764_767dup ENSP00000499852.1:p.Glu256AspfsTer20
ENST00000345378.6:c.767_770dup ENSP00000223366.2:p.Glu257AspfsTer20
ENST00000395796.7:c.761_764dup ENSP00000379142.3:p.Glu255AspfsTer20
ENST00000403799.7:c.764_767dup ENSP00000384247.3:p.Glu256AspfsTer20
ENST00000437084.1:c.713_716dup ENSP00000402840.1:p.Glu239AspfsTer20
ENST00000616242.4:c.761_764dup ENSP00000482149.1:p.Glu255AspfsTer20
NM_000162.3:c.764_767dup NP_000153.1:p.Glu256AspfsTer20
NM_033507.1:c.767_770dup NP_277042.1:p.Glu257AspfsTer20
NM_033508.1:c.761_764dup NP_277043.1:p.Glu255AspfsTer20
XR_927223.1:n.81_82+2dup
NM_000162.4:c.764_767dup NP_000153.1:p.Glu256AspfsTer20
NM_001354800.1:c.764_767dup NP_001341729.1:p.Glu256AspfsTer20
NM_033507.2:c.767_770dup NP_277042.1:p.Glu257AspfsTer20
NM_033508.2:c.761_764dup NP_277043.1:p.Glu255AspfsTer20
XR_927223.2:n.81_82+2dup
NM_000162.5:c.764_767dup MANE Select NP_000153.1:p.Glu256AspfsTer20
NM_033507.3:c.767_770dup NP_277042.1:p.Glu257AspfsTer20
NM_033508.3:c.761_764dup NP_277043.1:p.Glu255AspfsTer20