Canonical Allele Identifier: CA2842717614
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44150043dup , CM000669.2:g.44150043dup GRCh38
NC_000007.13:g.44189642dup , CM000669.1:g.44189642dup GRCh37
NC_000007.12:g.44156167dup NCBI36
NG_008847.1:g.44382dup
NG_008847.2:g.53129dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*504dup ENSP00000379142.4:n.*504dup
ENST00000616242.5:c.506dup ENSP00000482149.2:p.Phe171LeufsTer26
ENST00000682635.1:n.992dup
ENST00000345378.7:c.509dup ENSP00000223366.2:p.Phe172LeufsTer26
ENST00000403799.8:c.506dup MANE Select ENSP00000384247.3:p.Phe171LeufsTer26
ENST00000671824.1:c.506dup ENSP00000500264.1:p.Phe171LeufsTer26
ENST00000673284.1:c.506dup ENSP00000499852.1:p.Phe171LeufsTer26
ENST00000345378.6:c.509dup ENSP00000223366.2:p.Phe172LeufsTer26
ENST00000395796.7:c.503dup ENSP00000379142.3:p.Phe170LeufsTer26
ENST00000403799.7:c.506dup ENSP00000384247.3:p.Phe171LeufsTer26
ENST00000437084.1:c.455dup ENSP00000402840.1:p.Phe154LeufsTer26
ENST00000616242.4:c.503dup ENSP00000482149.1:p.Phe170LeufsTer26
NM_000162.3:c.506dup NP_000153.1:p.Phe171LeufsTer26
NM_033507.1:c.509dup NP_277042.1:p.Phe172LeufsTer26
NM_033508.1:c.503dup NP_277043.1:p.Phe170LeufsTer26
NM_000162.4:c.506dup NP_000153.1:p.Phe171LeufsTer26
NM_001354800.1:c.506dup NP_001341729.1:p.Phe171LeufsTer26
NM_033507.2:c.509dup NP_277042.1:p.Phe172LeufsTer26
NM_033508.2:c.503dup NP_277043.1:p.Phe170LeufsTer26
NM_000162.5:c.506dup MANE Select NP_000153.1:p.Phe171LeufsTer26
NM_033507.3:c.509dup NP_277042.1:p.Phe172LeufsTer26
NM_033508.3:c.503dup NP_277043.1:p.Phe170LeufsTer26
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