Canonical Allele Identifier: CA1703612710
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145269_44145279delinsCGCTCCTTGAA , CM000669.2:g.44145269_44145279delinsCGCTCCTTGAA GRCh38
NC_000007.13:g.44184868_44184878delinsCGCTCCTTGAA , CM000669.1:g.44184868_44184878delinsCGCTCCTTGAA GRCh37
NC_000007.12:g.44151393_44151403delinsCGCTCCTTGAA NCBI36
NG_008847.1:g.49145_49155delinsTTCAAGGAGCG
NG_008847.2:g.57892_57902delinsTTCAAGGAGCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1253_*1263delinsTTCAAGGAGCG ENSP00000379142.4:n.*1253_*1263delinsTTCAAGGAGCG
ENST00000616242.5:c.*375_*385delinsTTCAAGGAGCG ENSP00000482149.2:n.*375_*385delinsTTCAAGGAGCG
ENST00000683378.1:n.481_491delinsTTCAAGGAGCG
ENST00000336642.9:c.289_299delinsTTCAAGGAGCG ENSP00000338009.5:p.Phe97=
ENST00000345378.7:c.1258_1268delinsTTCAAGGAGCG ENSP00000223366.2:p.Phe420=
ENST00000403799.8:c.1255_1265delinsTTCAAGGAGCG MANE Select ENSP00000384247.3:p.Phe419=
ENST00000671824.1:c.1318_1328delinsTTCAAGGAGCG ENSP00000500264.1:p.Phe440=
ENST00000672743.1:n.267_277delinsTTCAAGGAGCG
ENST00000673284.1:c.1255_1265delinsTTCAAGGAGCG ENSP00000499852.1:p.Phe419=
ENST00000336642.8:c.307_317delinsTTCAAGGAGCG ENSP00000338009.4:p.Phe103=
ENST00000345378.6:c.1258_1268delinsTTCAAGGAGCG ENSP00000223366.2:p.Phe420=
ENST00000395796.7:c.1252_1262delinsTTCAAGGAGCG ENSP00000379142.3:p.Phe418=
ENST00000403799.7:c.1255_1265delinsTTCAAGGAGCG ENSP00000384247.3:p.Phe419=
ENST00000437084.1:c.1204_1214delinsTTCAAGGAGCG ENSP00000402840.1:p.Phe402=
ENST00000459642.1:n.635_645delinsTTCAAGGAGCG
ENST00000616242.4:c.1252_1262delinsTTCAAGGAGCG ENSP00000482149.1:p.Phe418=
NM_000162.3:c.1255_1265delinsTTCAAGGAGCG NP_000153.1:p.Phe419=
NM_033507.1:c.1258_1268delinsTTCAAGGAGCG NP_277042.1:p.Phe420=
NM_033508.1:c.1252_1262delinsTTCAAGGAGCG NP_277043.1:p.Phe418=
NM_000162.4:c.1255_1265delinsTTCAAGGAGCG NP_000153.1:p.Phe419=
NM_001354800.1:c.1255_1265delinsTTCAAGGAGCG NP_001341729.1:p.Phe419=
NM_001354801.1:c.244_254delinsTTCAAGGAGCG NP_001341730.1:p.Phe82=
NM_001354802.1:c.115_125delinsTTCAAGGAGCG NP_001341731.1:p.Phe39=
NM_001354803.1:c.289_299delinsTTCAAGGAGCG NP_001341732.1:p.Phe97=
NM_033507.2:c.1258_1268delinsTTCAAGGAGCG NP_277042.1:p.Phe420=
NM_033508.2:c.1252_1262delinsTTCAAGGAGCG NP_277043.1:p.Phe418=
XM_024446707.1:c.115_125delinsTTCAAGGAGCG XP_024302475.1:p.Phe39=
NM_000162.5:c.1255_1265delinsTTCAAGGAGCG MANE Select NP_000153.1:p.Phe419=
NM_033507.3:c.1258_1268delinsTTCAAGGAGCG NP_277042.1:p.Phe420=
NM_033508.3:c.1252_1262delinsTTCAAGGAGCG NP_277043.1:p.Phe418=
NM_001354803.2:c.289_299delinsTTCAAGGAGCG NP_001341732.1:p.Phe97=