Canonical Allele Identifier: CA1703612513
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44144913_44144919delinsTTCCTGC , CM000669.2:g.44144913_44144919delinsTTCCTGC GRCh38
NC_000007.13:g.44184512_44184518delinsTTCCTGC , CM000669.1:g.44184512_44184518delinsTTCCTGC GRCh37
NC_000007.12:g.44151037_44151043delinsTTCCTGC NCBI36
NG_008847.1:g.49505_49511delinsGCAGGAA
NG_008847.2:g.58252_58258delinsGCAGGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1613_*1619delinsGCAGGAA ENSP00000379142.4:n.*1613_*1619delinsGCAGGAA
ENST00000616242.5:c.*735_*741delinsGCAGGAA ENSP00000482149.2:n.*735_*741delinsGCAGGAA
ENST00000683378.1:n.841_847delinsGCAGGAA
ENST00000336642.9:c.*217_*223delinsGCAGGAA ENSP00000338009.5:n.*217_*223delinsGCAGGAA
ENST00000345378.7:c.*217_*223delinsGCAGGAA ENSP00000223366.2:n.*217_*223delinsGCAGGAA
ENST00000403799.8:c.*217_*223delinsGCAGGAA MANE Select ENSP00000384247.3:n.*217_*223delinsGCAGGAA
ENST00000671824.1:c.*217_*223delinsGCAGGAA ENSP00000500264.1:n.*217_*223delinsGCAGGAA
ENST00000672743.1:n.381+246_381+252delinsGCAGGAA
ENST00000673284.1:c.1369+246_1369+252delinsGCAGGAA ENSP00000499852.1:n.1369+246_1369+252delinsGCAGGAA
ENST00000336642.8:c.667_673delinsGCAGGAA ENSP00000338009.4:n.667_673delinsGCAGGAA
ENST00000345378.6:c.*217_*223delinsGCAGGAA ENSP00000223366.2:n.*217_*223delinsGCAGGAA
ENST00000395796.7:c.*217_*223delinsGCAGGAA ENSP00000379142.3:n.*217_*223delinsGCAGGAA
ENST00000403799.7:c.*217_*223delinsGCAGGAA ENSP00000384247.3:n.*217_*223delinsGCAGGAA
ENST00000459642.1:n.995_1001delinsGCAGGAA
ENST00000616242.4:c.1612_1618delinsGCAGGAA ENSP00000482149.1:n.1612_1618delinsGCAGGAA
NM_000162.3:c.*217_*223delinsGCAGGAA NP_000153.1:n.*217_*223delinsGCAGGAA
NM_033507.1:c.*217_*223delinsGCAGGAA NP_277042.1:n.*217_*223delinsGCAGGAA
NM_033508.1:c.*217_*223delinsGCAGGAA NP_277043.1:n.*217_*223delinsGCAGGAA
NM_000162.4:c.*217_*223delinsGCAGGAA NP_000153.1:n.*217_*223delinsGCAGGAA
NM_001354800.1:c.1369+246_1369+252delinsGCAGGAA NP_001341729.1:n.1369+246_1369+252delinsGCAGGAA
NM_001354801.1:c.*217_*223delinsGCAGGAA NP_001341730.1:n.*217_*223delinsGCAGGAA
NM_001354802.1:c.229+246_229+252delinsGCAGGAA NP_001341731.1:n.229+246_229+252delinsGCAGGAA
NM_001354803.1:c.*217_*223delinsGCAGGAA NP_001341732.1:n.*217_*223delinsGCAGGAA
NM_033507.2:c.*217_*223delinsGCAGGAA NP_277042.1:n.*217_*223delinsGCAGGAA
NM_033508.2:c.*217_*223delinsGCAGGAA NP_277043.1:n.*217_*223delinsGCAGGAA
XM_024446707.1:c.*217_*223delinsGCAGGAA XP_024302475.1:n.*217_*223delinsGCAGGAA
NM_000162.5:c.*217_*223delinsGCAGGAA MANE Select NP_000153.1:n.*217_*223delinsGCAGGAA
NM_033507.3:c.*217_*223delinsGCAGGAA NP_277042.1:n.*217_*223delinsGCAGGAA
NM_033508.3:c.*217_*223delinsGCAGGAA NP_277043.1:n.*217_*223delinsGCAGGAA
NM_001354803.2:c.*217_*223delinsGCAGGAA NP_001341732.1:n.*217_*223delinsGCAGGAA