Canonical Allele Identifier: CA1703636465
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44151011_44151012delinsTT , CM000669.2:g.44151011_44151012delinsTT GRCh38
NC_000007.13:g.44190610_44190611delinsTT , CM000669.1:g.44190610_44190611delinsTT GRCh37
NC_000007.12:g.44157135_44157136delinsTT NCBI36
NG_008847.1:g.43412_43413delinsAA
NG_008847.2:g.52159_52160delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*425_*426delinsAA ENSP00000379142.4:n.*425_*426delinsAA
ENST00000616242.5:c.427_428delinsAA ENSP00000482149.2:p.Lys143=
ENST00000682635.1:n.913_914delinsAA
ENST00000345378.7:c.430_431delinsAA ENSP00000223366.2:p.Lys144=
ENST00000403799.8:c.427_428delinsAA MANE Select ENSP00000384247.3:p.Lys143=
ENST00000671824.1:c.427_428delinsAA ENSP00000500264.1:p.Lys143=
ENST00000673284.1:c.427_428delinsAA ENSP00000499852.1:p.Lys143=
ENST00000345378.6:c.430_431delinsAA ENSP00000223366.2:p.Lys144=
ENST00000395796.7:c.424_425delinsAA ENSP00000379142.3:p.Lys142=
ENST00000403799.7:c.427_428delinsAA ENSP00000384247.3:p.Lys143=
ENST00000437084.1:c.376_377delinsAA ENSP00000402840.1:p.Lys126=
ENST00000616242.4:c.424_425delinsAA ENSP00000482149.1:p.Lys142=
NM_000162.3:c.427_428delinsAA NP_000153.1:p.Lys143=
NM_033507.1:c.430_431delinsAA NP_277042.1:p.Lys144=
NM_033508.1:c.424_425delinsAA NP_277043.1:p.Lys142=
NM_000162.4:c.427_428delinsAA NP_000153.1:p.Lys143=
NM_001354800.1:c.427_428delinsAA NP_001341729.1:p.Lys143=
NM_033507.2:c.430_431delinsAA NP_277042.1:p.Lys144=
NM_033508.2:c.424_425delinsAA NP_277043.1:p.Lys142=
NM_000162.5:c.427_428delinsAA MANE Select NP_000153.1:p.Lys143=
NM_033507.3:c.430_431delinsAA NP_277042.1:p.Lys144=
NM_033508.3:c.424_425delinsAA NP_277043.1:p.Lys142=
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