Canonical Allele Identifier: CA2695203017
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44153326_44153328delinsTTG , CM000669.2:g.44153326_44153328delinsTTG GRCh38
NC_000007.13:g.44192925_44192927delinsTTG , CM000669.1:g.44192925_44192927delinsTTG GRCh37
NC_000007.12:g.44159450_44159452delinsTTG NCBI36
NG_008847.1:g.41096_41098delinsCAA
NG_008847.2:g.49843_49845delinsCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*179_*181delinsCAA ENSP00000379142.4:n.*179_*181delinsCAA
ENST00000616242.5:c.181_183delinsCAA ENSP00000482149.2:p.Tyr61Gln
ENST00000682635.1:n.667_669delinsCAA
ENST00000345378.7:c.184_186delinsCAA ENSP00000223366.2:p.Tyr62Gln
ENST00000403799.8:c.181_183delinsCAA MANE Select ENSP00000384247.3:p.Tyr61Gln
ENST00000671824.1:c.181_183delinsCAA ENSP00000500264.1:p.Tyr61Gln
ENST00000673284.1:c.181_183delinsCAA ENSP00000499852.1:p.Tyr61Gln
ENST00000345378.6:c.184_186delinsCAA ENSP00000223366.2:p.Tyr62Gln
ENST00000395796.7:c.178_180delinsCAA ENSP00000379142.3:p.Tyr60Gln
ENST00000403799.7:c.181_183delinsCAA ENSP00000384247.3:p.Tyr61Gln
ENST00000437084.1:c.181_183delinsCAA ENSP00000402840.1:p.Tyr61Gln
ENST00000616242.4:c.178_180delinsCAA ENSP00000482149.1:p.Tyr60Gln
NM_000162.3:c.181_183delinsCAA NP_000153.1:p.Tyr61Gln
NM_033507.1:c.184_186delinsCAA NP_277042.1:p.Tyr62Gln
NM_033508.1:c.178_180delinsCAA NP_277043.1:p.Tyr60Gln
NM_000162.4:c.181_183delinsCAA NP_000153.1:p.Tyr61Gln
NM_001354800.1:c.181_183delinsCAA NP_001341729.1:p.Tyr61Gln
NM_033507.2:c.184_186delinsCAA NP_277042.1:p.Tyr62Gln
NM_033508.2:c.178_180delinsCAA NP_277043.1:p.Tyr60Gln
NM_000162.5:c.181_183delinsCAA MANE Select NP_000153.1:p.Tyr61Gln
NM_033507.3:c.184_186delinsCAA NP_277042.1:p.Tyr62Gln
NM_033508.3:c.178_180delinsCAA NP_277043.1:p.Tyr60Gln
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