Canonical Allele Identifier: CA2775230998
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147482del , CM000669.2:g.44147482del GRCh38
NC_000007.13:g.44187081del , CM000669.1:g.44187081del GRCh37
NC_000007.12:g.44153606del NCBI36
NG_008847.1:g.46945del
NG_008847.2:g.55692del

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*861+171del ENSP00000379142.4:n.*861+171del
ENST00000616242.5:c.853+181del ENSP00000482149.2:n.853+181del
ENST00000345378.7:c.866+171del ENSP00000223366.2:n.866+171del
ENST00000403799.8:c.863+171del MANE Select ENSP00000384247.3:n.863+171del
ENST00000671824.1:c.854-66del ENSP00000500264.1:n.854-66del
ENST00000673284.1:c.863+171del ENSP00000499852.1:n.863+171del
ENST00000345378.6:c.866+171del ENSP00000223366.2:n.866+171del
ENST00000395796.7:c.860+171del ENSP00000379142.3:n.860+171del
ENST00000403799.7:c.863+171del ENSP00000384247.3:n.863+171del
ENST00000437084.1:c.812+171del ENSP00000402840.1:n.812+171del
ENST00000616242.4:c.860+171del ENSP00000482149.1:n.860+171del
NM_000162.3:c.863+171del NP_000153.1:n.863+171del
NM_033507.1:c.866+171del NP_277042.1:n.866+171del
NM_033508.1:c.860+171del NP_277043.1:n.860+171del
NM_000162.4:c.863+171del NP_000153.1:n.863+171del
NM_001354800.1:c.863+171del NP_001341729.1:n.863+171del
NM_033507.2:c.866+171del NP_277042.1:n.866+171del
NM_033508.2:c.860+171del NP_277043.1:n.860+171del
NM_000162.5:c.863+171del MANE Select NP_000153.1:n.863+171del
NM_033507.3:c.866+171del NP_277042.1:n.866+171del
NM_033508.3:c.860+171del NP_277043.1:n.860+171del
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