Canonical Allele Identifier: CA2775231421
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44151120_44151140del , CM000669.2:g.44151120_44151140del GRCh38
NC_000007.13:g.44190719_44190739del , CM000669.1:g.44190719_44190739del GRCh37
NC_000007.12:g.44157244_44157264del NCBI36
NG_008847.1:g.43284_43304del
NG_008847.2:g.52031_52051del

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*362-65_*362-45del ENSP00000379142.4:n.*362-65_*362-45del
ENST00000616242.5:c.364-65_364-45del ENSP00000482149.2:n.364-65_364-45del
ENST00000682635.1:n.850-65_850-45del
ENST00000345378.7:c.367-65_367-45del ENSP00000223366.2:n.367-65_367-45del
ENST00000403799.8:c.364-65_364-45del MANE Select ENSP00000384247.3:n.364-65_364-45del
ENST00000671824.1:c.364-65_364-45del ENSP00000500264.1:n.364-65_364-45del
ENST00000673284.1:c.364-65_364-45del ENSP00000499852.1:n.364-65_364-45del
ENST00000345378.6:c.367-65_367-45del ENSP00000223366.2:n.367-65_367-45del
ENST00000395796.7:c.361-65_361-45del ENSP00000379142.3:n.361-65_361-45del
ENST00000403799.7:c.364-65_364-45del ENSP00000384247.3:n.364-65_364-45del
ENST00000437084.1:c.364-116_364-96del ENSP00000402840.1:n.364-116_364-96del
ENST00000616242.4:c.361-65_361-45del ENSP00000482149.1:n.361-65_361-45del
NM_000162.3:c.364-65_364-45del NP_000153.1:n.364-65_364-45del
NM_033507.1:c.367-65_367-45del NP_277042.1:n.367-65_367-45del
NM_033508.1:c.361-65_361-45del NP_277043.1:n.361-65_361-45del
NM_000162.4:c.364-65_364-45del NP_000153.1:n.364-65_364-45del
NM_001354800.1:c.364-65_364-45del NP_001341729.1:n.364-65_364-45del
NM_033507.2:c.367-65_367-45del NP_277042.1:n.367-65_367-45del
NM_033508.2:c.361-65_361-45del NP_277043.1:n.361-65_361-45del
NM_000162.5:c.364-65_364-45del MANE Select NP_000153.1:n.364-65_364-45del
NM_033507.3:c.367-65_367-45del NP_277042.1:n.367-65_367-45del
NM_033508.3:c.361-65_361-45del NP_277043.1:n.361-65_361-45del
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