Canonical Allele Identifier: CA2775231443
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44151168_44151171del , CM000669.2:g.44151168_44151171del GRCh38
NC_000007.13:g.44190767_44190770del , CM000669.1:g.44190767_44190770del GRCh37
NC_000007.12:g.44157292_44157295del NCBI36
NG_008847.1:g.43253_43256del
NG_008847.2:g.52000_52003del

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*362-96_*362-93del ENSP00000379142.4:n.*362-96_*362-93del
ENST00000616242.5:c.364-96_364-93del ENSP00000482149.2:n.364-96_364-93del
ENST00000682635.1:n.850-96_850-93del
ENST00000345378.7:c.367-96_367-93del ENSP00000223366.2:n.367-96_367-93del
ENST00000403799.8:c.364-96_364-93del MANE Select ENSP00000384247.3:n.364-96_364-93del
ENST00000671824.1:c.364-96_364-93del ENSP00000500264.1:n.364-96_364-93del
ENST00000673284.1:c.364-96_364-93del ENSP00000499852.1:n.364-96_364-93del
ENST00000345378.6:c.367-96_367-93del ENSP00000223366.2:n.367-96_367-93del
ENST00000395796.7:c.361-96_361-93del ENSP00000379142.3:n.361-96_361-93del
ENST00000403799.7:c.364-96_364-93del ENSP00000384247.3:n.364-96_364-93del
ENST00000437084.1:c.364-147_364-144del ENSP00000402840.1:n.364-147_364-144del
ENST00000616242.4:c.361-96_361-93del ENSP00000482149.1:n.361-96_361-93del
NM_000162.3:c.364-96_364-93del NP_000153.1:n.364-96_364-93del
NM_033507.1:c.367-96_367-93del NP_277042.1:n.367-96_367-93del
NM_033508.1:c.361-96_361-93del NP_277043.1:n.361-96_361-93del
NM_000162.4:c.364-96_364-93del NP_000153.1:n.364-96_364-93del
NM_001354800.1:c.364-96_364-93del NP_001341729.1:n.364-96_364-93del
NM_033507.2:c.367-96_367-93del NP_277042.1:n.367-96_367-93del
NM_033508.2:c.361-96_361-93del NP_277043.1:n.361-96_361-93del
NM_000162.5:c.364-96_364-93del MANE Select NP_000153.1:n.364-96_364-93del
NM_033507.3:c.367-96_367-93del NP_277042.1:n.367-96_367-93del
NM_033508.3:c.361-96_361-93del NP_277043.1:n.361-96_361-93del
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