Canonical Allele Identifier: CA2695226696
Gene: NOG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594911_56594922del , CM000679.2:g.56594911_56594922del GRCh38
NC_000017.10:g.54672272_54672283del , CM000679.1:g.54672272_54672283del GRCh37
NC_000017.9:g.52027271_52027282del NCBI36
NG_011958.1:g.6213_6224del

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.688_699del MANE Select ENSP00000328181.4:p.Cys230_Ter233del
ENST00000332822.4:c.688_699del ENSP00000328181.4:p.Cys230_Ter233del
NM_005450.4:c.688_699del NP_005441.1:p.Cys230_Ter233del
NM_005450.6:c.688_699del MANE Select NP_005441.1:p.Cys230_Ter233del
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