Canonical Allele Identifier: CA2695226621
Gene: NOG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594483_56594524del , CM000679.2:g.56594483_56594524del GRCh38
NC_000017.10:g.54671844_54671885del , CM000679.1:g.54671844_54671885del GRCh37
NC_000017.9:g.52026843_52026884del NCBI36
NG_011958.1:g.5785_5826del

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.260_301del MANE Select ENSP00000328181.4:p.Arg87_Asp100del
ENST00000332822.4:c.260_301del ENSP00000328181.4:p.Arg87_Asp100del
NM_005450.4:c.260_301del NP_005441.1:p.Arg87_Asp100del
NM_005450.6:c.260_301del MANE Select NP_005441.1:p.Arg87_Asp100del
Search 100 bp 5'
Search 100 bp 3'