Canonical Allele Identifier: CA2266876354
Gene: NOG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594810A= , CM000679.2:g.56594810A= GRCh38
NC_000017.10:g.54672171A= , CM000679.1:g.54672171A= GRCh37
NC_000017.9:g.52027170A= NCBI36
NG_011958.1:g.6112A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.587A= MANE Select ENSP00000328181.4:p.Lys196=
ENST00000332822.4:c.587A= ENSP00000328181.4:p.Lys196=
NM_005450.4:c.587A= NP_005441.1:p.Lys196=
NM_005450.6:c.587A= MANE Select NP_005441.1:p.Lys196=
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