Canonical Allele Identifier: CA2266876441
Gene: NOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594979C= , CM000679.2:g.56594979C= GRCh38
NC_000017.10:g.54672340C= , CM000679.1:g.54672340C= GRCh37
NC_000017.9:g.52027339C= NCBI36
NG_011958.1:g.6281C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*57C= MANE Select ENSP00000328181.4:n.*57C=
ENST00000332822.4:c.*57C= ENSP00000328181.4:n.*57C=
NM_005450.4:c.*57C= NP_005441.1:n.*57C=
NM_005450.6:c.*57C= MANE Select NP_005441.1:n.*57C=