Canonical Allele Identifier: CA2266876526
Gene: NOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595089T= , CM000679.2:g.56595089T= GRCh38
NC_000017.10:g.54672450T= , CM000679.1:g.54672450T= GRCh37
NC_000017.9:g.52027449T= NCBI36
NG_011958.1:g.6391T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*167T= MANE Select ENSP00000328181.4:n.*167T=
ENST00000332822.4:c.*167T= ENSP00000328181.4:n.*167T=
NM_005450.4:c.*167T= NP_005441.1:n.*167T=
NM_005450.6:c.*167T= MANE Select NP_005441.1:n.*167T=