Canonical Allele Identifier: CA2266876501
Gene: NOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595055T= , CM000679.2:g.56595055T= GRCh38
NC_000017.10:g.54672416T= , CM000679.1:g.54672416T= GRCh37
NC_000017.9:g.52027415T= NCBI36
NG_011958.1:g.6357T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*133T= MANE Select ENSP00000328181.4:n.*133T=
ENST00000332822.4:c.*133T= ENSP00000328181.4:n.*133T=
NM_005450.4:c.*133T= NP_005441.1:n.*133T=
NM_005450.6:c.*133T= MANE Select NP_005441.1:n.*133T=