Canonical Allele Identifier: CA2266876456
Gene: NOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595002A= , CM000679.2:g.56595002A= GRCh38
NC_000017.10:g.54672363A= , CM000679.1:g.54672363A= GRCh37
NC_000017.9:g.52027362A= NCBI36
NG_011958.1:g.6304A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*80A= MANE Select ENSP00000328181.4:n.*80A=
ENST00000332822.4:c.*80A= ENSP00000328181.4:n.*80A=
NM_005450.4:c.*80A= NP_005441.1:n.*80A=
NM_005450.6:c.*80A= MANE Select NP_005441.1:n.*80A=