Canonical Allele Identifier: CA2266876413
Gene: NOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594945A= , CM000679.2:g.56594945A= GRCh38
NC_000017.10:g.54672306A= , CM000679.1:g.54672306A= GRCh37
NC_000017.9:g.52027305A= NCBI36
NG_011958.1:g.6247A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*23A= MANE Select ENSP00000328181.4:n.*23A=
ENST00000332822.4:c.*23A= ENSP00000328181.4:n.*23A=
NM_005450.4:c.*23A= NP_005441.1:n.*23A=
NM_005450.6:c.*23A= MANE Select NP_005441.1:n.*23A=