Canonical Allele Identifier: CA2266876459
Gene: NOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595005A= , CM000679.2:g.56595005A= GRCh38
NC_000017.10:g.54672366A= , CM000679.1:g.54672366A= GRCh37
NC_000017.9:g.52027365A= NCBI36
NG_011958.1:g.6307A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*83A= MANE Select ENSP00000328181.4:n.*83A=
ENST00000332822.4:c.*83A= ENSP00000328181.4:n.*83A=
NM_005450.4:c.*83A= NP_005441.1:n.*83A=
NM_005450.6:c.*83A= MANE Select NP_005441.1:n.*83A=