Canonical Allele Identifier: CA2266876453
Gene: NOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595000C= , CM000679.2:g.56595000C= GRCh38
NC_000017.10:g.54672361C= , CM000679.1:g.54672361C= GRCh37
NC_000017.9:g.52027360C= NCBI36
NG_011958.1:g.6302C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*78C= MANE Select ENSP00000328181.4:n.*78C=
ENST00000332822.4:c.*78C= ENSP00000328181.4:n.*78C=
NM_005450.4:c.*78C= NP_005441.1:n.*78C=
NM_005450.6:c.*78C= MANE Select NP_005441.1:n.*78C=