Canonical Allele Identifier: CA2638881009
Gene: NOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595010_56595011insGC , CM000679.2:g.56595010_56595011insGC GRCh38
NC_000017.10:g.54672371_54672372insGC , CM000679.1:g.54672371_54672372insGC GRCh37
NC_000017.9:g.52027370_52027371insGC NCBI36
NG_011958.1:g.6312_6313insGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*88_*89insGC MANE Select ENSP00000328181.4:n.*88_*89insGC
ENST00000332822.4:c.*88_*89insGC ENSP00000328181.4:n.*88_*89insGC
NM_005450.4:c.*88_*89insGC NP_005441.1:n.*88_*89insGC
NM_005450.6:c.*88_*89insGC MANE Select NP_005441.1:n.*88_*89insGC