Canonical Allele Identifier: CA2576328698
Gene: NOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594932dup , CM000679.2:g.56594932dup GRCh38
NC_000017.10:g.54672293dup , CM000679.1:g.54672293dup GRCh37
NC_000017.9:g.52027292dup NCBI36
NG_011958.1:g.6234dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*10dup MANE Select ENSP00000328181.4:n.*10dup
ENST00000332822.4:c.*10dup ENSP00000328181.4:n.*10dup
NM_005450.4:c.*10dup NP_005441.1:n.*10dup
NM_005450.6:c.*10dup MANE Select NP_005441.1:n.*10dup