Canonical Allele Identifier: CA656509821
Gene: NOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595059dup , CM000679.2:g.56595059dup GRCh38
NC_000017.10:g.54672420dup , CM000679.1:g.54672420dup GRCh37
NC_000017.9:g.52027419dup NCBI36
NG_011958.1:g.6361dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*137dup MANE Select ENSP00000328181.4:n.*137dup
ENST00000332822.4:c.*137dup ENSP00000328181.4:n.*137dup
NM_005450.4:c.*137dup NP_005441.1:n.*137dup
NM_005450.6:c.*137dup MANE Select NP_005441.1:n.*137dup