Canonical Allele Identifier: CA2638880966
Gene: NOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594963_56594992dup , CM000679.2:g.56594963_56594992dup GRCh38
NC_000017.10:g.54672324_54672353dup , CM000679.1:g.54672324_54672353dup GRCh37
NC_000017.9:g.52027323_52027352dup NCBI36
NG_011958.1:g.6265_6294dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*41_*70dup MANE Select ENSP00000328181.4:n.*41_*70dup
ENST00000332822.4:c.*41_*70dup ENSP00000328181.4:n.*41_*70dup
NM_005450.4:c.*41_*70dup NP_005441.1:n.*41_*70dup
NM_005450.6:c.*41_*70dup MANE Select NP_005441.1:n.*41_*70dup