Canonical Allele Identifier: CA984892908
Gene: NOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595059_56595060insTTTTTG , CM000679.2:g.56595059_56595060insTTTTTG GRCh38
NC_000017.10:g.54672420_54672421insTTTTTG , CM000679.1:g.54672420_54672421insTTTTTG GRCh37
NC_000017.9:g.52027419_52027420insTTTTTG NCBI36
NG_011958.1:g.6361_6362insTTTTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*137_*138insTTTTTG MANE Select ENSP00000328181.4:n.*137_*138insTTTTTG
ENST00000332822.4:c.*137_*138insTTTTTG ENSP00000328181.4:n.*137_*138insTTTTTG
NM_005450.4:c.*137_*138insTTTTTG NP_005441.1:n.*137_*138insTTTTTG
NM_005450.6:c.*137_*138insTTTTTG MANE Select NP_005441.1:n.*137_*138insTTTTTG