Canonical Allele Identifier: CA984892923
Gene: NOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595061_56595062insTTTTTTT , CM000679.2:g.56595061_56595062insTTTTTTT GRCh38
NC_000017.10:g.54672422_54672423insTTTTTTT , CM000679.1:g.54672422_54672423insTTTTTTT GRCh37
NC_000017.9:g.52027421_52027422insTTTTTTT NCBI36
NG_011958.1:g.6363_6364insTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*139_*140insTTTTTTT MANE Select ENSP00000328181.4:n.*139_*140insTTTTTTT
ENST00000332822.4:c.*139_*140insTTTTTTT ENSP00000328181.4:n.*139_*140insTTTTTTT
NM_005450.4:c.*139_*140insTTTTTTT NP_005441.1:n.*139_*140insTTTTTTT
NM_005450.6:c.*139_*140insTTTTTTT MANE Select NP_005441.1:n.*139_*140insTTTTTTT