Canonical Allele Identifier: CA984892912
Gene: NOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595061_56595062del , CM000679.2:g.56595061_56595062del GRCh38
NC_000017.10:g.54672422_54672423del , CM000679.1:g.54672422_54672423del GRCh37
NC_000017.9:g.52027421_52027422del NCBI36
NG_011958.1:g.6363_6364del

Transcript Alleles

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