Canonical Allele Identifier: CA2266876439
Gene: NOG HGNC NCBI

Linked Data

dbSNP Id: rs2052473477

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594979del , CM000679.2:g.56594979del GRCh38
NC_000017.10:g.54672340del , CM000679.1:g.54672340del GRCh37
NC_000017.9:g.52027339del NCBI36
NG_011958.1:g.6281del

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*57del MANE Select ENSP00000328181.4:n.*57del
ENST00000332822.4:c.*57del ENSP00000328181.4:n.*57del
NM_005450.4:c.*57del NP_005441.1:n.*57del
NM_005450.6:c.*57del MANE Select NP_005441.1:n.*57del