Canonical Allele Identifier: CA2266876298
Gene: NOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594645T= , CM000679.2:g.56594645T= GRCh38
NC_000017.10:g.54672006T= , CM000679.1:g.54672006T= GRCh37
NC_000017.9:g.52027005T= NCBI36
NG_011958.1:g.5947T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.422T= MANE Select ENSP00000328181.4:p.Leu141=
ENST00000332822.4:c.422T= ENSP00000328181.4:p.Leu141=
NM_005450.4:c.422T= NP_005441.1:p.Leu141=
NM_005450.6:c.422T= MANE Select NP_005441.1:p.Leu141=