Canonical Allele Identifier: CA2266876303
Gene: NOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594658A= , CM000679.2:g.56594658A= GRCh38
NC_000017.10:g.54672019A= , CM000679.1:g.54672019A= GRCh37
NC_000017.9:g.52027018A= NCBI36
NG_011958.1:g.5960A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.435A= MANE Select ENSP00000328181.4:p.Leu145=
ENST00000332822.4:c.435A= ENSP00000328181.4:p.Leu145=
NM_005450.4:c.435A= NP_005441.1:p.Leu145=
NM_005450.6:c.435A= MANE Select NP_005441.1:p.Leu145=