Canonical Allele Identifier: CA2266876300
Gene: NOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594648G= , CM000679.2:g.56594648G= GRCh38
NC_000017.10:g.54672009G= , CM000679.1:g.54672009G= GRCh37
NC_000017.9:g.52027008G= NCBI36
NG_011958.1:g.5950G=

Transcript Alleles

HGVS Amino-acid change
ENST00000332822.6:c.425G= MANE Select ENSP00000328181.4:p.Arg142=
ENST00000332822.4:c.425G= ENSP00000328181.4:p.Arg142=
NM_005450.4:c.425G= NP_005441.1:p.Arg142=
NM_005450.6:c.425G= MANE Select NP_005441.1:p.Arg142=