Canonical Allele Identifier: CA2266876299
Gene: NOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594646G= , CM000679.2:g.56594646G= GRCh38
NC_000017.10:g.54672007G= , CM000679.1:g.54672007G= GRCh37
NC_000017.9:g.52027006G= NCBI36
NG_011958.1:g.5948G=

Transcript Alleles

HGVS Amino-acid change
ENST00000332822.6:c.423G= MANE Select ENSP00000328181.4:p.Leu141=
ENST00000332822.4:c.423G= ENSP00000328181.4:p.Leu141=
NM_005450.4:c.423G= NP_005441.1:p.Leu141=
NM_005450.6:c.423G= MANE Select NP_005441.1:p.Leu141=