Canonical Allele Identifier: CA2266876278

Gene: NOG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56594598C= , CM000679.2:g.56594598C=	GRCh38
NC_000017.10:g.54671959C= , CM000679.1:g.54671959C=	GRCh37
NC_000017.9:g.52026958C=	NCBI36
NG_011958.1:g.5900C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000332822.6:c.375C= MANE Select	ENSP00000328181.4:p.Phe125=
ENST00000332822.4:c.375C=	ENSP00000328181.4:p.Phe125=
NM_005450.4:c.375C=	NP_005441.1:p.Phe125=
NM_005450.6:c.375C= MANE Select	NP_005441.1:p.Phe125=