Canonical Allele Identifier: CA399966022
Gene: NOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594620A>C , CM000679.2:g.56594620A>C GRCh38
NC_000017.10:g.54671981A>C , CM000679.1:g.54671981A>C GRCh37
NC_000017.9:g.52026980A>C NCBI36
NG_011958.1:g.5922A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.397A>C MANE Select ENSP00000328181.4:p.Lys133Gln
ENST00000332822.4:c.397A>C ENSP00000328181.4:p.Lys133Gln
NM_005450.4:c.397A>C NP_005441.1:p.Lys133Gln
NM_005450.6:c.397A>C MANE Select NP_005441.1:p.Lys133Gln