Canonical Allele Identifier: CA2545567361
Gene: NOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595066C>T , CM000679.2:g.56595066C>T GRCh38
NC_000017.10:g.54672427C>T , CM000679.1:g.54672427C>T GRCh37
NC_000017.9:g.52027426C>T NCBI36
NG_011958.1:g.6368C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*144C>T MANE Select ENSP00000328181.4:n.*144C>T
ENST00000332822.4:c.*144C>T ENSP00000328181.4:n.*144C>T
NM_005450.4:c.*144C>T NP_005441.1:n.*144C>T
NM_005450.6:c.*144C>T MANE Select NP_005441.1:n.*144C>T