Canonical Allele Identifier: CA2842021911
Gene: NOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594556dup , CM000679.2:g.56594556dup GRCh38
NC_000017.10:g.54671917dup , CM000679.1:g.54671917dup GRCh37
NC_000017.9:g.52026916dup NCBI36
NG_011958.1:g.5858dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.333dup MANE Select ENSP00000328181.4:p.Pro112AlafsTer?
ENST00000332822.4:c.333dup ENSP00000328181.4:p.Pro112AlafsTer?
NM_005450.4:c.333dup NP_005441.1:p.Pro112AlafsTer?
NM_005450.6:c.333dup MANE Select NP_005441.1:p.Pro112AlafsTer?