Canonical Allele Identifier: CA350568212
Gene: CNOT9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218583040A>T , CM000664.2:g.218583040A>T GRCh38
NC_000002.11:g.219447763A>T , CM000664.1:g.219447763A>T GRCh37
NC_000002.10:g.219156007A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000273064.11:c.274A>T MANE Select ENSP00000273064.6:p.Asn92Tyr
ENST00000273064.10:c.274A>T ENSP00000273064.6:p.Asn92Tyr
ENST00000295701.9:c.274A>T ENSP00000295701.5:p.Asn92Tyr
ENST00000432877.5:c.*166A>T ENSP00000392394.1:n.*166A>T
ENST00000542068.5:c.274A>T ENSP00000443687.1:p.Asn92Tyr
ENST00000627282.2:c.274A>T ENSP00000486540.1:p.Asn92Tyr
NM_001271634.1:c.274A>T NP_001258563.1:p.Asn92Tyr
NM_001271635.1:c.274A>T NP_001258564.1:p.Asn92Tyr
NM_005444.2:c.274A>T NP_005435.1:p.Asn92Tyr
NR_073390.1:n.649A>T
XM_011512138.1:c.115A>T XP_011510440.1:p.Asn39Tyr
XM_011512138.3:c.115A>T XP_011510440.1:p.Asn39Tyr
XM_017005248.1:c.112A>T XP_016860737.1:p.Asn38Tyr
XM_017005249.2:c.115A>T XP_016860738.1:p.Asn39Tyr
NM_001271634.2:c.274A>T NP_001258563.1:p.Asn92Tyr
NM_005444.3:c.274A>T MANE Select NP_005435.1:p.Asn92Tyr
NR_073390.2:n.390A>T
NM_001271635.2:c.274A>T NP_001258564.1:p.Asn92Tyr