Canonical Allele Identifier: CA1328827426
Gene: CNOT9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218584693T= , CM000664.2:g.218584693T= GRCh38
NC_000002.11:g.219449416T= , CM000664.1:g.219449416T= GRCh37
NC_000002.10:g.219157660T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000273064.11:c.402T= MANE Select ENSP00000273064.6:p.Tyr134=
ENST00000273064.10:c.402T= ENSP00000273064.6:p.Tyr134=
ENST00000295701.9:c.402T= ENSP00000295701.5:p.Tyr134=
ENST00000542068.5:c.402T= ENSP00000443687.1:p.Tyr134=
ENST00000627282.2:c.402T= ENSP00000486540.1:p.Tyr134=
NM_001271634.1:c.402T= NP_001258563.1:p.Tyr134=
NM_001271635.1:c.402T= NP_001258564.1:p.Tyr134=
NM_005444.2:c.402T= NP_005435.1:p.Tyr134=
NR_073390.1:n.695+1607T=
XM_011512138.1:c.243T= XP_011510440.1:p.Tyr81=
XM_011512138.3:c.243T= XP_011510440.1:p.Tyr81=
XM_017005248.1:c.240T= XP_016860737.1:p.Tyr80=
XM_017005249.2:c.243T= XP_016860738.1:p.Tyr81=
NM_001271634.2:c.402T= NP_001258563.1:p.Tyr134=
NM_005444.3:c.402T= MANE Select NP_005435.1:p.Tyr134=
NR_073390.2:n.436+1607T=
NM_001271635.2:c.402T= NP_001258564.1:p.Tyr134=