Canonical Allele Identifier: CA1328827404
Gene: CNOT9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218584598T= , CM000664.2:g.218584598T= GRCh38
NC_000002.11:g.219449321T= , CM000664.1:g.219449321T= GRCh37
NC_000002.10:g.219157565T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000273064.11:c.321-14T= MANE Select ENSP00000273064.6:n.321-14T=
ENST00000273064.10:c.321-14T= ENSP00000273064.6:n.321-14T=
ENST00000295701.9:c.321-14T= ENSP00000295701.5:n.321-14T=
ENST00000432877.5:c.*213-14T= ENSP00000392394.1:n.*213-14T=
ENST00000542068.5:c.321-14T= ENSP00000443687.1:n.321-14T=
ENST00000627282.2:c.321-14T= ENSP00000486540.1:n.321-14T=
NM_001271634.1:c.321-14T= NP_001258563.1:n.321-14T=
NM_001271635.1:c.321-14T= NP_001258564.1:n.321-14T=
NM_005444.2:c.321-14T= NP_005435.1:n.321-14T=
NR_073390.1:n.695+1512T=
XM_011512138.1:c.162-14T= XP_011510440.1:n.162-14T=
XM_011512138.3:c.162-14T= XP_011510440.1:n.162-14T=
XM_017005248.1:c.159-14T= XP_016860737.1:n.159-14T=
XM_017005249.2:c.162-14T= XP_016860738.1:n.162-14T=
NM_001271634.2:c.321-14T= NP_001258563.1:n.321-14T=
NM_005444.3:c.321-14T= MANE Select NP_005435.1:n.321-14T=
NR_073390.2:n.436+1512T=
NM_001271635.2:c.321-14T= NP_001258564.1:n.321-14T=