Canonical Allele Identifier: CA1328827425
Gene: CNOT9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218584683C= , CM000664.2:g.218584683C= GRCh38
NC_000002.11:g.219449406C= , CM000664.1:g.219449406C= GRCh37
NC_000002.10:g.219157650C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000273064.11:c.392C= MANE Select ENSP00000273064.6:p.Pro131=
ENST00000273064.10:c.392C= ENSP00000273064.6:p.Pro131=
ENST00000295701.9:c.392C= ENSP00000295701.5:p.Pro131=
ENST00000542068.5:c.392C= ENSP00000443687.1:p.Pro131=
ENST00000627282.2:c.392C= ENSP00000486540.1:p.Pro131=
NM_001271634.1:c.392C= NP_001258563.1:p.Pro131=
NM_001271635.1:c.392C= NP_001258564.1:p.Pro131=
NM_005444.2:c.392C= NP_005435.1:p.Pro131=
NR_073390.1:n.695+1597C=
XM_011512138.1:c.233C= XP_011510440.1:p.Pro78=
XM_011512138.3:c.233C= XP_011510440.1:p.Pro78=
XM_017005248.1:c.230C= XP_016860737.1:p.Pro77=
XM_017005249.2:c.233C= XP_016860738.1:p.Pro78=
NM_001271634.2:c.392C= NP_001258563.1:p.Pro131=
NM_005444.3:c.392C= MANE Select NP_005435.1:p.Pro131=
NR_073390.2:n.436+1597C=
NM_001271635.2:c.392C= NP_001258564.1:p.Pro131=