Canonical Allele Identifier: CA645517062

Gene: CNOT9

Linked Data

• COSMIC: COSM5396211

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218584682_218584683delinsTT , CM000664.2:g.218584682_218584683delinsTT	GRCh38
NC_000002.11:g.219449405_219449406delinsTT , CM000664.1:g.219449405_219449406delinsTT	GRCh37
NC_000002.10:g.219157649_219157650delinsTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273064.11:c.391_392delinsTT MANE Select	ENSP00000273064.6:p.Pro131Phe
ENST00000273064.10:c.391_392delinsTT	ENSP00000273064.6:p.Pro131Phe
ENST00000295701.9:c.391_392delinsTT	ENSP00000295701.5:p.Pro131Phe
ENST00000542068.5:c.391_392delinsTT	ENSP00000443687.1:p.Pro131Phe
ENST00000627282.2:c.391_392delinsTT	ENSP00000486540.1:p.Pro131Phe
NM_001271634.1:c.391_392delinsTT	NP_001258563.1:p.Pro131Phe
NM_001271635.1:c.391_392delinsTT	NP_001258564.1:p.Pro131Phe
NM_005444.2:c.391_392delinsTT	NP_005435.1:p.Pro131Phe
NR_073390.1:n.695+1596_695+1597delinsTT
XM_011512138.1:c.232_233delinsTT	XP_011510440.1:p.Pro78Phe
XM_011512138.3:c.232_233delinsTT	XP_011510440.1:p.Pro78Phe
XM_017005248.1:c.229_230delinsTT	XP_016860737.1:p.Pro77Phe
XM_017005249.2:c.232_233delinsTT	XP_016860738.1:p.Pro78Phe
NM_001271634.2:c.391_392delinsTT	NP_001258563.1:p.Pro131Phe
NM_005444.3:c.391_392delinsTT MANE Select	NP_005435.1:p.Pro131Phe
NR_073390.2:n.436+1596_436+1597delinsTT
NM_001271635.2:c.391_392delinsTT	NP_001258564.1:p.Pro131Phe