Canonical Allele Identifier: CA1328827414

Gene: CNOT9

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218584644T= , CM000664.2:g.218584644T=	GRCh38
NC_000002.11:g.219449367T= , CM000664.1:g.219449367T=	GRCh37
NC_000002.10:g.219157611T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273064.11:c.353T= MANE Select	ENSP00000273064.6:p.Phe118=
ENST00000273064.10:c.353T=	ENSP00000273064.6:p.Phe118=
ENST00000295701.9:c.353T=	ENSP00000295701.5:p.Phe118=
ENST00000432877.5:c.*245T=	ENSP00000392394.1:n.*245T=
ENST00000542068.5:c.353T=	ENSP00000443687.1:p.Phe118=
ENST00000627282.2:c.353T=	ENSP00000486540.1:p.Phe118=
NM_001271634.1:c.353T=	NP_001258563.1:p.Phe118=
NM_001271635.1:c.353T=	NP_001258564.1:p.Phe118=
NM_005444.2:c.353T=	NP_005435.1:p.Phe118=
NR_073390.1:n.695+1558T=
XM_011512138.1:c.194T=	XP_011510440.1:p.Phe65=
XM_011512138.3:c.194T=	XP_011510440.1:p.Phe65=
XM_017005248.1:c.191T=	XP_016860737.1:p.Phe64=
XM_017005249.2:c.194T=	XP_016860738.1:p.Phe65=
NM_001271634.2:c.353T=	NP_001258563.1:p.Phe118=
NM_005444.3:c.353T= MANE Select	NP_005435.1:p.Phe118=
NR_073390.2:n.436+1558T=
NM_001271635.2:c.353T=	NP_001258564.1:p.Phe118=