Canonical Allele Identifier: CA1328827428

Gene: CNOT9

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218584697C= , CM000664.2:g.218584697C=	GRCh38
NC_000002.11:g.219449420C= , CM000664.1:g.219449420C=	GRCh37
NC_000002.10:g.219157664C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273064.11:c.406C= MANE Select	ENSP00000273064.6:p.Arg136=
ENST00000273064.10:c.406C=	ENSP00000273064.6:p.Arg136=
ENST00000295701.9:c.406C=	ENSP00000295701.5:p.Arg136=
ENST00000542068.5:c.406C=	ENSP00000443687.1:p.Arg136=
ENST00000627282.2:c.406C=	ENSP00000486540.1:p.Arg136=
NM_001271634.1:c.406C=	NP_001258563.1:p.Arg136=
NM_001271635.1:c.406C=	NP_001258564.1:p.Arg136=
NM_005444.2:c.406C=	NP_005435.1:p.Arg136=
NR_073390.1:n.695+1611C=
XM_011512138.1:c.247C=	XP_011510440.1:p.Arg83=
XM_011512138.3:c.247C=	XP_011510440.1:p.Arg83=
XM_017005248.1:c.244C=	XP_016860737.1:p.Arg82=
XM_017005249.2:c.247C=	XP_016860738.1:p.Arg83=
NM_001271634.2:c.406C=	NP_001258563.1:p.Arg136=
NM_005444.3:c.406C= MANE Select	NP_005435.1:p.Arg136=
NR_073390.2:n.436+1611C=
NM_001271635.2:c.406C=	NP_001258564.1:p.Arg136=