Canonical Allele Identifier: CA1328827432

Gene: CNOT9

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218584732A= , CM000664.2:g.218584732A=	GRCh38
NC_000002.11:g.219449455A= , CM000664.1:g.219449455A=	GRCh37
NC_000002.10:g.219157699A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273064.11:c.430+11A= MANE Select	ENSP00000273064.6:n.430+11A=
ENST00000273064.10:c.430+11A=	ENSP00000273064.6:n.430+11A=
ENST00000295701.9:c.430+11A=	ENSP00000295701.5:n.430+11A=
ENST00000542068.5:c.430+11A=	ENSP00000443687.1:n.430+11A=
ENST00000627282.2:c.430+11A=	ENSP00000486540.1:n.430+11A=
NM_001271634.1:c.430+11A=	NP_001258563.1:n.430+11A=
NM_001271635.1:c.430+11A=	NP_001258564.1:n.430+11A=
NM_005444.2:c.430+11A=	NP_005435.1:n.430+11A=
NR_073390.1:n.695+1646A=
XM_011512138.1:c.271+11A=	XP_011510440.1:n.271+11A=
XM_011512138.3:c.271+11A=	XP_011510440.1:n.271+11A=
XM_017005248.1:c.268+11A=	XP_016860737.1:n.268+11A=
XM_017005249.2:c.271+11A=	XP_016860738.1:n.271+11A=
NM_001271634.2:c.430+11A=	NP_001258563.1:n.430+11A=
NM_005444.3:c.430+11A= MANE Select	NP_005435.1:n.430+11A=
NR_073390.2:n.436+1646A=
NM_001271635.2:c.430+11A=	NP_001258564.1:n.430+11A=