Canonical Allele Identifier: CA2577244274

Gene: CNOT9

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218582953_218582954del , CM000664.2:g.218582953_218582954del	GRCh38
NC_000002.11:g.219447676_219447677del , CM000664.1:g.219447676_219447677del	GRCh37
NC_000002.10:g.219155920_219155921del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273064.11:c.205-18_205-17del MANE Select	ENSP00000273064.6:n.205-18_205-17del
ENST00000273064.10:c.205-18_205-17del	ENSP00000273064.6:n.205-18_205-17del
ENST00000295701.9:c.205-18_205-17del	ENSP00000295701.5:n.205-18_205-17del
ENST00000432877.5:c.*97-18_*97-17del	ENSP00000392394.1:n.*97-18_*97-17del
ENST00000542068.5:c.205-18_205-17del	ENSP00000443687.1:n.205-18_205-17del
ENST00000627282.2:c.205-18_205-17del	ENSP00000486540.1:n.205-18_205-17del
NM_001271634.1:c.205-18_205-17del	NP_001258563.1:n.205-18_205-17del
NM_001271635.1:c.205-18_205-17del	NP_001258564.1:n.205-18_205-17del
NM_005444.2:c.205-18_205-17del	NP_005435.1:n.205-18_205-17del
NR_073390.1:n.580-18_580-17del
XM_011512138.1:c.46-18_46-17del	XP_011510440.1:n.46-18_46-17del
XM_011512138.3:c.46-18_46-17del	XP_011510440.1:n.46-18_46-17del
XM_017005248.1:c.43-18_43-17del	XP_016860737.1:n.43-18_43-17del
XM_017005249.2:c.46-18_46-17del	XP_016860738.1:n.46-18_46-17del
NM_001271634.2:c.205-18_205-17del	NP_001258563.1:n.205-18_205-17del
NM_005444.3:c.205-18_205-17del MANE Select	NP_005435.1:n.205-18_205-17del
NR_073390.2:n.321-18_321-17del
NM_001271635.2:c.205-18_205-17del	NP_001258564.1:n.205-18_205-17del