Canonical Allele Identifier: CA2577244278

Gene: CNOT9

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218583006_218583009del , CM000664.2:g.218583006_218583009del	GRCh38
NC_000002.11:g.219447729_219447732del , CM000664.1:g.219447729_219447732del	GRCh37
NC_000002.10:g.219155973_219155976del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273064.11:c.240_243del MANE Select	ENSP00000273064.6:p.Thr81Ter
ENST00000273064.10:c.240_243del	ENSP00000273064.6:p.Thr81Ter
ENST00000295701.9:c.240_243del	ENSP00000295701.5:p.Thr81Ter
ENST00000432877.5:c.*132_*135del	ENSP00000392394.1:n.*132_*135del
ENST00000542068.5:c.240_243del	ENSP00000443687.1:p.Thr81Ter
ENST00000627282.2:c.240_243del	ENSP00000486540.1:p.Thr81Ter
NM_001271634.1:c.240_243del	NP_001258563.1:p.Thr81Ter
NM_001271635.1:c.240_243del	NP_001258564.1:p.Thr81Ter
NM_005444.2:c.240_243del	NP_005435.1:p.Thr81Ter
NR_073390.1:n.615_618del
XM_011512138.1:c.81_84del	XP_011510440.1:p.Thr28Ter
XM_011512138.3:c.81_84del	XP_011510440.1:p.Thr28Ter
XM_017005248.1:c.78_81del	XP_016860737.1:p.Thr27Ter
XM_017005249.2:c.81_84del	XP_016860738.1:p.Thr28Ter
NM_001271634.2:c.240_243del	NP_001258563.1:p.Thr81Ter
NM_005444.3:c.240_243del MANE Select	NP_005435.1:p.Thr81Ter
NR_073390.2:n.356_359del
NM_001271635.2:c.240_243del	NP_001258564.1:p.Thr81Ter