Canonical Allele Identifier: CA1328827413

Gene: CNOT9

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218584640_218584641delinsCT , CM000664.2:g.218584640_218584641delinsCT	GRCh38
NC_000002.11:g.219449363_219449364delinsCT , CM000664.1:g.219449363_219449364delinsCT	GRCh37
NC_000002.10:g.219157607_219157608delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273064.11:c.349_350delinsCT MANE Select	ENSP00000273064.6:p.Leu117=
ENST00000273064.10:c.349_350delinsCT	ENSP00000273064.6:p.Leu117=
ENST00000295701.9:c.349_350delinsCT	ENSP00000295701.5:p.Leu117=
ENST00000432877.5:c.*241_*242delinsCT	ENSP00000392394.1:n.*241_*242delinsCT
ENST00000542068.5:c.349_350delinsCT	ENSP00000443687.1:p.Leu117=
ENST00000627282.2:c.349_350delinsCT	ENSP00000486540.1:p.Leu117=
NM_001271634.1:c.349_350delinsCT	NP_001258563.1:p.Leu117=
NM_001271635.1:c.349_350delinsCT	NP_001258564.1:p.Leu117=
NM_005444.2:c.349_350delinsCT	NP_005435.1:p.Leu117=
NR_073390.1:n.695+1554_695+1555delinsCT
XM_011512138.1:c.190_191delinsCT	XP_011510440.1:p.Leu64=
XM_011512138.3:c.190_191delinsCT	XP_011510440.1:p.Leu64=
XM_017005248.1:c.187_188delinsCT	XP_016860737.1:p.Leu63=
XM_017005249.2:c.190_191delinsCT	XP_016860738.1:p.Leu64=
NM_001271634.2:c.349_350delinsCT	NP_001258563.1:p.Leu117=
NM_005444.3:c.349_350delinsCT MANE Select	NP_005435.1:p.Leu117=
NR_073390.2:n.436+1554_436+1555delinsCT
NM_001271635.2:c.349_350delinsCT	NP_001258564.1:p.Leu117=