Canonical Allele Identifier: CA2508404758

Gene: CNOT9

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218584581_218584582insA , CM000664.2:g.218584581_218584582insA	GRCh38
NC_000002.11:g.219449304_219449305insA , CM000664.1:g.219449304_219449305insA	GRCh37
NC_000002.10:g.219157548_219157549insA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273064.11:c.321-31_321-30insA MANE Select	ENSP00000273064.6:n.321-31_321-30insA
ENST00000273064.10:c.321-31_321-30insA	ENSP00000273064.6:n.321-31_321-30insA
ENST00000295701.9:c.321-31_321-30insA	ENSP00000295701.5:n.321-31_321-30insA
ENST00000432877.5:c.*213-31_*213-30insA	ENSP00000392394.1:n.*213-31_*213-30insA
ENST00000542068.5:c.321-31_321-30insA	ENSP00000443687.1:n.321-31_321-30insA
ENST00000627282.2:c.321-31_321-30insA	ENSP00000486540.1:n.321-31_321-30insA
NM_001271634.1:c.321-31_321-30insA	NP_001258563.1:n.321-31_321-30insA
NM_001271635.1:c.321-31_321-30insA	NP_001258564.1:n.321-31_321-30insA
NM_005444.2:c.321-31_321-30insA	NP_005435.1:n.321-31_321-30insA
NR_073390.1:n.695+1495_695+1496insA
XM_011512138.1:c.162-31_162-30insA	XP_011510440.1:n.162-31_162-30insA
XM_011512138.3:c.162-31_162-30insA	XP_011510440.1:n.162-31_162-30insA
XM_017005248.1:c.159-31_159-30insA	XP_016860737.1:n.159-31_159-30insA
XM_017005249.2:c.162-31_162-30insA	XP_016860738.1:n.162-31_162-30insA
NM_001271634.2:c.321-31_321-30insA	NP_001258563.1:n.321-31_321-30insA
NM_005444.3:c.321-31_321-30insA MANE Select	NP_005435.1:n.321-31_321-30insA
NR_073390.2:n.436+1495_436+1496insA
NM_001271635.2:c.321-31_321-30insA	NP_001258564.1:n.321-31_321-30insA