Canonical Allele Identifier: CA1328827374

Gene: CNOT9

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218584521_218584522delinsGC , CM000664.2:g.218584521_218584522delinsGC	GRCh38
NC_000002.11:g.219449244_219449245delinsGC , CM000664.1:g.219449244_219449245delinsGC	GRCh37
NC_000002.10:g.219157488_219157489delinsGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273064.11:c.321-91_321-90delinsGC MANE Select	ENSP00000273064.6:n.321-91_321-90delinsGC
ENST00000273064.10:c.321-91_321-90delinsGC	ENSP00000273064.6:n.321-91_321-90delinsGC
ENST00000295701.9:c.321-91_321-90delinsGC	ENSP00000295701.5:n.321-91_321-90delinsGC
ENST00000432877.5:c.*213-91_*213-90delinsGC	ENSP00000392394.1:n.*213-91_*213-90delinsGC
ENST00000542068.5:c.321-91_321-90delinsGC	ENSP00000443687.1:n.321-91_321-90delinsGC
ENST00000627282.2:c.321-91_321-90delinsGC	ENSP00000486540.1:n.321-91_321-90delinsGC
NM_001271634.1:c.321-91_321-90delinsGC	NP_001258563.1:n.321-91_321-90delinsGC
NM_001271635.1:c.321-91_321-90delinsGC	NP_001258564.1:n.321-91_321-90delinsGC
NM_005444.2:c.321-91_321-90delinsGC	NP_005435.1:n.321-91_321-90delinsGC
NR_073390.1:n.695+1435_695+1436delinsGC
XM_011512138.1:c.162-91_162-90delinsGC	XP_011510440.1:n.162-91_162-90delinsGC
XM_011512138.3:c.162-91_162-90delinsGC	XP_011510440.1:n.162-91_162-90delinsGC
XM_017005248.1:c.159-91_159-90delinsGC	XP_016860737.1:n.159-91_159-90delinsGC
XM_017005249.2:c.162-91_162-90delinsGC	XP_016860738.1:n.162-91_162-90delinsGC
NM_001271634.2:c.321-91_321-90delinsGC	NP_001258563.1:n.321-91_321-90delinsGC
NM_005444.3:c.321-91_321-90delinsGC MANE Select	NP_005435.1:n.321-91_321-90delinsGC
NR_073390.2:n.436+1435_436+1436delinsGC
NM_001271635.2:c.321-91_321-90delinsGC	NP_001258564.1:n.321-91_321-90delinsGC