Canonical Allele Identifier: CA1328827375

Gene: CNOT9

Linked Data

• dbSNP Id: rs1694526042

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218584523del , CM000664.2:g.218584523del	GRCh38
NC_000002.11:g.219449246del , CM000664.1:g.219449246del	GRCh37
NC_000002.10:g.219157490del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273064.11:c.321-89del MANE Select	ENSP00000273064.6:n.321-89del
ENST00000273064.10:c.321-89del	ENSP00000273064.6:n.321-89del
ENST00000295701.9:c.321-89del	ENSP00000295701.5:n.321-89del
ENST00000432877.5:c.*213-89del	ENSP00000392394.1:n.*213-89del
ENST00000542068.5:c.321-89del	ENSP00000443687.1:n.321-89del
ENST00000627282.2:c.321-89del	ENSP00000486540.1:n.321-89del
NM_001271634.1:c.321-89del	NP_001258563.1:n.321-89del
NM_001271635.1:c.321-89del	NP_001258564.1:n.321-89del
NM_005444.2:c.321-89del	NP_005435.1:n.321-89del
NR_073390.1:n.695+1437del
XM_011512138.1:c.162-89del	XP_011510440.1:n.162-89del
XM_011512138.3:c.162-89del	XP_011510440.1:n.162-89del
XM_017005248.1:c.159-89del	XP_016860737.1:n.159-89del
XM_017005249.2:c.162-89del	XP_016860738.1:n.162-89del
NM_001271634.2:c.321-89del	NP_001258563.1:n.321-89del
NM_005444.3:c.321-89del MANE Select	NP_005435.1:n.321-89del
NR_073390.2:n.436+1437del
NM_001271635.2:c.321-89del	NP_001258564.1:n.321-89del