Canonical Allele Identifier: CA350568250

Gene: CNOT9

Linked Data

• MyVariant Identifiers: chr2:g.219447773C>T (hg19) ; chr2:g.218583050C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218583050C>T , CM000664.2:g.218583050C>T	GRCh38
NC_000002.11:g.219447773C>T , CM000664.1:g.219447773C>T	GRCh37
NC_000002.10:g.219156017C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273064.11:c.284C>T MANE Select	ENSP00000273064.6:p.Ala95Val
ENST00000273064.10:c.284C>T	ENSP00000273064.6:p.Ala95Val
ENST00000295701.9:c.284C>T	ENSP00000295701.5:p.Ala95Val
ENST00000432877.5:c.*176C>T	ENSP00000392394.1:n.*176C>T
ENST00000542068.5:c.284C>T	ENSP00000443687.1:p.Ala95Val
ENST00000627282.2:c.284C>T	ENSP00000486540.1:p.Ala95Val
NM_001271634.1:c.284C>T	NP_001258563.1:p.Ala95Val
NM_001271635.1:c.284C>T	NP_001258564.1:p.Ala95Val
NM_005444.2:c.284C>T	NP_005435.1:p.Ala95Val
NR_073390.1:n.659C>T
XM_011512138.1:c.125C>T	XP_011510440.1:p.Ala42Val
XM_011512138.3:c.125C>T	XP_011510440.1:p.Ala42Val
XM_017005248.1:c.122C>T	XP_016860737.1:p.Ala41Val
XM_017005249.2:c.125C>T	XP_016860738.1:p.Ala42Val
NM_001271634.2:c.284C>T	NP_001258563.1:p.Ala95Val
NM_005444.3:c.284C>T MANE Select	NP_005435.1:p.Ala95Val
NR_073390.2:n.400C>T
NM_001271635.2:c.284C>T	NP_001258564.1:p.Ala95Val