Canonical Allele Identifier: CA350567977

Gene: CNOT9

Linked Data

• MyVariant Identifiers: chr2:g.219447727C>A (hg19) ; chr2:g.218583004C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218583004C>A , CM000664.2:g.218583004C>A	GRCh38
NC_000002.11:g.219447727C>A , CM000664.1:g.219447727C>A	GRCh37
NC_000002.10:g.219155971C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273064.11:c.238C>A MANE Select	ENSP00000273064.6:p.Pro80Thr
ENST00000273064.10:c.238C>A	ENSP00000273064.6:p.Pro80Thr
ENST00000295701.9:c.238C>A	ENSP00000295701.5:p.Pro80Thr
ENST00000432877.5:c.*130C>A	ENSP00000392394.1:n.*130C>A
ENST00000542068.5:c.238C>A	ENSP00000443687.1:p.Pro80Thr
ENST00000627282.2:c.238C>A	ENSP00000486540.1:p.Pro80Thr
NM_001271634.1:c.238C>A	NP_001258563.1:p.Pro80Thr
NM_001271635.1:c.238C>A	NP_001258564.1:p.Pro80Thr
NM_005444.2:c.238C>A	NP_005435.1:p.Pro80Thr
NR_073390.1:n.613C>A
XM_011512138.1:c.79C>A	XP_011510440.1:p.Pro27Thr
XM_011512138.3:c.79C>A	XP_011510440.1:p.Pro27Thr
XM_017005248.1:c.76C>A	XP_016860737.1:p.Pro26Thr
XM_017005249.2:c.79C>A	XP_016860738.1:p.Pro27Thr
NM_001271634.2:c.238C>A	NP_001258563.1:p.Pro80Thr
NM_005444.3:c.238C>A MANE Select	NP_005435.1:p.Pro80Thr
NR_073390.2:n.354C>A
NM_001271635.2:c.238C>A	NP_001258564.1:p.Pro80Thr