Canonical Allele Identifier: CA431227647

Gene: CNOT9

Linked Data

• MyVariant Identifiers: chr2:g.219447702A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218582979A>G , CM000664.2:g.218582979A>G	GRCh38
NC_000002.11:g.219447702A>G , CM000664.1:g.219447702A>G	GRCh37
NC_000002.10:g.219155946A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273064.11:c.213A>G MANE Select	ENSP00000273064.6:p.Val71=
ENST00000273064.10:c.213A>G	ENSP00000273064.6:p.Val71=
ENST00000295701.9:c.213A>G	ENSP00000295701.5:p.Val71=
ENST00000432877.5:c.*105A>G	ENSP00000392394.1:n.*105A>G
ENST00000542068.5:c.213A>G	ENSP00000443687.1:p.Val71=
ENST00000627282.2:c.213A>G	ENSP00000486540.1:p.Val71=
NM_001271634.1:c.213A>G	NP_001258563.1:p.Val71=
NM_001271635.1:c.213A>G	NP_001258564.1:p.Val71=
NM_005444.2:c.213A>G	NP_005435.1:p.Val71=
NR_073390.1:n.588A>G
XM_011512138.1:c.54A>G	XP_011510440.1:p.Val18=
XM_011512138.3:c.54A>G	XP_011510440.1:p.Val18=
XM_017005248.1:c.51A>G	XP_016860737.1:p.Val17=
XM_017005249.2:c.54A>G	XP_016860738.1:p.Val18=
NM_001271634.2:c.213A>G	NP_001258563.1:p.Val71=
NM_005444.3:c.213A>G MANE Select	NP_005435.1:p.Val71=
NR_073390.2:n.329A>G
NM_001271635.2:c.213A>G	NP_001258564.1:p.Val71=