Canonical Allele Identifier: CA350569134

Gene: CNOT9

Linked Data

• MyVariant Identifiers: chr2:g.219449400C>G (hg19) ; chr2:g.218584677C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218584677C>G , CM000664.2:g.218584677C>G	GRCh38
NC_000002.11:g.219449400C>G , CM000664.1:g.219449400C>G	GRCh37
NC_000002.10:g.219157644C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273064.11:c.386C>G MANE Select	ENSP00000273064.6:p.Thr129Arg
ENST00000273064.10:c.386C>G	ENSP00000273064.6:p.Thr129Arg
ENST00000295701.9:c.386C>G	ENSP00000295701.5:p.Thr129Arg
ENST00000542068.5:c.386C>G	ENSP00000443687.1:p.Thr129Arg
ENST00000627282.2:c.386C>G	ENSP00000486540.1:p.Thr129Arg
NM_001271634.1:c.386C>G	NP_001258563.1:p.Thr129Arg
NM_001271635.1:c.386C>G	NP_001258564.1:p.Thr129Arg
NM_005444.2:c.386C>G	NP_005435.1:p.Thr129Arg
NR_073390.1:n.695+1591C>G
XM_011512138.1:c.227C>G	XP_011510440.1:p.Thr76Arg
XM_011512138.3:c.227C>G	XP_011510440.1:p.Thr76Arg
XM_017005248.1:c.224C>G	XP_016860737.1:p.Thr75Arg
XM_017005249.2:c.227C>G	XP_016860738.1:p.Thr76Arg
NM_001271634.2:c.386C>G	NP_001258563.1:p.Thr129Arg
NM_005444.3:c.386C>G MANE Select	NP_005435.1:p.Thr129Arg
NR_073390.2:n.436+1591C>G
NM_001271635.2:c.386C>G	NP_001258564.1:p.Thr129Arg