Canonical Allele Identifier: CA350569220

Gene: CNOT9

Linked Data

• MyVariant Identifiers: chr2:g.219449441A>G (hg19) ; chr2:g.218584718A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218584718A>G , CM000664.2:g.218584718A>G	GRCh38
NC_000002.11:g.219449441A>G , CM000664.1:g.219449441A>G	GRCh37
NC_000002.10:g.219157685A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273064.11:c.427A>G MANE Select	ENSP00000273064.6:p.Ile143Val
ENST00000273064.10:c.427A>G	ENSP00000273064.6:p.Ile143Val
ENST00000295701.9:c.427A>G	ENSP00000295701.5:p.Ile143Val
ENST00000542068.5:c.427A>G	ENSP00000443687.1:p.Ile143Val
ENST00000627282.2:c.427A>G	ENSP00000486540.1:p.Ile143Val
NM_001271634.1:c.427A>G	NP_001258563.1:p.Ile143Val
NM_001271635.1:c.427A>G	NP_001258564.1:p.Ile143Val
NM_005444.2:c.427A>G	NP_005435.1:p.Ile143Val
NR_073390.1:n.695+1632A>G
XM_011512138.1:c.268A>G	XP_011510440.1:p.Ile90Val
XM_011512138.3:c.268A>G	XP_011510440.1:p.Ile90Val
XM_017005248.1:c.265A>G	XP_016860737.1:p.Ile89Val
XM_017005249.2:c.268A>G	XP_016860738.1:p.Ile90Val
NM_001271634.2:c.427A>G	NP_001258563.1:p.Ile143Val
NM_005444.3:c.427A>G MANE Select	NP_005435.1:p.Ile143Val
NR_073390.2:n.436+1632A>G
NM_001271635.2:c.427A>G	NP_001258564.1:p.Ile143Val