Canonical Allele Identifier: CA431227737

Gene: CNOT9

Linked Data

• gnomAD v4: 2-218583015-A-C
• MyVariant Identifiers: chr2:g.219447738A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218583015A>C , CM000664.2:g.218583015A>C	GRCh38
NC_000002.11:g.219447738A>C , CM000664.1:g.219447738A>C	GRCh37
NC_000002.10:g.219155982A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273064.11:c.249A>C MANE Select	ENSP00000273064.6:p.Thr83=
ENST00000273064.10:c.249A>C	ENSP00000273064.6:p.Thr83=
ENST00000295701.9:c.249A>C	ENSP00000295701.5:p.Thr83=
ENST00000432877.5:c.*141A>C	ENSP00000392394.1:n.*141A>C
ENST00000542068.5:c.249A>C	ENSP00000443687.1:p.Thr83=
ENST00000627282.2:c.249A>C	ENSP00000486540.1:p.Thr83=
NM_001271634.1:c.249A>C	NP_001258563.1:p.Thr83=
NM_001271635.1:c.249A>C	NP_001258564.1:p.Thr83=
NM_005444.2:c.249A>C	NP_005435.1:p.Thr83=
NR_073390.1:n.624A>C
XM_011512138.1:c.90A>C	XP_011510440.1:p.Thr30=
XM_011512138.3:c.90A>C	XP_011510440.1:p.Thr30=
XM_017005248.1:c.87A>C	XP_016860737.1:p.Thr29=
XM_017005249.2:c.90A>C	XP_016860738.1:p.Thr30=
NM_001271634.2:c.249A>C	NP_001258563.1:p.Thr83=
NM_005444.3:c.249A>C MANE Select	NP_005435.1:p.Thr83=
NR_073390.2:n.365A>C
NM_001271635.2:c.249A>C	NP_001258564.1:p.Thr83=