Canonical Allele Identifier: CA350567795

Gene: CNOT9

Linked Data

• MyVariant Identifiers: chr2:g.219447698T>C (hg19) ; chr2:g.218582975T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218582975T>C , CM000664.2:g.218582975T>C	GRCh38
NC_000002.11:g.219447698T>C , CM000664.1:g.219447698T>C	GRCh37
NC_000002.10:g.219155942T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273064.11:c.209T>C MANE Select	ENSP00000273064.6:p.Ile70Thr
ENST00000273064.10:c.209T>C	ENSP00000273064.6:p.Ile70Thr
ENST00000295701.9:c.209T>C	ENSP00000295701.5:p.Ile70Thr
ENST00000432877.5:c.*101T>C	ENSP00000392394.1:n.*101T>C
ENST00000542068.5:c.209T>C	ENSP00000443687.1:p.Ile70Thr
ENST00000627282.2:c.209T>C	ENSP00000486540.1:p.Ile70Thr
NM_001271634.1:c.209T>C	NP_001258563.1:p.Ile70Thr
NM_001271635.1:c.209T>C	NP_001258564.1:p.Ile70Thr
NM_005444.2:c.209T>C	NP_005435.1:p.Ile70Thr
NR_073390.1:n.584T>C
XM_011512138.1:c.50T>C	XP_011510440.1:p.Ile17Thr
XM_011512138.3:c.50T>C	XP_011510440.1:p.Ile17Thr
XM_017005248.1:c.47T>C	XP_016860737.1:p.Ile16Thr
XM_017005249.2:c.50T>C	XP_016860738.1:p.Ile17Thr
NM_001271634.2:c.209T>C	NP_001258563.1:p.Ile70Thr
NM_005444.3:c.209T>C MANE Select	NP_005435.1:p.Ile70Thr
NR_073390.2:n.325T>C
NM_001271635.2:c.209T>C	NP_001258564.1:p.Ile70Thr