Canonical Allele Identifier: CA431228447

Gene: CNOT9

Linked Data

• MyVariant Identifiers: chr2:g.219449380T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218584657T>C , CM000664.2:g.218584657T>C	GRCh38
NC_000002.11:g.219449380T>C , CM000664.1:g.219449380T>C	GRCh37
NC_000002.10:g.219157624T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273064.11:c.366T>C MANE Select	ENSP00000273064.6:p.Phe122=
ENST00000273064.10:c.366T>C	ENSP00000273064.6:p.Phe122=
ENST00000295701.9:c.366T>C	ENSP00000295701.5:p.Phe122=
ENST00000542068.5:c.366T>C	ENSP00000443687.1:p.Phe122=
ENST00000627282.2:c.366T>C	ENSP00000486540.1:p.Phe122=
NM_001271634.1:c.366T>C	NP_001258563.1:p.Phe122=
NM_001271635.1:c.366T>C	NP_001258564.1:p.Phe122=
NM_005444.2:c.366T>C	NP_005435.1:p.Phe122=
NR_073390.1:n.695+1571T>C
XM_011512138.1:c.207T>C	XP_011510440.1:p.Phe69=
XM_011512138.3:c.207T>C	XP_011510440.1:p.Phe69=
XM_017005248.1:c.204T>C	XP_016860737.1:p.Phe68=
XM_017005249.2:c.207T>C	XP_016860738.1:p.Phe69=
NM_001271634.2:c.366T>C	NP_001258563.1:p.Phe122=
NM_005444.3:c.366T>C MANE Select	NP_005435.1:p.Phe122=
NR_073390.2:n.436+1571T>C
NM_001271635.2:c.366T>C	NP_001258564.1:p.Phe122=