Canonical Allele Identifier: CA2297977

Gene: CNOT10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.32708742G>A , CM000665.2:g.32708742G>A	GRCh38
NC_000003.11:g.32750234G>A , CM000665.1:g.32750234G>A	GRCh37
NC_000003.10:g.32725238G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328834.10:c.352G>A MANE Select	ENSP00000330060.5:p.Val118Ile
ENST00000454516.7:c.532G>A	ENSP00000399862.2:p.Val178Ile
ENST00000328834.9:c.352G>A	ENSP00000330060.5:p.Val118Ile
ENST00000331889.10:c.352G>A	ENSP00000329376.6:p.Val118Ile
ENST00000416457.5:c.228G>A
ENST00000435630.5:c.190G>A	ENSP00000402795.1:p.Val64Ile
ENST00000454516.6:c.532G>A	ENSP00000399862.2:p.Val178Ile
ENST00000455381.5:c.46G>A	ENSP00000392312.1:p.Val16Ile
ENST00000463006.5:n.617G>A
ENST00000466103.1:n.270G>A
ENST00000485136.5:n.407G>A
ENST00000494439.5:n.243G>A
ENST00000556853.5:n.243G>A
NM_001256741.1:c.352G>A	NP_001243670.1:p.Val118Ile
NM_001256742.1:c.532G>A	NP_001243671.1:p.Val178Ile
NM_015442.2:c.352G>A	NP_056257.1:p.Val118Ile
NR_046352.1:n.506G>A
XM_006713084.2:c.532G>A	XP_006713147.1:p.Val178Ile
XM_006713085.2:c.532G>A	XP_006713148.1:p.Val178Ile
XM_011533566.1:c.532G>A	XP_011531868.1:p.Val178Ile
XM_011533569.1:c.532G>A	XP_011531871.1:p.Val178Ile
XR_940404.1:n.612G>A
XM_006713084.3:c.532G>A	XP_006713147.1:p.Val178Ile
XM_006713085.3:c.532G>A	XP_006713148.1:p.Val178Ile
XM_011533566.2:c.532G>A	XP_011531868.1:p.Val178Ile
XM_017006109.2:c.352G>A	XP_016861598.1:p.Val118Ile
XM_017006110.2:c.352G>A	XP_016861599.1:p.Val118Ile
XM_017006111.2:c.352G>A	XP_016861600.1:p.Val118Ile
XM_017006112.2:c.352G>A	XP_016861601.1:p.Val118Ile
XR_001740089.1:n.625G>A
NM_001256741.2:c.352G>A	NP_001243670.1:p.Val118Ile
NM_015442.3:c.352G>A MANE Select	NP_056257.1:p.Val118Ile
NR_046352.2:n.463G>A
NM_001256742.2:c.532G>A	NP_001243671.1:p.Val178Ile
NM_001393366.1:c.352G>A	NP_001380295.1:p.Val118Ile
NM_001393367.1:c.352G>A	NP_001380296.1:p.Val118Ile
NM_001393368.1:c.352G>A	NP_001380297.1:p.Val118Ile
NM_001393369.1:c.352G>A	NP_001380298.1:p.Val118Ile