Canonical Allele Identifier: CA2298282

Gene: CNOT10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.32737438A>G , CM000665.2:g.32737438A>G	GRCh38
NC_000003.11:g.32778930A>G , CM000665.1:g.32778930A>G	GRCh37
NC_000003.10:g.32753934A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328834.10:c.1543A>G MANE Select	ENSP00000330060.5:p.Ile515Val
ENST00000454516.7:c.1723A>G	ENSP00000399862.2:p.Ile575Val
ENST00000328834.9:c.1543A>G	ENSP00000330060.5:p.Ile515Val
ENST00000331889.10:c.1514+2462A>G	ENSP00000329376.6:n.1514+2462A>G
ENST00000416457.5:c.1301A>G
ENST00000430408.1:c.184A>G	ENSP00000395385.1:p.Ile62Val
ENST00000435630.5:c.1352+2462A>G	ENSP00000402795.1:n.1352+2462A>G
ENST00000454516.6:c.1723A>G	ENSP00000399862.2:p.Ile575Val
NM_001256741.1:c.1514+2462A>G	NP_001243670.1:n.1514+2462A>G
NM_001256742.1:c.1723A>G	NP_001243671.1:p.Ile575Val
NM_015442.2:c.1543A>G	NP_056257.1:p.Ile515Val
NR_046352.1:n.1668+2462A>G
XM_006713084.2:c.1720A>G	XP_006713147.1:p.Ile574Val
XM_006713085.2:c.1723A>G	XP_006713148.1:p.Ile575Val
XM_011533566.1:c.1694+2462A>G	XP_011531868.1:n.1694+2462A>G
XM_011533567.1:c.859A>G	XP_011531869.1:p.Ile287Val
XM_011533568.1:c.577A>G	XP_011531870.1:p.Ile193Val
XR_940404.1:n.1803A>G
XM_006713084.3:c.1720A>G	XP_006713147.1:p.Ile574Val
XM_006713085.3:c.1723A>G	XP_006713148.1:p.Ile575Val
XM_011533566.2:c.1694+2462A>G	XP_011531868.1:n.1694+2462A>G
XM_011533567.2:c.859A>G	XP_011531869.1:p.Ile287Val
XM_017006109.2:c.1540A>G	XP_016861598.1:p.Ile514Val
XM_017006110.2:c.1543A>G	XP_016861599.1:p.Ile515Val
XM_017006111.2:c.1540A>G	XP_016861600.1:p.Ile514Val
XM_017006112.2:c.1514+2462A>G	XP_016861601.1:n.1514+2462A>G
XR_001740089.1:n.1816A>G
NM_001256741.2:c.1514+2462A>G	NP_001243670.1:n.1514+2462A>G
NM_015442.3:c.1543A>G MANE Select	NP_056257.1:p.Ile515Val
NR_046352.2:n.1625+2462A>G
NM_001256742.2:c.1723A>G	NP_001243671.1:p.Ile575Val
NM_001393366.1:c.1540A>G	NP_001380295.1:p.Ile514Val
NM_001393367.1:c.1543A>G	NP_001380296.1:p.Ile515Val
NM_001393368.1:c.1540A>G	NP_001380297.1:p.Ile514Val
NM_001393369.1:c.1514+2462A>G	NP_001380298.1:n.1514+2462A>G