Canonical Allele Identifier: CA2298023

Gene: CNOT10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.32713347A>G , CM000665.2:g.32713347A>G	GRCh38
NC_000003.11:g.32754839A>G , CM000665.1:g.32754839A>G	GRCh37
NC_000003.10:g.32729843A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328834.10:c.551A>G MANE Select	ENSP00000330060.5:p.Asn184Ser
ENST00000454516.7:c.731A>G	ENSP00000399862.2:p.Asn244Ser
ENST00000328834.9:c.551A>G	ENSP00000330060.5:p.Asn184Ser
ENST00000331889.10:c.551A>G	ENSP00000329376.6:p.Asn184Ser
ENST00000416457.5:c.427A>G
ENST00000435630.5:c.389A>G	ENSP00000402795.1:p.Asn130Ser
ENST00000454516.6:c.731A>G	ENSP00000399862.2:p.Asn244Ser
ENST00000455381.5:c.125-2878A>G	ENSP00000392312.1:n.125-2878A>G
ENST00000485136.5:n.606A>G
ENST00000494439.5:n.442A>G
ENST00000556853.5:n.442A>G
NM_001256741.1:c.551A>G	NP_001243670.1:p.Asn184Ser
NM_001256742.1:c.731A>G	NP_001243671.1:p.Asn244Ser
NM_015442.2:c.551A>G	NP_056257.1:p.Asn184Ser
NR_046352.1:n.705A>G
XM_006713084.2:c.731A>G	XP_006713147.1:p.Asn244Ser
XM_006713085.2:c.731A>G	XP_006713148.1:p.Asn244Ser
XM_011533566.1:c.731A>G	XP_011531868.1:p.Asn244Ser
XM_011533569.1:c.731A>G	XP_011531871.1:p.Asn244Ser
XR_940404.1:n.811A>G
XM_006713084.3:c.731A>G	XP_006713147.1:p.Asn244Ser
XM_006713085.3:c.731A>G	XP_006713148.1:p.Asn244Ser
XM_011533566.2:c.731A>G	XP_011531868.1:p.Asn244Ser
XM_017006109.2:c.551A>G	XP_016861598.1:p.Asn184Ser
XM_017006110.2:c.551A>G	XP_016861599.1:p.Asn184Ser
XM_017006111.2:c.551A>G	XP_016861600.1:p.Asn184Ser
XM_017006112.2:c.551A>G	XP_016861601.1:p.Asn184Ser
XR_001740089.1:n.824A>G
NM_001256741.2:c.551A>G	NP_001243670.1:p.Asn184Ser
NM_015442.3:c.551A>G MANE Select	NP_056257.1:p.Asn184Ser
NR_046352.2:n.662A>G
NM_001256742.2:c.731A>G	NP_001243671.1:p.Asn244Ser
NM_001393366.1:c.551A>G	NP_001380295.1:p.Asn184Ser
NM_001393367.1:c.551A>G	NP_001380296.1:p.Asn184Ser
NM_001393368.1:c.551A>G	NP_001380297.1:p.Asn184Ser
NM_001393369.1:c.551A>G	NP_001380298.1:p.Asn184Ser