Canonical Allele Identifier: CA407758781

Gene: CNOT3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.54143660C>T , CM000681.2:g.54143660C>T	GRCh38
NC_000019.8:g.59339208C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_014516.4:c.169C>T MANE Select	NP_055331.1:p.Arg57Trp
ENST00000221232.11:c.169C>T MANE Select	ENSP00000221232.5:p.Arg57Trp
NM_014516.3:c.169C>T	NP_055331.1:p.Arg57Trp
ENST00000221232.9:c.169C>T	ENSP00000221232.5:p.Arg57Trp
ENST00000358389.7:c.169C>T	ENSP00000351159.4:p.Arg57Trp
ENST00000440571.6:c.169C>T	ENSP00000398463.2:p.Arg57Trp
ENST00000617930.2:c.169C>T	ENSP00000496602.1:p.Arg57Trp
ENST00000618939.4:n.426C>T
ENST00000618939.5:n.451C>T
ENST00000644245.1:c.169C>T	ENSP00000496534.1:p.Arg57Trp
ENST00000646002.1:c.-129-604C>T	ENSP00000495445.1:n.-129-604C>T
XM_005278279.1:c.169C>T	XP_005278336.1:p.Arg57Trp
XM_005278279.2:c.169C>T	XP_005278336.1:p.Arg57Trp
XM_005278280.2:c.169C>T	XP_005278337.1:p.Arg57Trp
XM_005278281.1:c.169C>T	XP_005278338.1:p.Arg57Trp
XM_005278281.2:c.169C>T	XP_005278338.1:p.Arg57Trp
XM_005278282.1:c.169C>T	XP_005278339.1:p.Arg57Trp
XM_005278282.3:c.169C>T	XP_005278339.1:p.Arg57Trp
XM_011526992.1:c.169C>T	XP_011525294.1:p.Arg57Trp
XM_011526992.2:c.169C>T	XP_011525294.1:p.Arg57Trp
XM_011526993.1:c.169C>T	XP_011525295.1:p.Arg57Trp
XM_011526993.3:c.169C>T	XP_011525295.1:p.Arg57Trp
XR_002958318.1:n.464C>T
XR_002958319.1:n.451C>T
XR_254515.1:n.493C>T
XR_254515.3:n.464C>T
XR_254516.3:n.493C>T