Canonical Allele Identifier: CA645609878

Gene: CNOT3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.54152474G>A , CM000681.2:g.54152474G>A	GRCh38
NC_000019.8:g.59348023G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_014516.4:c.1752G>A MANE Select	NP_055331.1:p.Pro584=
ENST00000221232.11:c.1752G>A MANE Select	ENSP00000221232.5:p.Pro584=
NM_014516.3:c.1752G>A	NP_055331.1:p.Pro584=
ENST00000221232.9:c.1752G>A	ENSP00000221232.5:p.Pro584=
ENST00000358389.7:c.1752G>A	ENSP00000351159.4:p.Pro584=
ENST00000447684.5:c.1209G>A	ENSP00000411587.2:p.Pro403=
ENST00000457463.1:c.346G>A
ENST00000496327.1:n.176G>A
ENST00000496327.2:c.176G>A
ENST00000613073.4:c.1563G>A
ENST00000617930.2:c.1752G>A	ENSP00000496602.1:p.Pro584=
ENST00000618939.4:n.2265G>A
ENST00000618939.5:n.2290G>A
ENST00000647082.1:c.299+149G>A
XM_005278279.1:c.1755G>A	XP_005278336.1:p.Pro585=
XM_005278279.2:c.1755G>A	XP_005278336.1:p.Pro585=
XM_005278280.2:c.1755G>A	XP_005278337.1:p.Pro585=
XM_005278281.1:c.1752G>A	XP_005278338.1:p.Pro584=
XM_005278281.2:c.1752G>A	XP_005278338.1:p.Pro584=
XM_005278282.1:c.1755G>A	XP_005278339.1:p.Pro585=
XM_005278282.3:c.1755G>A	XP_005278339.1:p.Pro585=
XM_011526992.1:c.1755G>A	XP_011525294.1:p.Pro585=
XM_011526992.2:c.1755G>A	XP_011525294.1:p.Pro585=
XM_011526993.1:c.1755G>A	XP_011525295.1:p.Pro585=
XM_011526993.3:c.1755G>A	XP_011525295.1:p.Pro585=
XR_002958318.1:n.2050G>A
XR_002958319.1:n.2037G>A
XR_254515.1:n.2076G>A
XR_254515.3:n.2047G>A
XR_254516.3:n.2076G>A