Canonical Allele Identifier: CA407763197

Gene: CNOT3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.54148196C>G , CM000681.2:g.54148196C>G	GRCh38
NC_000019.8:g.59343743C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_014516.4:c.943C>G MANE Select	NP_055331.1:p.Gln315Glu
ENST00000221232.11:c.943C>G MANE Select	ENSP00000221232.5:p.Gln315Glu
NM_014516.3:c.943C>G	NP_055331.1:p.Gln315Glu
ENST00000221232.9:c.943C>G	ENSP00000221232.5:p.Gln315Glu
ENST00000358389.7:c.943C>G	ENSP00000351159.4:p.Gln315Glu
ENST00000440571.5:c.708C>G
ENST00000440571.6:c.946C>G	ENSP00000398463.2:p.Gln316Glu
ENST00000447684.5:c.400C>G	ENSP00000411587.2:p.Gln134Glu
ENST00000613073.4:c.754C>G
ENST00000617930.2:c.943C>G	ENSP00000496602.1:p.Gln315Glu
ENST00000618939.4:n.1456C>G
ENST00000618939.5:n.1481C>G
XM_005278279.1:c.946C>G	XP_005278336.1:p.Gln316Glu
XM_005278279.2:c.946C>G	XP_005278336.1:p.Gln316Glu
XM_005278280.2:c.946C>G	XP_005278337.1:p.Gln316Glu
XM_005278281.1:c.943C>G	XP_005278338.1:p.Gln315Glu
XM_005278281.2:c.943C>G	XP_005278338.1:p.Gln315Glu
XM_005278282.1:c.946C>G	XP_005278339.1:p.Gln316Glu
XM_005278282.3:c.946C>G	XP_005278339.1:p.Gln316Glu
XM_011526992.1:c.946C>G	XP_011525294.1:p.Gln316Glu
XM_011526992.2:c.946C>G	XP_011525294.1:p.Gln316Glu
XM_011526993.1:c.946C>G	XP_011525295.1:p.Gln316Glu
XM_011526993.3:c.946C>G	XP_011525295.1:p.Gln316Glu
XR_001754001.2:n.963+832G>C
XR_002958318.1:n.1241C>G
XR_002958319.1:n.1228C>G
XR_254515.1:n.1267C>G
XR_254515.3:n.1238C>G
XR_254516.3:n.1267C>G
XR_430258.2:n.1376-637G>C
XR_936070.1:n.1375+832G>C