Canonical Allele Identifier: CA915953008
Gene: CNOT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.54145938del , CM000681.2:g.54145938del GRCh38

Transcript Alleles

HGVS Amino-acid Change
NM_014516.4:c.732del MANE Select NP_055331.1:p.Ser245AlafsTer?
ENST00000221232.11:c.732del MANE Select ENSP00000221232.5:p.Ser245AlafsTer?
NM_014516.3:c.732del NP_055331.1:p.Ser245AlafsTer?
ENST00000221232.9:c.732del ENSP00000221232.5:p.Ser245AlafsTer?
ENST00000358389.7:c.732del ENSP00000351159.4:p.Ser245AlafsTer?
ENST00000440571.5:c.497del
ENST00000440571.6:c.735del ENSP00000398463.2:p.Ser246AlafsTer?
ENST00000447684.5:c.189del ENSP00000411587.2:p.Ser64AlafsTer?
ENST00000613073.4:c.543del
ENST00000617930.2:c.732del ENSP00000496602.1:p.Ser245AlafsTer?
ENST00000618939.4:n.1245del
ENST00000618939.5:n.1270del
XM_005278279.1:c.735del XP_005278336.1:p.Ser246AlafsTer?
XM_005278279.2:c.735del XP_005278336.1:p.Ser246AlafsTer?
XM_005278280.2:c.735del XP_005278337.1:p.Ser246AlafsTer?
XM_005278281.1:c.732del XP_005278338.1:p.Ser245AlafsTer?
XM_005278281.2:c.732del XP_005278338.1:p.Ser245AlafsTer?
XM_005278282.1:c.735del XP_005278339.1:p.Ser246AlafsTer?
XM_005278282.3:c.735del XP_005278339.1:p.Ser246AlafsTer?
XM_011526992.1:c.735del XP_011525294.1:p.Ser246AlafsTer?
XM_011526992.2:c.735del XP_011525294.1:p.Ser246AlafsTer?
XM_011526993.1:c.735del XP_011525295.1:p.Ser246AlafsTer?
XM_011526993.3:c.735del XP_011525295.1:p.Ser246AlafsTer?
XR_002958318.1:n.1030del
XR_002958319.1:n.1017del
XR_254515.1:n.1056del
XR_254515.3:n.1027del
XR_254516.3:n.1056del