Canonical Allele Identifier: CA2580574602
Gene: CNOT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.54146027_54146031dup , CM000681.2:g.54146027_54146031dup GRCh38
NC_000019.8:g.59341575_59341579dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_014516.4:c.821_825dup MANE Select NP_055331.1:p.Asn276GlnfsTer?
ENST00000221232.11:c.821_825dup MANE Select ENSP00000221232.5:p.Asn276GlnfsTer?
NM_014516.3:c.821_825dup NP_055331.1:p.Asn276GlnfsTer?
ENST00000221232.9:c.821_825dup ENSP00000221232.5:p.Asn276GlnfsTer?
ENST00000358389.7:c.821_825dup ENSP00000351159.4:p.Asn276GlnfsTer?
ENST00000440571.5:c.586_590dup
ENST00000440571.6:c.824_828dup ENSP00000398463.2:p.Asn277GlnfsTer?
ENST00000447684.5:c.278_282dup ENSP00000411587.2:p.Asn95GlnfsTer?
ENST00000613073.4:c.632_636dup
ENST00000617930.2:c.821_825dup ENSP00000496602.1:p.Asn276GlnfsTer?
ENST00000618939.4:n.1334_1338dup
ENST00000618939.5:n.1359_1363dup
XM_005278279.1:c.824_828dup XP_005278336.1:p.Asn277GlnfsTer?
XM_005278279.2:c.824_828dup XP_005278336.1:p.Asn277GlnfsTer?
XM_005278280.2:c.824_828dup XP_005278337.1:p.Asn277GlnfsTer?
XM_005278281.1:c.821_825dup XP_005278338.1:p.Asn276GlnfsTer?
XM_005278281.2:c.821_825dup XP_005278338.1:p.Asn276GlnfsTer?
XM_005278282.1:c.824_828dup XP_005278339.1:p.Asn277GlnfsTer?
XM_005278282.3:c.824_828dup XP_005278339.1:p.Asn277GlnfsTer?
XM_011526992.1:c.824_828dup XP_011525294.1:p.Asn277GlnfsTer?
XM_011526992.2:c.824_828dup XP_011525294.1:p.Asn277GlnfsTer?
XM_011526993.1:c.824_828dup XP_011525295.1:p.Asn277GlnfsTer?
XM_011526993.3:c.824_828dup XP_011525295.1:p.Asn277GlnfsTer?
XR_002958318.1:n.1119_1123dup
XR_002958319.1:n.1106_1110dup
XR_254515.1:n.1145_1149dup
XR_254515.3:n.1116_1120dup
XR_254516.3:n.1145_1149dup