Canonical Allele Identifier: CA1813520507

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.116847164_116847167delinsTGAA , CM000670.2:g.116847164_116847167delinsTGAA GRCh38
NC_000008.10:g.117859403_117859406delinsTGAA , CM000670.1:g.117859403_117859406delinsTGAA GRCh37
NC_000008.9:g.117928584_117928587delinsTGAA NCBI36
NG_032862.1:g.32700_32703delinsTTCA , LRG_772:g.32700_32703delinsTTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000517485.6:c.*333_*336delinsTTCA (RAD21) ENSP00000427923.2:n.*333_*336delinsTTCA
ENST00000517749.2:c.*333_*336delinsTTCA (RAD21) ENSP00000430273.2:n.*333_*336delinsTTCA
ENST00000519837.6:c.*333_*336delinsTTCA (RAD21) ENSP00000430524.2:n.*333_*336delinsTTCA
ENST00000520992.6:c.*333_*336delinsTTCA (RAD21) ENSP00000429342.2:n.*333_*336delinsTTCA
ENST00000522699.2:c.*333_*336delinsTTCA (RAD21) ENSP00000428158.2:n.*333_*336delinsTTCA
ENST00000523986.6:n.5198_5201delinsTTCA (RAD21)
ENST00000685972.1:n.5532_5535delinsTTCA (RAD21)
ENST00000687122.1:n.5057_5060delinsTTCA (RAD21)
ENST00000687358.1:c.*333_*336delinsTTCA (RAD21) ENSP00000509687.1:n.*333_*336delinsTTCA
ENST00000687902.1:c.*604_*607delinsTTCA (RAD21) ENSP00000510729.1:n.*604_*607delinsTTCA
ENST00000689124.1:n.2443_2446delinsTTCA (RAD21)
ENST00000689154.1:n.2121_2124delinsTTCA (RAD21)
ENST00000690166.1:n.7098_7101delinsTTCA (RAD21)
ENST00000297338.7:c.*333_*336delinsTTCA (RAD21) MANE Select ENSP00000297338.2:n.*333_*336delinsTTCA
ENST00000297338.6:c.*333_*336delinsTTCA (RAD21) ENSP00000297338.2:n.*333_*336delinsTTCA
ENST00000517820.1:c.189-1724_189-1721delinsTGAA (UTP23) ENSP00000427767.1:n.189-1724_189-1721delinsTGAA
ENST00000520733.5:c.46-1724_46-1721delinsTGAA (UTP23) ENSP00000429384.1:n.46-1724_46-1721delinsTGAA
ENST00000521703.5:c.*93-1724_*93-1721delinsTGAA (UTP23) ENSP00000428455.1:n.*93-1724_*93-1721delinsTGAA
ENST00000523986.5:c.*333_*336delinsTTCA (RAD21) ENSP00000428513.1:n.*333_*336delinsTTCA
ENST00000524128.1:c.*93-1724_*93-1721delinsTGAA (UTP23) ENSP00000430309.1:n.*93-1724_*93-1721delinsTGAA
NM_006265.2:c.*333_*336delinsTTCA , LRG_772t1:c.*333_*336delinsTTCA (RAD21) NP_006256.1:n.*333_*336delinsTTCA
XR_928356.1:n.663-1724_663-1721delinsTGAA (UTP23)
NM_006265.3:c.*333_*336delinsTTCA (RAD21) MANE Select NP_006256.1:n.*333_*336delinsTTCA