Canonical Allele Identifier: CA846126689

Linked Data

dbSNP Id: rs1316433591

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.116847168_116847170del , CM000670.2:g.116847168_116847170del GRCh38
NC_000008.10:g.117859407_117859409del , CM000670.1:g.117859407_117859409del GRCh37
NC_000008.9:g.117928588_117928590del NCBI36
NG_032862.1:g.32700_32702del , LRG_772:g.32700_32702del

Transcript Alleles

HGVS Amino-acid Change
ENST00000517485.6:c.*333_*335del (RAD21) ENSP00000427923.2:n.*333_*335del
ENST00000517749.2:c.*333_*335del (RAD21) ENSP00000430273.2:n.*333_*335del
ENST00000519837.6:c.*333_*335del (RAD21) ENSP00000430524.2:n.*333_*335del
ENST00000520992.6:c.*333_*335del (RAD21) ENSP00000429342.2:n.*333_*335del
ENST00000522699.2:c.*333_*335del (RAD21) ENSP00000428158.2:n.*333_*335del
ENST00000523986.6:n.5198_5200del (RAD21)
ENST00000685972.1:n.5532_5534del (RAD21)
ENST00000687122.1:n.5057_5059del (RAD21)
ENST00000687358.1:c.*333_*335del (RAD21) ENSP00000509687.1:n.*333_*335del
ENST00000687902.1:c.*604_*606del (RAD21) ENSP00000510729.1:n.*604_*606del
ENST00000689124.1:n.2443_2445del (RAD21)
ENST00000689154.1:n.2121_2123del (RAD21)
ENST00000690166.1:n.7098_7100del (RAD21)
ENST00000297338.7:c.*333_*335del (RAD21) MANE Select ENSP00000297338.2:n.*333_*335del
ENST00000297338.6:c.*333_*335del (RAD21) ENSP00000297338.2:n.*333_*335del
ENST00000517820.1:c.189-1720_189-1718del (UTP23) ENSP00000427767.1:n.189-1720_189-1718del
ENST00000520733.5:c.46-1720_46-1718del (UTP23) ENSP00000429384.1:n.46-1720_46-1718del
ENST00000521703.5:c.*93-1720_*93-1718del (UTP23) ENSP00000428455.1:n.*93-1720_*93-1718del
ENST00000523986.5:c.*333_*335del (RAD21) ENSP00000428513.1:n.*333_*335del
ENST00000524128.1:c.*93-1720_*93-1718del (UTP23) ENSP00000430309.1:n.*93-1720_*93-1718del
NM_006265.2:c.*333_*335del , LRG_772t1:c.*333_*335del (RAD21) NP_006256.1:n.*333_*335del
XR_928356.1:n.663-1720_663-1718del (UTP23)
NM_006265.3:c.*333_*335del (RAD21) MANE Select NP_006256.1:n.*333_*335del