Canonical Allele Identifier: CA2688331422

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.116847240_116847244del , CM000670.2:g.116847240_116847244del GRCh38
NC_000008.10:g.117859479_117859483del , CM000670.1:g.117859479_117859483del GRCh37
NC_000008.9:g.117928660_117928664del NCBI36
NG_032862.1:g.32627_32631del , LRG_772:g.32627_32631del

Transcript Alleles

HGVS Amino-acid Change
ENST00000517485.6:c.*260_*264del (RAD21) ENSP00000427923.2:n.*260_*264del
ENST00000517749.2:c.*260_*264del (RAD21) ENSP00000430273.2:n.*260_*264del
ENST00000519837.6:c.*260_*264del (RAD21) ENSP00000430524.2:n.*260_*264del
ENST00000520992.6:c.*260_*264del (RAD21) ENSP00000429342.2:n.*260_*264del
ENST00000522699.2:c.*260_*264del (RAD21) ENSP00000428158.2:n.*260_*264del
ENST00000523986.6:n.5125_5129del (RAD21)
ENST00000685972.1:n.5459_5463del (RAD21)
ENST00000687122.1:n.4984_4988del (RAD21)
ENST00000687358.1:c.*260_*264del (RAD21) ENSP00000509687.1:n.*260_*264del
ENST00000687902.1:c.*531_*535del (RAD21) ENSP00000510729.1:n.*531_*535del
ENST00000689124.1:n.2370_2374del (RAD21)
ENST00000689154.1:n.2048_2052del (RAD21)
ENST00000690166.1:n.7025_7029del (RAD21)
ENST00000297338.7:c.*260_*264del (RAD21) MANE Select ENSP00000297338.2:n.*260_*264del
ENST00000297338.6:c.*260_*264del (RAD21) ENSP00000297338.2:n.*260_*264del
ENST00000517749.1:c.*260_*264del (RAD21) ENSP00000430273.1:n.*260_*264del
ENST00000517820.1:c.189-1648_189-1644del (UTP23) ENSP00000427767.1:n.189-1648_189-1644del
ENST00000520733.5:c.46-1648_46-1644del (UTP23) ENSP00000429384.1:n.46-1648_46-1644del
ENST00000521703.5:c.*93-1648_*93-1644del (UTP23) ENSP00000428455.1:n.*93-1648_*93-1644del
ENST00000523986.5:c.*260_*264del (RAD21) ENSP00000428513.1:n.*260_*264del
ENST00000524128.1:c.*93-1648_*93-1644del (UTP23) ENSP00000430309.1:n.*93-1648_*93-1644del
NM_006265.2:c.*260_*264del , LRG_772t1:c.*260_*264del (RAD21) NP_006256.1:n.*260_*264del
XR_928356.1:n.663-1648_663-1644del (UTP23)
NM_006265.3:c.*260_*264del (RAD21) MANE Select NP_006256.1:n.*260_*264del