Canonical Allele Identifier: CA1118284361

Linked Data

dbSNP Id: rs1812273482

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.116847642_116847700dup , CM000670.2:g.116847642_116847700dup GRCh38
NC_000008.10:g.117859881_117859939dup , CM000670.1:g.117859881_117859939dup GRCh37
NC_000008.9:g.117929062_117929120dup NCBI36
NG_032862.1:g.32168_32226dup , LRG_772:g.32168_32226dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000517485.6:c.1705-8_1755dup (RAD21)
ENST00000517749.2:c.1705-8_1755dup (RAD21)
ENST00000519837.6:c.1705-8_1755dup (RAD21)
ENST00000520992.6:c.1705-8_1755dup (RAD21)
ENST00000522699.2:c.1705-8_1755dup (RAD21)
ENST00000523986.6:n.4674-8_4724dup (RAD21)
ENST00000685972.1:n.5008-8_5058dup (RAD21)
ENST00000687122.1:n.4533-8_4583dup (RAD21)
ENST00000687358.1:c.1705-8_1755dup (RAD21)
ENST00000687902.1:c.*80-8_*130dup (RAD21)
ENST00000689124.1:n.1919-8_1969dup (RAD21)
ENST00000689154.1:n.1589_1647dup (RAD21)
ENST00000690166.1:n.6566_6624dup (RAD21)
ENST00000297338.7:c.1705-8_1755dup (RAD21)
ENST00000297338.6:c.1705-8_1755dup (RAD21)
ENST00000517749.1:c.19-8_69dup (RAD21)
ENST00000517820.1:c.189-1246_189-1188dup (UTP23) ENSP00000427767.1:n.189-1246_189-1188dup
ENST00000518055.1:c.340-8_390dup (RAD21)
ENST00000520733.5:c.46-1246_46-1188dup (UTP23) ENSP00000429384.1:n.46-1246_46-1188dup
ENST00000521703.5:c.*93-1246_*93-1188dup (UTP23) ENSP00000428455.1:n.*93-1246_*93-1188dup
ENST00000523986.5:c.217-8_267dup (RAD21)
ENST00000524128.1:c.*93-1246_*93-1188dup (UTP23) ENSP00000430309.1:n.*93-1246_*93-1188dup
NM_006265.2:c.1705-8_1755dup , LRG_772t1:c.1705-8_1755dup (RAD21)
XR_928356.1:n.663-1246_663-1188dup (UTP23)
NM_006265.3:c.1705-8_1755dup (RAD21)