Canonical Allele Identifier: CA1813521375

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.116847676T= , CM000670.2:g.116847676T= GRCh38
NC_000008.10:g.117859915T= , CM000670.1:g.117859915T= GRCh37
NC_000008.9:g.117929096T= NCBI36
NG_032862.1:g.32191A= , LRG_772:g.32191A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000517485.6:c.1720A= (RAD21) ENSP00000427923.2:p.Thr574=
ENST00000517749.2:c.1720A= (RAD21) ENSP00000430273.2:p.Thr574=
ENST00000519837.6:c.1720A= (RAD21) ENSP00000430524.2:p.Thr574=
ENST00000520992.6:c.1720A= (RAD21) ENSP00000429342.2:p.Thr574=
ENST00000522699.2:c.1720A= (RAD21) ENSP00000428158.2:p.Thr574=
ENST00000523986.6:n.4689A= (RAD21)
ENST00000685972.1:n.5023A= (RAD21)
ENST00000687122.1:n.4548A= (RAD21)
ENST00000687358.1:c.1720A= (RAD21) ENSP00000509687.1:p.Thr574=
ENST00000687902.1:c.*95A= (RAD21) ENSP00000510729.1:n.*95A=
ENST00000689124.1:n.1934A= (RAD21)
ENST00000689154.1:n.1612A= (RAD21)
ENST00000690166.1:n.6589A= (RAD21)
ENST00000297338.7:c.1720A= (RAD21) MANE Select ENSP00000297338.2:p.Thr574=
ENST00000297338.6:c.1720A= (RAD21) ENSP00000297338.2:p.Thr574=
ENST00000517749.1:c.34A= (RAD21) ENSP00000430273.1:p.Thr12=
ENST00000517820.1:c.189-1212T= (UTP23) ENSP00000427767.1:n.189-1212T=
ENST00000518055.1:c.355A= (RAD21) ENSP00000428003.1:p.Thr119=
ENST00000520733.5:c.46-1212T= (UTP23) ENSP00000429384.1:n.46-1212T=
ENST00000521703.5:c.*93-1212T= (UTP23) ENSP00000428455.1:n.*93-1212T=
ENST00000523986.5:c.232A= (RAD21) ENSP00000428513.1:p.Thr78=
ENST00000524128.1:c.*93-1212T= (UTP23) ENSP00000430309.1:n.*93-1212T=
NM_006265.2:c.1720A= , LRG_772t1:c.1720A= (RAD21) NP_006256.1:p.Thr574=
XR_928356.1:n.663-1212T= (UTP23)
NM_006265.3:c.1720A= (RAD21) MANE Select NP_006256.1:p.Thr574=