Canonical Allele Identifier: CA1813520884

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.116847425T= , CM000670.2:g.116847425T= GRCh38
NC_000008.10:g.117859664T= , CM000670.1:g.117859664T= GRCh37
NC_000008.9:g.117928845T= NCBI36
NG_032862.1:g.32442A= , LRG_772:g.32442A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000517485.6:c.*75A= (RAD21) ENSP00000427923.2:n.*75A=
ENST00000517749.2:c.*75A= (RAD21) ENSP00000430273.2:n.*75A=
ENST00000519837.6:c.*75A= (RAD21) ENSP00000430524.2:n.*75A=
ENST00000520992.6:c.*75A= (RAD21) ENSP00000429342.2:n.*75A=
ENST00000522699.2:c.*75A= (RAD21) ENSP00000428158.2:n.*75A=
ENST00000523986.6:n.4940A= (RAD21)
ENST00000685972.1:n.5274A= (RAD21)
ENST00000687122.1:n.4799A= (RAD21)
ENST00000687358.1:c.*75A= (RAD21) ENSP00000509687.1:n.*75A=
ENST00000687902.1:c.*346A= (RAD21) ENSP00000510729.1:n.*346A=
ENST00000689124.1:n.2185A= (RAD21)
ENST00000689154.1:n.1863A= (RAD21)
ENST00000690166.1:n.6840A= (RAD21)
ENST00000297338.7:c.*75A= (RAD21) MANE Select ENSP00000297338.2:n.*75A=
ENST00000297338.6:c.*75A= (RAD21) ENSP00000297338.2:n.*75A=
ENST00000517749.1:c.*75A= (RAD21) ENSP00000430273.1:n.*75A=
ENST00000517820.1:c.189-1463T= (UTP23) ENSP00000427767.1:n.189-1463T=
ENST00000518055.1:c.*75A= (RAD21) ENSP00000428003.1:n.*75A=
ENST00000520733.5:c.46-1463T= (UTP23) ENSP00000429384.1:n.46-1463T=
ENST00000521703.5:c.*93-1463T= (UTP23) ENSP00000428455.1:n.*93-1463T=
ENST00000523986.5:c.*75A= (RAD21) ENSP00000428513.1:n.*75A=
ENST00000524128.1:c.*93-1463T= (UTP23) ENSP00000430309.1:n.*93-1463T=
NM_006265.2:c.*75A= , LRG_772t1:c.*75A= (RAD21) NP_006256.1:n.*75A=
XR_928356.1:n.663-1463T= (UTP23)
NM_006265.3:c.*75A= (RAD21) MANE Select NP_006256.1:n.*75A=