Canonical Allele Identifier: CA1813521378

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.116847677T= , CM000670.2:g.116847677T= GRCh38
NC_000008.10:g.117859916T= , CM000670.1:g.117859916T= GRCh37
NC_000008.9:g.117929097T= NCBI36
NG_032862.1:g.32190A= , LRG_772:g.32190A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000517485.6:c.1719A= (RAD21) ENSP00000427923.2:p.Lys573=
ENST00000517749.2:c.1719A= (RAD21) ENSP00000430273.2:p.Lys573=
ENST00000519837.6:c.1719A= (RAD21) ENSP00000430524.2:p.Lys573=
ENST00000520992.6:c.1719A= (RAD21) ENSP00000429342.2:p.Lys573=
ENST00000522699.2:c.1719A= (RAD21) ENSP00000428158.2:p.Lys573=
ENST00000523986.6:n.4688A= (RAD21)
ENST00000685972.1:n.5022A= (RAD21)
ENST00000687122.1:n.4547A= (RAD21)
ENST00000687358.1:c.1719A= (RAD21) ENSP00000509687.1:p.Lys573=
ENST00000687902.1:c.*94A= (RAD21) ENSP00000510729.1:n.*94A=
ENST00000689124.1:n.1933A= (RAD21)
ENST00000689154.1:n.1611A= (RAD21)
ENST00000690166.1:n.6588A= (RAD21)
ENST00000297338.7:c.1719A= (RAD21) MANE Select ENSP00000297338.2:p.Lys573=
ENST00000297338.6:c.1719A= (RAD21) ENSP00000297338.2:p.Lys573=
ENST00000517749.1:c.33A= (RAD21) ENSP00000430273.1:p.Lys11=
ENST00000517820.1:c.189-1211T= (UTP23) ENSP00000427767.1:n.189-1211T=
ENST00000518055.1:c.354A= (RAD21) ENSP00000428003.1:p.Lys118=
ENST00000520733.5:c.46-1211T= (UTP23) ENSP00000429384.1:n.46-1211T=
ENST00000521703.5:c.*93-1211T= (UTP23) ENSP00000428455.1:n.*93-1211T=
ENST00000523986.5:c.231A= (RAD21) ENSP00000428513.1:p.Lys77=
ENST00000524128.1:c.*93-1211T= (UTP23) ENSP00000430309.1:n.*93-1211T=
NM_006265.2:c.1719A= , LRG_772t1:c.1719A= (RAD21) NP_006256.1:p.Lys573=
XR_928356.1:n.663-1211T= (UTP23)
NM_006265.3:c.1719A= (RAD21) MANE Select NP_006256.1:p.Lys573=