Canonical Allele Identifier: CA2695210070

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.116847673_116847674del , CM000670.2:g.116847673_116847674del GRCh38
NC_000008.10:g.117859912_117859913del , CM000670.1:g.117859912_117859913del GRCh37
NC_000008.9:g.117929093_117929094del NCBI36
NG_032862.1:g.32193_32194del , LRG_772:g.32193_32194del

Transcript Alleles

HGVS Amino-acid Change
ENST00000517485.6:c.1722_1723del (RAD21) ENSP00000427923.2:p.Gly575SerfsTer2
ENST00000517749.2:c.1722_1723del (RAD21) ENSP00000430273.2:p.Gly575SerfsTer2
ENST00000519837.6:c.1722_1723del (RAD21) ENSP00000430524.2:p.Gly575SerfsTer2
ENST00000520992.6:c.1722_1723del (RAD21) ENSP00000429342.2:p.Gly575SerfsTer2
ENST00000522699.2:c.1722_1723del (RAD21) ENSP00000428158.2:p.Gly575SerfsTer2
ENST00000523986.6:n.4691_4692del (RAD21)
ENST00000685972.1:n.5025_5026del (RAD21)
ENST00000687122.1:n.4550_4551del (RAD21)
ENST00000687358.1:c.1722_1723del (RAD21) ENSP00000509687.1:p.Gly575SerfsTer2
ENST00000687902.1:c.*97_*98del (RAD21) ENSP00000510729.1:n.*97_*98del
ENST00000689124.1:n.1936_1937del (RAD21)
ENST00000689154.1:n.1614_1615del (RAD21)
ENST00000690166.1:n.6591_6592del (RAD21)
ENST00000297338.7:c.1722_1723del (RAD21) MANE Select ENSP00000297338.2:p.Gly575SerfsTer2
ENST00000297338.6:c.1722_1723del (RAD21) ENSP00000297338.2:p.Gly575SerfsTer2
ENST00000517749.1:c.36_37del (RAD21) ENSP00000430273.1:p.Gly13SerfsTer2
ENST00000517820.1:c.189-1215_189-1214del (UTP23) ENSP00000427767.1:n.189-1215_189-1214del
ENST00000518055.1:c.357_358del (RAD21) ENSP00000428003.1:p.Gly120SerfsTer2
ENST00000520733.5:c.46-1215_46-1214del (UTP23) ENSP00000429384.1:n.46-1215_46-1214del
ENST00000521703.5:c.*93-1215_*93-1214del (UTP23) ENSP00000428455.1:n.*93-1215_*93-1214del
ENST00000523986.5:c.234_235del (RAD21) ENSP00000428513.1:p.Gly79SerfsTer2
ENST00000524128.1:c.*93-1215_*93-1214del (UTP23) ENSP00000430309.1:n.*93-1215_*93-1214del
NM_006265.2:c.1722_1723del , LRG_772t1:c.1722_1723del (RAD21) NP_006256.1:p.Gly575SerfsTer2
XR_928356.1:n.663-1215_663-1214del (UTP23)
NM_006265.3:c.1722_1723del (RAD21) MANE Select NP_006256.1:p.Gly575SerfsTer2