Canonical Allele Identifier: CA652821131

Gene: RAD21 UTP23

Linked Data

• COSMIC: COSN16869483

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116847498_116847499insG , CM000670.2:g.116847498_116847499insG	GRCh38
NC_000008.10:g.117859737_117859738insG , CM000670.1:g.117859737_117859738insG	GRCh37
NC_000008.9:g.117928918_117928919insG	NCBI36
NG_032862.1:g.32368_32369insC , LRG_772:g.32368_32369insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517485.6:c.*1_*2insC (RAD21)	ENSP00000427923.2:n.*1_*2insC
ENST00000517749.2:c.*1_*2insC (RAD21)	ENSP00000430273.2:n.*1_*2insC
ENST00000519837.6:c.*1_*2insC (RAD21)	ENSP00000430524.2:n.*1_*2insC
ENST00000520992.6:c.*1_*2insC (RAD21)	ENSP00000429342.2:n.*1_*2insC
ENST00000522699.2:c.*1_*2insC (RAD21)	ENSP00000428158.2:n.*1_*2insC
ENST00000523986.6:n.4866_4867insC (RAD21)
ENST00000685972.1:n.5200_5201insC (RAD21)
ENST00000687122.1:n.4725_4726insC (RAD21)
ENST00000687358.1:c.*1_*2insC (RAD21)	ENSP00000509687.1:n.*1_*2insC
ENST00000687902.1:c.*272_*273insC (RAD21)	ENSP00000510729.1:n.*272_*273insC
ENST00000689124.1:n.2111_2112insC (RAD21)
ENST00000689154.1:n.1789_1790insC (RAD21)
ENST00000690166.1:n.6766_6767insC (RAD21)
ENST00000297338.7:c.*1_*2insC (RAD21) MANE Select	ENSP00000297338.2:n.*1_*2insC
ENST00000297338.6:c.*1_*2insC (RAD21)	ENSP00000297338.2:n.*1_*2insC
ENST00000517749.1:c.*1_*2insC (RAD21)	ENSP00000430273.1:n.*1_*2insC
ENST00000517820.1:c.189-1390_189-1389insG (UTP23)	ENSP00000427767.1:n.189-1390_189-1389insG
ENST00000518055.1:c.*1_*2insC (RAD21)	ENSP00000428003.1:n.*1_*2insC
ENST00000520733.5:c.46-1390_46-1389insG (UTP23)	ENSP00000429384.1:n.46-1390_46-1389insG
ENST00000521703.5:c.*93-1390_*93-1389insG (UTP23)	ENSP00000428455.1:n.*93-1390_*93-1389insG
ENST00000523986.5:c.*1_*2insC (RAD21)	ENSP00000428513.1:n.*1_*2insC
ENST00000524128.1:c.*93-1390_*93-1389insG (UTP23)	ENSP00000430309.1:n.*93-1390_*93-1389insG
NM_006265.2:c.*1_*2insC , LRG_772t1:c.*1_*2insC (RAD21)	NP_006256.1:n.*1_*2insC
XR_928356.1:n.663-1390_663-1389insG (UTP23)
NM_006265.3:c.*1_*2insC (RAD21) MANE Select	NP_006256.1:n.*1_*2insC