Canonical Allele Identifier: CA371992622

Gene: RAD21 UTP23

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116848956T>C , CM000670.2:g.116848956T>C	GRCh38
NC_000008.10:g.117861195T>C , CM000670.1:g.117861195T>C	GRCh37
NC_000008.9:g.117930376T>C	NCBI36
NG_032862.1:g.30911A>G , LRG_772:g.30911A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006265.3:c.1694A>G (RAD21) MANE Select	NP_006256.1:p.His565Arg
ENST00000297338.7:c.1694A>G (RAD21) MANE Select	ENSP00000297338.2:p.His565Arg
NM_006265.2:c.1694A>G , LRG_772t1:c.1694A>G (RAD21)	NP_006256.1:p.His565Arg
ENST00000297338.6:c.1694A>G (RAD21)	ENSP00000297338.2:p.His565Arg
ENST00000517485.6:c.1694A>G (RAD21)	ENSP00000427923.2:p.His565Arg
ENST00000517749.1:c.8A>G (RAD21)	ENSP00000430273.1:p.His3Arg
ENST00000517749.2:c.1694A>G (RAD21)	ENSP00000430273.2:p.His565Arg
ENST00000517820.1:c.257T>C (UTP23)	ENSP00000427767.1:p.Met86Thr
ENST00000518055.1:c.329A>G (RAD21)	ENSP00000428003.1:p.His110Arg
ENST00000519837.6:c.1694A>G (RAD21)	ENSP00000430524.2:p.His565Arg
ENST00000520733.5:c.114T>C (UTP23)	ENSP00000429384.1:p.His38=
ENST00000520992.6:c.1694A>G (RAD21)	ENSP00000429342.2:p.His565Arg
ENST00000521703.5:c.*161T>C (UTP23)	ENSP00000428455.1:n.*161T>C
ENST00000522699.2:c.1694A>G (RAD21)	ENSP00000428158.2:p.His565Arg
ENST00000523547.2:n.1804A>G (RAD21)
ENST00000523986.5:c.206A>G (RAD21)	ENSP00000428513.1:p.His69Arg
ENST00000523986.6:n.4663A>G (RAD21)
ENST00000524128.1:c.*161T>C (UTP23)	ENSP00000430309.1:n.*161T>C
ENST00000685972.1:n.4997A>G (RAD21)
ENST00000686622.1:n.5054A>G (RAD21)
ENST00000687122.1:n.4522A>G (RAD21)
ENST00000687358.1:c.1694A>G (RAD21)	ENSP00000509687.1:p.His565Arg
ENST00000687902.1:c.*69A>G (RAD21)	ENSP00000510729.1:n.*69A>G
ENST00000688033.1:n.6520A>G (RAD21)
ENST00000689124.1:n.1908A>G (RAD21)
ENST00000689154.1:n.332A>G (RAD21)
ENST00000690166.1:n.5309A>G (RAD21)
ENST00000690189.1:n.8265A>G (RAD21)
XR_928356.1:n.731T>C (UTP23)