Canonical Allele Identifier: CA1813520702

Gene: RAD21 UTP23

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116847281G= , CM000670.2:g.116847281G=	GRCh38
NC_000008.10:g.117859520G= , CM000670.1:g.117859520G=	GRCh37
NC_000008.9:g.117928701G=	NCBI36
NG_032862.1:g.32586C= , LRG_772:g.32586C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517485.6:c.*219C= (RAD21)	ENSP00000427923.2:n.*219C=
ENST00000517749.2:c.*219C= (RAD21)	ENSP00000430273.2:n.*219C=
ENST00000519837.6:c.*219C= (RAD21)	ENSP00000430524.2:n.*219C=
ENST00000520992.6:c.*219C= (RAD21)	ENSP00000429342.2:n.*219C=
ENST00000522699.2:c.*219C= (RAD21)	ENSP00000428158.2:n.*219C=
ENST00000523986.6:n.5084C= (RAD21)
ENST00000685972.1:n.5418C= (RAD21)
ENST00000687122.1:n.4943C= (RAD21)
ENST00000687358.1:c.*219C= (RAD21)	ENSP00000509687.1:n.*219C=
ENST00000687902.1:c.*490C= (RAD21)	ENSP00000510729.1:n.*490C=
ENST00000689124.1:n.2329C= (RAD21)
ENST00000689154.1:n.2007C= (RAD21)
ENST00000690166.1:n.6984C= (RAD21)
ENST00000297338.7:c.*219C= (RAD21) MANE Select	ENSP00000297338.2:n.*219C=
ENST00000297338.6:c.*219C= (RAD21)	ENSP00000297338.2:n.*219C=
ENST00000517749.1:c.*219C= (RAD21)	ENSP00000430273.1:n.*219C=
ENST00000517820.1:c.189-1607G= (UTP23)	ENSP00000427767.1:n.189-1607G=
ENST00000520733.5:c.46-1607G= (UTP23)	ENSP00000429384.1:n.46-1607G=
ENST00000521703.5:c.*93-1607G= (UTP23)	ENSP00000428455.1:n.*93-1607G=
ENST00000523986.5:c.*219C= (RAD21)	ENSP00000428513.1:n.*219C=
ENST00000524128.1:c.*93-1607G= (UTP23)	ENSP00000430309.1:n.*93-1607G=
NM_006265.2:c.*219C= , LRG_772t1:c.*219C= (RAD21)	NP_006256.1:n.*219C=
XR_928356.1:n.663-1607G= (UTP23)
NM_006265.3:c.*219C= (RAD21) MANE Select	NP_006256.1:n.*219C=