Canonical Allele Identifier: CA1813521267

Gene: RAD21 UTP23

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116847626T= , CM000670.2:g.116847626T=	GRCh38
NC_000008.10:g.117859865T= , CM000670.1:g.117859865T=	GRCh37
NC_000008.9:g.117929046T=	NCBI36
NG_032862.1:g.32241A= , LRG_772:g.32241A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517485.6:c.1770A= (RAD21)	ENSP00000427923.2:p.Arg590=
ENST00000517749.2:c.1770A= (RAD21)	ENSP00000430273.2:p.Arg590=
ENST00000519837.6:c.1770A= (RAD21)	ENSP00000430524.2:p.Arg590=
ENST00000520992.6:c.1770A= (RAD21)	ENSP00000429342.2:p.Arg590=
ENST00000522699.2:c.1770A= (RAD21)	ENSP00000428158.2:p.Arg590=
ENST00000523986.6:n.4739A= (RAD21)
ENST00000685972.1:n.5073A= (RAD21)
ENST00000687122.1:n.4598A= (RAD21)
ENST00000687358.1:c.1770A= (RAD21)	ENSP00000509687.1:p.Arg590=
ENST00000687902.1:c.*145A= (RAD21)	ENSP00000510729.1:n.*145A=
ENST00000689124.1:n.1984A= (RAD21)
ENST00000689154.1:n.1662A= (RAD21)
ENST00000690166.1:n.6639A= (RAD21)
ENST00000297338.7:c.1770A= (RAD21) MANE Select	ENSP00000297338.2:p.Arg590=
ENST00000297338.6:c.1770A= (RAD21)	ENSP00000297338.2:p.Arg590=
ENST00000517749.1:c.84A= (RAD21)	ENSP00000430273.1:p.Arg28=
ENST00000517820.1:c.189-1262T= (UTP23)	ENSP00000427767.1:n.189-1262T=
ENST00000518055.1:c.405A= (RAD21)	ENSP00000428003.1:p.Arg135=
ENST00000520733.5:c.46-1262T= (UTP23)	ENSP00000429384.1:n.46-1262T=
ENST00000521703.5:c.*93-1262T= (UTP23)	ENSP00000428455.1:n.*93-1262T=
ENST00000523986.5:c.282A= (RAD21)	ENSP00000428513.1:p.Arg94=
ENST00000524128.1:c.*93-1262T= (UTP23)	ENSP00000430309.1:n.*93-1262T=
NM_006265.2:c.1770A= , LRG_772t1:c.1770A= (RAD21)	NP_006256.1:p.Arg590=
XR_928356.1:n.663-1262T= (UTP23)
NM_006265.3:c.1770A= (RAD21) MANE Select	NP_006256.1:p.Arg590=