Canonical Allele Identifier: CA1813521227

Gene: RAD21 UTP23

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116847607_116847608delinsAC , CM000670.2:g.116847607_116847608delinsAC	GRCh38
NC_000008.10:g.117859846_117859847delinsAC , CM000670.1:g.117859846_117859847delinsAC	GRCh37
NC_000008.9:g.117929027_117929028delinsAC	NCBI36
NG_032862.1:g.32259_32260delinsGT , LRG_772:g.32259_32260delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517485.6:c.1788_1789delinsGT (RAD21)	ENSP00000427923.2:p.Lys596=
ENST00000517749.2:c.1788_1789delinsGT (RAD21)	ENSP00000430273.2:p.Lys596=
ENST00000519837.6:c.1788_1789delinsGT (RAD21)	ENSP00000430524.2:p.Lys596=
ENST00000520992.6:c.1788_1789delinsGT (RAD21)	ENSP00000429342.2:p.Lys596=
ENST00000522699.2:c.1788_1789delinsGT (RAD21)	ENSP00000428158.2:p.Lys596=
ENST00000523986.6:n.4757_4758delinsGT (RAD21)
ENST00000685972.1:n.5091_5092delinsGT (RAD21)
ENST00000687122.1:n.4616_4617delinsGT (RAD21)
ENST00000687358.1:c.1788_1789delinsGT (RAD21)	ENSP00000509687.1:p.Lys596=
ENST00000687902.1:c.*163_*164delinsGT (RAD21)	ENSP00000510729.1:n.*163_*164delinsGT
ENST00000689124.1:n.2002_2003delinsGT (RAD21)
ENST00000689154.1:n.1680_1681delinsGT (RAD21)
ENST00000690166.1:n.6657_6658delinsGT (RAD21)
ENST00000297338.7:c.1788_1789delinsGT (RAD21) MANE Select	ENSP00000297338.2:p.Lys596=
ENST00000297338.6:c.1788_1789delinsGT (RAD21)	ENSP00000297338.2:p.Lys596=
ENST00000517749.1:c.102_103delinsGT (RAD21)	ENSP00000430273.1:p.Lys34=
ENST00000517820.1:c.189-1281_189-1280delinsAC (UTP23)	ENSP00000427767.1:n.189-1281_189-1280delinsAC
ENST00000518055.1:c.423_424delinsGT (RAD21)	ENSP00000428003.1:p.Lys141=
ENST00000520733.5:c.46-1281_46-1280delinsAC (UTP23)	ENSP00000429384.1:n.46-1281_46-1280delinsAC
ENST00000521703.5:c.*93-1281_*93-1280delinsAC (UTP23)	ENSP00000428455.1:n.*93-1281_*93-1280delinsAC
ENST00000523986.5:c.300_301delinsGT (RAD21)	ENSP00000428513.1:p.Lys100=
ENST00000524128.1:c.*93-1281_*93-1280delinsAC (UTP23)	ENSP00000430309.1:n.*93-1281_*93-1280delinsAC
NM_006265.2:c.1788_1789delinsGT , LRG_772t1:c.1788_1789delinsGT (RAD21)	NP_006256.1:p.Lys596=
XR_928356.1:n.663-1281_663-1280delinsAC (UTP23)
NM_006265.3:c.1788_1789delinsGT (RAD21) MANE Select	NP_006256.1:p.Lys596=