Canonical Allele Identifier: CA1813521502

Gene: RAD21 UTP23

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116847760_116847761delinsAC , CM000670.2:g.116847760_116847761delinsAC	GRCh38
NC_000008.10:g.117859999_117860000delinsAC , CM000670.1:g.117859999_117860000delinsAC	GRCh37
NC_000008.9:g.117929180_117929181delinsAC	NCBI36
NG_032862.1:g.32106_32107delinsGT , LRG_772:g.32106_32107delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517485.6:c.1705-70_1705-69delinsGT (RAD21)	ENSP00000427923.2:n.1705-70_1705-69delinsGT
ENST00000517749.2:c.1705-70_1705-69delinsGT (RAD21)	ENSP00000430273.2:n.1705-70_1705-69delinsGT
ENST00000519837.6:c.1705-70_1705-69delinsGT (RAD21)	ENSP00000430524.2:n.1705-70_1705-69delinsGT
ENST00000520992.6:c.1705-70_1705-69delinsGT (RAD21)	ENSP00000429342.2:n.1705-70_1705-69delinsGT
ENST00000522699.2:c.1705-70_1705-69delinsGT (RAD21)	ENSP00000428158.2:n.1705-70_1705-69delinsGT
ENST00000523986.6:n.4674-70_4674-69delinsGT (RAD21)
ENST00000685972.1:n.5008-70_5008-69delinsGT (RAD21)
ENST00000687122.1:n.4533-70_4533-69delinsGT (RAD21)
ENST00000687358.1:c.1705-70_1705-69delinsGT (RAD21)	ENSP00000509687.1:n.1705-70_1705-69delinsGT
ENST00000687902.1:c.*80-70_*80-69delinsGT (RAD21)	ENSP00000510729.1:n.*80-70_*80-69delinsGT
ENST00000689124.1:n.1919-70_1919-69delinsGT (RAD21)
ENST00000689154.1:n.1527_1528delinsGT (RAD21)
ENST00000690166.1:n.6504_6505delinsGT (RAD21)
ENST00000297338.7:c.1705-70_1705-69delinsGT (RAD21) MANE Select	ENSP00000297338.2:n.1705-70_1705-69delinsGT
ENST00000297338.6:c.1705-70_1705-69delinsGT (RAD21)	ENSP00000297338.2:n.1705-70_1705-69delinsGT
ENST00000517749.1:c.19-70_19-69delinsGT (RAD21)	ENSP00000430273.1:n.19-70_19-69delinsGT
ENST00000517820.1:c.189-1128_189-1127delinsAC (UTP23)	ENSP00000427767.1:n.189-1128_189-1127delinsAC
ENST00000518055.1:c.340-70_340-69delinsGT (RAD21)	ENSP00000428003.1:n.340-70_340-69delinsGT
ENST00000520733.5:c.46-1128_46-1127delinsAC (UTP23)	ENSP00000429384.1:n.46-1128_46-1127delinsAC
ENST00000521703.5:c.*93-1128_*93-1127delinsAC (UTP23)	ENSP00000428455.1:n.*93-1128_*93-1127delinsAC
ENST00000523986.5:c.217-70_217-69delinsGT (RAD21)	ENSP00000428513.1:n.217-70_217-69delinsGT
ENST00000524128.1:c.*93-1128_*93-1127delinsAC (UTP23)	ENSP00000430309.1:n.*93-1128_*93-1127delinsAC
NM_006265.2:c.1705-70_1705-69delinsGT , LRG_772t1:c.1705-70_1705-69delinsGT (RAD21)	NP_006256.1:n.1705-70_1705-69delinsGT
XR_928356.1:n.663-1128_663-1127delinsAC (UTP23)
NM_006265.3:c.1705-70_1705-69delinsGT (RAD21) MANE Select	NP_006256.1:n.1705-70_1705-69delinsGT