Canonical Allele Identifier: CA2688331596

Gene: RAD21 UTP23

Linked Data

• gnomAD v4: 8-116847689-ACGCTG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116847690_116847694del , CM000670.2:g.116847690_116847694del	GRCh38
NC_000008.10:g.117859929_117859933del , CM000670.1:g.117859929_117859933del	GRCh37
NC_000008.9:g.117929110_117929114del	NCBI36
NG_032862.1:g.32173_32177del , LRG_772:g.32173_32177del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517485.6:c.1705-3_1706del (RAD21)
ENST00000517749.2:c.1705-3_1706del (RAD21)
ENST00000519837.6:c.1705-3_1706del (RAD21)
ENST00000520992.6:c.1705-3_1706del (RAD21)
ENST00000522699.2:c.1705-3_1706del (RAD21)
ENST00000523986.6:n.4674-3_4675del (RAD21)
ENST00000685972.1:n.5008-3_5009del (RAD21)
ENST00000687122.1:n.4533-3_4534del (RAD21)
ENST00000687358.1:c.1705-3_1706del (RAD21)
ENST00000687902.1:c.*80-3_*81del (RAD21)
ENST00000689124.1:n.1919-3_1920del (RAD21)
ENST00000689154.1:n.1594_1598del (RAD21)
ENST00000690166.1:n.6571_6575del (RAD21)
ENST00000297338.7:c.1705-3_1706del (RAD21)
ENST00000297338.6:c.1705-3_1706del (RAD21)
ENST00000517749.1:c.19-3_20del (RAD21)
ENST00000517820.1:c.189-1198_189-1194del (UTP23)	ENSP00000427767.1:n.189-1198_189-1194del
ENST00000518055.1:c.340-3_341del (RAD21)
ENST00000520733.5:c.46-1198_46-1194del (UTP23)	ENSP00000429384.1:n.46-1198_46-1194del
ENST00000521703.5:c.*93-1198_*93-1194del (UTP23)	ENSP00000428455.1:n.*93-1198_*93-1194del
ENST00000523986.5:c.217-3_218del (RAD21)
ENST00000524128.1:c.*93-1198_*93-1194del (UTP23)	ENSP00000430309.1:n.*93-1198_*93-1194del
NM_006265.2:c.1705-3_1706del , LRG_772t1:c.1705-3_1706del (RAD21)
XR_928356.1:n.663-1198_663-1194del (UTP23)
NM_006265.3:c.1705-3_1706del (RAD21)