Canonical Allele Identifier: CA2603865447

Gene: RAD21 UTP23

Linked Data

• gnomAD v3: 8-116847189-CTT-C
• gnomAD v4: 8-116847189-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116847192_116847193del , CM000670.2:g.116847192_116847193del	GRCh38
NC_000008.10:g.117859431_117859432del , CM000670.1:g.117859431_117859432del	GRCh37
NC_000008.9:g.117928612_117928613del	NCBI36
NG_032862.1:g.32676_32677del , LRG_772:g.32676_32677del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517485.6:c.*309_*310del (RAD21)	ENSP00000427923.2:n.*309_*310del
ENST00000517749.2:c.*309_*310del (RAD21)	ENSP00000430273.2:n.*309_*310del
ENST00000519837.6:c.*309_*310del (RAD21)	ENSP00000430524.2:n.*309_*310del
ENST00000520992.6:c.*309_*310del (RAD21)	ENSP00000429342.2:n.*309_*310del
ENST00000522699.2:c.*309_*310del (RAD21)	ENSP00000428158.2:n.*309_*310del
ENST00000523986.6:n.5174_5175del (RAD21)
ENST00000685972.1:n.5508_5509del (RAD21)
ENST00000687122.1:n.5033_5034del (RAD21)
ENST00000687358.1:c.*309_*310del (RAD21)	ENSP00000509687.1:n.*309_*310del
ENST00000687902.1:c.*580_*581del (RAD21)	ENSP00000510729.1:n.*580_*581del
ENST00000689124.1:n.2419_2420del (RAD21)
ENST00000689154.1:n.2097_2098del (RAD21)
ENST00000690166.1:n.7074_7075del (RAD21)
ENST00000297338.7:c.*309_*310del (RAD21) MANE Select	ENSP00000297338.2:n.*309_*310del
ENST00000297338.6:c.*309_*310del (RAD21)	ENSP00000297338.2:n.*309_*310del
ENST00000517820.1:c.189-1696_189-1695del (UTP23)	ENSP00000427767.1:n.189-1696_189-1695del
ENST00000520733.5:c.46-1696_46-1695del (UTP23)	ENSP00000429384.1:n.46-1696_46-1695del
ENST00000521703.5:c.*93-1696_*93-1695del (UTP23)	ENSP00000428455.1:n.*93-1696_*93-1695del
ENST00000523986.5:c.*309_*310del (RAD21)	ENSP00000428513.1:n.*309_*310del
ENST00000524128.1:c.*93-1696_*93-1695del (UTP23)	ENSP00000430309.1:n.*93-1696_*93-1695del
NM_006265.2:c.*309_*310del , LRG_772t1:c.*309_*310del (RAD21)	NP_006256.1:n.*309_*310del
XR_928356.1:n.663-1696_663-1695del (UTP23)
NM_006265.3:c.*309_*310del (RAD21) MANE Select	NP_006256.1:n.*309_*310del