Canonical Allele Identifier: CA846126824

Gene: RAD21 UTP23

Linked Data

• dbSNP Id: rs1257014441
• gnomAD v4: 8-116847367-TGAA-T
• MyVariant Identifiers: chr8:g.117859607_117859609del (hg19) ; chr8:g.116847368_116847370del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116847372_116847374del , CM000670.2:g.116847372_116847374del	GRCh38
NC_000008.10:g.117859611_117859613del , CM000670.1:g.117859611_117859613del	GRCh37
NC_000008.9:g.117928792_117928794del	NCBI36
NG_032862.1:g.32497_32499del , LRG_772:g.32497_32499del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517485.6:c.*130_*132del (RAD21)	ENSP00000427923.2:n.*130_*132del
ENST00000517749.2:c.*130_*132del (RAD21)	ENSP00000430273.2:n.*130_*132del
ENST00000519837.6:c.*130_*132del (RAD21)	ENSP00000430524.2:n.*130_*132del
ENST00000520992.6:c.*130_*132del (RAD21)	ENSP00000429342.2:n.*130_*132del
ENST00000522699.2:c.*130_*132del (RAD21)	ENSP00000428158.2:n.*130_*132del
ENST00000523986.6:n.4995_4997del (RAD21)
ENST00000685972.1:n.5329_5331del (RAD21)
ENST00000687122.1:n.4854_4856del (RAD21)
ENST00000687358.1:c.*130_*132del (RAD21)	ENSP00000509687.1:n.*130_*132del
ENST00000687902.1:c.*401_*403del (RAD21)	ENSP00000510729.1:n.*401_*403del
ENST00000689124.1:n.2240_2242del (RAD21)
ENST00000689154.1:n.1918_1920del (RAD21)
ENST00000690166.1:n.6895_6897del (RAD21)
ENST00000297338.7:c.*130_*132del (RAD21) MANE Select	ENSP00000297338.2:n.*130_*132del
ENST00000297338.6:c.*130_*132del (RAD21)	ENSP00000297338.2:n.*130_*132del
ENST00000517749.1:c.*130_*132del (RAD21)	ENSP00000430273.1:n.*130_*132del
ENST00000517820.1:c.189-1516_189-1514del (UTP23)	ENSP00000427767.1:n.189-1516_189-1514del
ENST00000518055.1:c.*130_*132del (RAD21)	ENSP00000428003.1:n.*130_*132del
ENST00000520733.5:c.46-1516_46-1514del (UTP23)	ENSP00000429384.1:n.46-1516_46-1514del
ENST00000521703.5:c.*93-1516_*93-1514del (UTP23)	ENSP00000428455.1:n.*93-1516_*93-1514del
ENST00000523986.5:c.*130_*132del (RAD21)	ENSP00000428513.1:n.*130_*132del
ENST00000524128.1:c.*93-1516_*93-1514del (UTP23)	ENSP00000430309.1:n.*93-1516_*93-1514del
NM_006265.2:c.*130_*132del , LRG_772t1:c.*130_*132del (RAD21)	NP_006256.1:n.*130_*132del
XR_928356.1:n.663-1516_663-1514del (UTP23)
NM_006265.3:c.*130_*132del (RAD21) MANE Select	NP_006256.1:n.*130_*132del