Canonical Allele Identifier: CA846126690

Gene: RAD21 UTP23

Linked Data

• dbSNP Id: rs1286892902
• gnomAD v3: 8-116847173-AAG-A
• gnomAD v4: 8-116847173-AAG-A
• MyVariant Identifiers: chr8:g.117859413_117859414del (hg19) ; chr8:g.116847174_116847175del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116847175_116847176del , CM000670.2:g.116847175_116847176del	GRCh38
NC_000008.10:g.117859414_117859415del , CM000670.1:g.117859414_117859415del	GRCh37
NC_000008.9:g.117928595_117928596del	NCBI36
NG_032862.1:g.32692_32693del , LRG_772:g.32692_32693del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517485.6:c.*325_*326del (RAD21)	ENSP00000427923.2:n.*325_*326del
ENST00000517749.2:c.*325_*326del (RAD21)	ENSP00000430273.2:n.*325_*326del
ENST00000519837.6:c.*325_*326del (RAD21)	ENSP00000430524.2:n.*325_*326del
ENST00000520992.6:c.*325_*326del (RAD21)	ENSP00000429342.2:n.*325_*326del
ENST00000522699.2:c.*325_*326del (RAD21)	ENSP00000428158.2:n.*325_*326del
ENST00000523986.6:n.5190_5191del (RAD21)
ENST00000685972.1:n.5524_5525del (RAD21)
ENST00000687122.1:n.5049_5050del (RAD21)
ENST00000687358.1:c.*325_*326del (RAD21)	ENSP00000509687.1:n.*325_*326del
ENST00000687902.1:c.*596_*597del (RAD21)	ENSP00000510729.1:n.*596_*597del
ENST00000689124.1:n.2435_2436del (RAD21)
ENST00000689154.1:n.2113_2114del (RAD21)
ENST00000690166.1:n.7090_7091del (RAD21)
ENST00000297338.7:c.*325_*326del (RAD21) MANE Select	ENSP00000297338.2:n.*325_*326del
ENST00000297338.6:c.*325_*326del (RAD21)	ENSP00000297338.2:n.*325_*326del
ENST00000517820.1:c.189-1713_189-1712del (UTP23)	ENSP00000427767.1:n.189-1713_189-1712del
ENST00000520733.5:c.46-1713_46-1712del (UTP23)	ENSP00000429384.1:n.46-1713_46-1712del
ENST00000521703.5:c.*93-1713_*93-1712del (UTP23)	ENSP00000428455.1:n.*93-1713_*93-1712del
ENST00000523986.5:c.*325_*326del (RAD21)	ENSP00000428513.1:n.*325_*326del
ENST00000524128.1:c.*93-1713_*93-1712del (UTP23)	ENSP00000430309.1:n.*93-1713_*93-1712del
NM_006265.2:c.*325_*326del , LRG_772t1:c.*325_*326del (RAD21)	NP_006256.1:n.*325_*326del
XR_928356.1:n.663-1713_663-1712del (UTP23)
NM_006265.3:c.*325_*326del (RAD21) MANE Select	NP_006256.1:n.*325_*326del