Canonical Allele Identifier: CA4852680

Gene: RAD21 UTP23

Linked Data

• dbSNP Id: rs547272219
• ExAC: 8:117859829 A / T
• gnomAD v2: 8-117859829-A-T
• gnomAD v3: 8-116847590-A-T
• gnomAD v4: 8-116847590-A-T
• MyVariant Identifiers: chr8:g.117859829A>T (hg19) ; chr8:g.116847590A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116847590A>T , CM000670.2:g.116847590A>T	GRCh38
NC_000008.10:g.117859829A>T , CM000670.1:g.117859829A>T	GRCh37
NC_000008.9:g.117929010A>T	NCBI36
NG_032862.1:g.32277T>A , LRG_772:g.32277T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000517485.6:c.1806T>A (RAD21)	ENSP00000427923.2:p.Val602=
ENST00000517749.2:c.1806T>A (RAD21)	ENSP00000430273.2:p.Val602=
ENST00000519837.6:c.1806T>A (RAD21)	ENSP00000430524.2:p.Val602=
ENST00000520992.6:c.1806T>A (RAD21)	ENSP00000429342.2:p.Val602=
ENST00000522699.2:c.1806T>A (RAD21)	ENSP00000428158.2:p.Val602=
ENST00000523986.6:n.4775T>A (RAD21)
ENST00000685972.1:n.5109T>A (RAD21)
ENST00000687122.1:n.4634T>A (RAD21)
ENST00000687358.1:c.1806T>A (RAD21)	ENSP00000509687.1:p.Val602=
ENST00000687902.1:c.*181T>A (RAD21)	ENSP00000510729.1:n.*181T>A
ENST00000689124.1:n.2020T>A (RAD21)
ENST00000689154.1:n.1698T>A (RAD21)
ENST00000690166.1:n.6675T>A (RAD21)
ENST00000297338.7:c.1806T>A (RAD21) MANE Select	ENSP00000297338.2:p.Val602=
ENST00000297338.6:c.1806T>A (RAD21)	ENSP00000297338.2:p.Val602=
ENST00000517749.1:c.120T>A (RAD21)	ENSP00000430273.1:p.Val40=
ENST00000517820.1:c.189-1298A>T (UTP23)	ENSP00000427767.1:n.189-1298A>T
ENST00000518055.1:c.441T>A (RAD21)	ENSP00000428003.1:p.Val147=
ENST00000520733.5:c.46-1298A>T (UTP23)	ENSP00000429384.1:n.46-1298A>T
ENST00000521703.5:c.*93-1298A>T (UTP23)	ENSP00000428455.1:n.*93-1298A>T
ENST00000523986.5:c.318T>A (RAD21)	ENSP00000428513.1:p.Val106=
ENST00000524128.1:c.*93-1298A>T (UTP23)	ENSP00000430309.1:n.*93-1298A>T
NM_006265.2:c.1806T>A , LRG_772t1:c.1806T>A (RAD21)	NP_006256.1:p.Val602=
XR_928356.1:n.663-1298A>T (UTP23)
NM_006265.3:c.1806T>A (RAD21) MANE Select	NP_006256.1:p.Val602=