Canonical Allele Identifier: CA462497884

Gene: RAD21 UTP23

Linked Data

• MyVariant Identifiers: chr8:g.117859856A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116847617A>G , CM000670.2:g.116847617A>G	GRCh38
NC_000008.10:g.117859856A>G , CM000670.1:g.117859856A>G	GRCh37
NC_000008.9:g.117929037A>G	NCBI36
NG_032862.1:g.32250T>C , LRG_772:g.32250T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517485.6:c.1779T>C (RAD21)	ENSP00000427923.2:p.Ala593=
ENST00000517749.2:c.1779T>C (RAD21)	ENSP00000430273.2:p.Ala593=
ENST00000519837.6:c.1779T>C (RAD21)	ENSP00000430524.2:p.Ala593=
ENST00000520992.6:c.1779T>C (RAD21)	ENSP00000429342.2:p.Ala593=
ENST00000522699.2:c.1779T>C (RAD21)	ENSP00000428158.2:p.Ala593=
ENST00000523986.6:n.4748T>C (RAD21)
ENST00000685972.1:n.5082T>C (RAD21)
ENST00000687122.1:n.4607T>C (RAD21)
ENST00000687358.1:c.1779T>C (RAD21)	ENSP00000509687.1:p.Ala593=
ENST00000687902.1:c.*154T>C (RAD21)	ENSP00000510729.1:n.*154T>C
ENST00000689124.1:n.1993T>C (RAD21)
ENST00000689154.1:n.1671T>C (RAD21)
ENST00000690166.1:n.6648T>C (RAD21)
ENST00000297338.7:c.1779T>C (RAD21) MANE Select	ENSP00000297338.2:p.Ala593=
ENST00000297338.6:c.1779T>C (RAD21)	ENSP00000297338.2:p.Ala593=
ENST00000517749.1:c.93T>C (RAD21)	ENSP00000430273.1:p.Ala31=
ENST00000517820.1:c.189-1271A>G (UTP23)	ENSP00000427767.1:n.189-1271A>G
ENST00000518055.1:c.414T>C (RAD21)	ENSP00000428003.1:p.Ala138=
ENST00000520733.5:c.46-1271A>G (UTP23)	ENSP00000429384.1:n.46-1271A>G
ENST00000521703.5:c.*93-1271A>G (UTP23)	ENSP00000428455.1:n.*93-1271A>G
ENST00000523986.5:c.291T>C (RAD21)	ENSP00000428513.1:p.Ala97=
ENST00000524128.1:c.*93-1271A>G (UTP23)	ENSP00000430309.1:n.*93-1271A>G
NM_006265.2:c.1779T>C , LRG_772t1:c.1779T>C (RAD21)	NP_006256.1:p.Ala593=
XR_928356.1:n.663-1271A>G (UTP23)
NM_006265.3:c.1779T>C (RAD21) MANE Select	NP_006256.1:p.Ala593=