Canonical Allele Identifier: CA371988706

Gene: RAD21 UTP23

Linked Data

• dbSNP Id: rs775266057
• MyVariant Identifiers: chr8:g.117859771C>A (hg19) ; chr8:g.116847532C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116847532C>A , CM000670.2:g.116847532C>A	GRCh38
NC_000008.10:g.117859771C>A , CM000670.1:g.117859771C>A	GRCh37
NC_000008.9:g.117928952C>A	NCBI36
NG_032862.1:g.32335G>T , LRG_772:g.32335G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517485.6:c.1864G>T (RAD21)	ENSP00000427923.2:p.Ala622Ser
ENST00000517749.2:c.1864G>T (RAD21)	ENSP00000430273.2:p.Ala622Ser
ENST00000519837.6:c.1864G>T (RAD21)	ENSP00000430524.2:p.Ala622Ser
ENST00000520992.6:c.1864G>T (RAD21)	ENSP00000429342.2:p.Ala622Ser
ENST00000522699.2:c.1864G>T (RAD21)	ENSP00000428158.2:p.Ala622Ser
ENST00000523986.6:n.4833G>T (RAD21)
ENST00000685972.1:n.5167G>T (RAD21)
ENST00000687122.1:n.4692G>T (RAD21)
ENST00000687358.1:c.1864G>T (RAD21)	ENSP00000509687.1:p.Ala622Ser
ENST00000687902.1:c.*239G>T (RAD21)	ENSP00000510729.1:n.*239G>T
ENST00000689124.1:n.2078G>T (RAD21)
ENST00000689154.1:n.1756G>T (RAD21)
ENST00000690166.1:n.6733G>T (RAD21)
ENST00000297338.7:c.1864G>T (RAD21) MANE Select	ENSP00000297338.2:p.Ala622Ser
ENST00000297338.6:c.1864G>T (RAD21)	ENSP00000297338.2:p.Ala622Ser
ENST00000517749.1:c.178G>T (RAD21)	ENSP00000430273.1:p.Ala60Ser
ENST00000517820.1:c.189-1356C>A (UTP23)	ENSP00000427767.1:n.189-1356C>A
ENST00000518055.1:c.499G>T (RAD21)	ENSP00000428003.1:p.Ala167Ser
ENST00000520733.5:c.46-1356C>A (UTP23)	ENSP00000429384.1:n.46-1356C>A
ENST00000521703.5:c.*93-1356C>A (UTP23)	ENSP00000428455.1:n.*93-1356C>A
ENST00000523986.5:c.376G>T (RAD21)	ENSP00000428513.1:p.Ala126Ser
ENST00000524128.1:c.*93-1356C>A (UTP23)	ENSP00000430309.1:n.*93-1356C>A
NM_006265.2:c.1864G>T , LRG_772t1:c.1864G>T (RAD21)	NP_006256.1:p.Ala622Ser
XR_928356.1:n.663-1356C>A (UTP23)
NM_006265.3:c.1864G>T (RAD21) MANE Select	NP_006256.1:p.Ala622Ser