Canonical Allele Identifier: CA184264481

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.116849023C>T , CM000670.2:g.116849023C>T GRCh38
NC_000008.10:g.117861262C>T , CM000670.1:g.117861262C>T GRCh37
NC_000008.9:g.117930443C>T NCBI36
NG_032862.1:g.30844G>A , LRG_772:g.30844G>A

Transcript Alleles

HGVS Amino-acid Change
NM_006265.3:c.1627G>A (RAD21) MANE Select NP_006256.1:p.Asp543Asn
ENST00000297338.7:c.1627G>A (RAD21) MANE Select ENSP00000297338.2:p.Asp543Asn
NM_006265.2:c.1627G>A , LRG_772t1:c.1627G>A (RAD21) NP_006256.1:p.Asp543Asn
ENST00000297338.6:c.1627G>A (RAD21) ENSP00000297338.2:p.Asp543Asn
ENST00000517485.6:c.1627G>A (RAD21) ENSP00000427923.2:p.Asp543Asn
ENST00000517749.1:c.-60G>A (RAD21) ENSP00000430273.1:n.-60G>A
ENST00000517749.2:c.1627G>A (RAD21) ENSP00000430273.2:p.Asp543Asn
ENST00000517820.1:c.*6C>T (UTP23) ENSP00000427767.1:n.*6C>T
ENST00000518055.1:c.262G>A (RAD21) ENSP00000428003.1:p.Asp88Asn
ENST00000519837.6:c.1627G>A (RAD21) ENSP00000430524.2:p.Asp543Asn
ENST00000520733.5:c.181C>T (UTP23) ENSP00000429384.1:p.Leu61Phe
ENST00000520992.6:c.1627G>A (RAD21) ENSP00000429342.2:p.Asp543Asn
ENST00000521703.5:c.*228C>T (UTP23) ENSP00000428455.1:n.*228C>T
ENST00000522699.2:c.1627G>A (RAD21) ENSP00000428158.2:p.Asp543Asn
ENST00000523547.2:n.1737G>A (RAD21)
ENST00000523986.5:c.139G>A (RAD21) ENSP00000428513.1:p.Asp47Asn
ENST00000523986.6:n.4596G>A (RAD21)
ENST00000524128.1:c.*228C>T (UTP23) ENSP00000430309.1:n.*228C>T
ENST00000685972.1:n.4930G>A (RAD21)
ENST00000686622.1:n.4987G>A (RAD21)
ENST00000687122.1:n.4455G>A (RAD21)
ENST00000687358.1:c.1627G>A (RAD21) ENSP00000509687.1:p.Asp543Asn
ENST00000687902.1:c.*2G>A (RAD21) ENSP00000510729.1:n.*2G>A
ENST00000688033.1:n.6453G>A (RAD21)
ENST00000689124.1:n.1841G>A (RAD21)
ENST00000689154.1:n.265G>A (RAD21)
ENST00000690166.1:n.5242G>A (RAD21)
ENST00000690189.1:n.8198G>A (RAD21)