Canonical Allele Identifier: CA584814773

Gene: RAD21 UTP23

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116849042G>A , CM000670.2:g.116849042G>A	GRCh38
NC_000008.10:g.117861281G>A , CM000670.1:g.117861281G>A	GRCh37
NC_000008.9:g.117930462G>A	NCBI36
NG_032862.1:g.30825C>T , LRG_772:g.30825C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006265.3:c.1621-13C>T (RAD21) MANE Select	NP_006256.1:n.1621-13C>T
ENST00000297338.7:c.1621-13C>T (RAD21) MANE Select	ENSP00000297338.2:n.1621-13C>T
NM_006265.2:c.1621-13C>T , LRG_772t1:c.1621-13C>T (RAD21)	NP_006256.1:n.1621-13C>T
ENST00000297338.6:c.1621-13C>T (RAD21)	ENSP00000297338.2:n.1621-13C>T
ENST00000517485.6:c.1621-13C>T (RAD21)	ENSP00000427923.2:n.1621-13C>T
ENST00000517749.1:c.-79C>T (RAD21)	ENSP00000430273.1:n.-79C>T
ENST00000517749.2:c.1621-13C>T (RAD21)	ENSP00000430273.2:n.1621-13C>T
ENST00000517820.1:c.*25G>A (UTP23)	ENSP00000427767.1:n.*25G>A
ENST00000518055.1:c.256-13C>T (RAD21)	ENSP00000428003.1:n.256-13C>T
ENST00000519837.6:c.1621-13C>T (RAD21)	ENSP00000430524.2:n.1621-13C>T
ENST00000520733.5:c.*5G>A (UTP23)	ENSP00000429384.1:n.*5G>A
ENST00000520992.6:c.1621-13C>T (RAD21)	ENSP00000429342.2:n.1621-13C>T
ENST00000521703.5:c.*247G>A (UTP23)	ENSP00000428455.1:n.*247G>A
ENST00000522699.2:c.1621-13C>T (RAD21)	ENSP00000428158.2:n.1621-13C>T
ENST00000523547.2:n.1731-13C>T (RAD21)
ENST00000523986.5:c.133-13C>T (RAD21)	ENSP00000428513.1:n.133-13C>T
ENST00000523986.6:n.4590-13C>T (RAD21)
ENST00000524128.1:c.*247G>A (UTP23)	ENSP00000430309.1:n.*247G>A
ENST00000685972.1:n.4911C>T (RAD21)
ENST00000686622.1:n.4968C>T (RAD21)
ENST00000687122.1:n.4449-13C>T (RAD21)
ENST00000687358.1:c.1621-13C>T (RAD21)	ENSP00000509687.1:n.1621-13C>T
ENST00000687902.1:c.1633C>T (RAD21)	ENSP00000510729.1:p.His545Tyr
ENST00000688033.1:n.6434C>T (RAD21)
ENST00000689124.1:n.1835-13C>T (RAD21)
ENST00000689154.1:n.259-13C>T (RAD21)
ENST00000690166.1:n.5223C>T (RAD21)
ENST00000690189.1:n.8179C>T (RAD21)