Canonical Allele Identifier: CA4852695

Gene: RAD21 UTP23

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116847690C>T , CM000670.2:g.116847690C>T	GRCh38
NC_000008.10:g.117859929C>T , CM000670.1:g.117859929C>T	GRCh37
NC_000008.9:g.117929110C>T	NCBI36
NG_032862.1:g.32177G>A , LRG_772:g.32177G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006265.3:c.1706G>A (RAD21) MANE Select	NP_006256.1:p.Arg569His
ENST00000297338.7:c.1706G>A (RAD21) MANE Select	ENSP00000297338.2:p.Arg569His
NM_006265.2:c.1706G>A , LRG_772t1:c.1706G>A (RAD21)	NP_006256.1:p.Arg569His
ENST00000297338.6:c.1706G>A (RAD21)	ENSP00000297338.2:p.Arg569His
ENST00000517485.6:c.1706G>A (RAD21)	ENSP00000427923.2:p.Arg569His
ENST00000517749.1:c.20G>A (RAD21)	ENSP00000430273.1:p.Arg7His
ENST00000517749.2:c.1706G>A (RAD21)	ENSP00000430273.2:p.Arg569His
ENST00000517820.1:c.189-1198C>T (UTP23)	ENSP00000427767.1:n.189-1198C>T
ENST00000518055.1:c.341G>A (RAD21)	ENSP00000428003.1:p.Arg114His
ENST00000519837.6:c.1706G>A (RAD21)	ENSP00000430524.2:p.Arg569His
ENST00000520733.5:c.46-1198C>T (UTP23)	ENSP00000429384.1:n.46-1198C>T
ENST00000520992.6:c.1706G>A (RAD21)	ENSP00000429342.2:p.Arg569His
ENST00000521703.5:c.*93-1198C>T (UTP23)	ENSP00000428455.1:n.*93-1198C>T
ENST00000522699.2:c.1706G>A (RAD21)	ENSP00000428158.2:p.Arg569His
ENST00000523986.5:c.218G>A (RAD21)	ENSP00000428513.1:p.Arg73His
ENST00000523986.6:n.4675G>A (RAD21)
ENST00000524128.1:c.*93-1198C>T (UTP23)	ENSP00000430309.1:n.*93-1198C>T
ENST00000685972.1:n.5009G>A (RAD21)
ENST00000687122.1:n.4534G>A (RAD21)
ENST00000687358.1:c.1706G>A (RAD21)	ENSP00000509687.1:p.Arg569His
ENST00000687902.1:c.*81G>A (RAD21)	ENSP00000510729.1:n.*81G>A
ENST00000689124.1:n.1920G>A (RAD21)
ENST00000689154.1:n.1598G>A (RAD21)
ENST00000690166.1:n.6575G>A (RAD21)
XR_928356.1:n.663-1198C>T (UTP23)