Canonical Allele Identifier: CA1813520528

Gene: RAD21 UTP23

Linked Data

• dbSNP Id: rs1812266724

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116847186T>C , CM000670.2:g.116847186T>C	GRCh38
NC_000008.10:g.117859425T>C , CM000670.1:g.117859425T>C	GRCh37
NC_000008.9:g.117928606T>C	NCBI36
NG_032862.1:g.32681A>G , LRG_772:g.32681A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517485.6:c.*314A>G (RAD21)	ENSP00000427923.2:n.*314A>G
ENST00000517749.2:c.*314A>G (RAD21)	ENSP00000430273.2:n.*314A>G
ENST00000519837.6:c.*314A>G (RAD21)	ENSP00000430524.2:n.*314A>G
ENST00000520992.6:c.*314A>G (RAD21)	ENSP00000429342.2:n.*314A>G
ENST00000522699.2:c.*314A>G (RAD21)	ENSP00000428158.2:n.*314A>G
ENST00000523986.6:n.5179A>G (RAD21)
ENST00000685972.1:n.5513A>G (RAD21)
ENST00000687122.1:n.5038A>G (RAD21)
ENST00000687358.1:c.*314A>G (RAD21)	ENSP00000509687.1:n.*314A>G
ENST00000687902.1:c.*585A>G (RAD21)	ENSP00000510729.1:n.*585A>G
ENST00000689124.1:n.2424A>G (RAD21)
ENST00000689154.1:n.2102A>G (RAD21)
ENST00000690166.1:n.7079A>G (RAD21)
ENST00000297338.7:c.*314A>G (RAD21) MANE Select	ENSP00000297338.2:n.*314A>G
ENST00000297338.6:c.*314A>G (RAD21)	ENSP00000297338.2:n.*314A>G
ENST00000517820.1:c.189-1702T>C (UTP23)	ENSP00000427767.1:n.189-1702T>C
ENST00000520733.5:c.46-1702T>C (UTP23)	ENSP00000429384.1:n.46-1702T>C
ENST00000521703.5:c.*93-1702T>C (UTP23)	ENSP00000428455.1:n.*93-1702T>C
ENST00000523986.5:c.*314A>G (RAD21)	ENSP00000428513.1:n.*314A>G
ENST00000524128.1:c.*93-1702T>C (UTP23)	ENSP00000430309.1:n.*93-1702T>C
NM_006265.2:c.*314A>G , LRG_772t1:c.*314A>G (RAD21)	NP_006256.1:n.*314A>G
XR_928356.1:n.663-1702T>C (UTP23)
NM_006265.3:c.*314A>G (RAD21) MANE Select	NP_006256.1:n.*314A>G