Canonical Allele Identifier: CA4852837

Gene: RAD21

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116852066A>C , CM000670.2:g.116852066A>C	GRCh38
NC_000008.10:g.117864305A>C , CM000670.1:g.117864305A>C	GRCh37
NC_000008.9:g.117933486A>C	NCBI36
NG_032862.1:g.27801T>G , LRG_772:g.27801T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006265.3:c.1352T>G MANE Select	NP_006256.1:p.Leu451Arg
ENST00000297338.7:c.1352T>G MANE Select	ENSP00000297338.2:p.Leu451Arg
NM_006265.2:c.1352T>G , LRG_772t1:c.1352T>G	NP_006256.1:p.Leu451Arg
ENST00000297338.6:c.1352T>G	ENSP00000297338.2:p.Leu451Arg
ENST00000517485.6:c.1352T>G	ENSP00000427923.2:p.Leu451Arg
ENST00000517749.2:c.1352T>G	ENSP00000430273.2:p.Leu451Arg
ENST00000518055.1:c.-14T>G	ENSP00000428003.1:n.-14T>G
ENST00000519837.6:c.1352T>G	ENSP00000430524.2:p.Leu451Arg
ENST00000520992.6:c.1352T>G	ENSP00000429342.2:p.Leu451Arg
ENST00000522699.2:c.1352T>G	ENSP00000428158.2:p.Leu451Arg
ENST00000523547.2:n.1462T>G
ENST00000523986.5:c.-1317T>G	ENSP00000428513.1:n.-1317T>G
ENST00000523986.6:n.3141T>G
ENST00000685972.1:n.1887T>G
ENST00000686622.1:n.1944T>G
ENST00000687122.1:n.4180T>G
ENST00000687358.1:c.1352T>G	ENSP00000509687.1:p.Leu451Arg
ENST00000687902.1:c.1352T>G	ENSP00000510729.1:p.Leu451Arg
ENST00000688033.1:n.3410T>G
ENST00000689124.1:n.1566T>G
ENST00000689504.1:n.1462T>G
ENST00000690166.1:n.2199T>G
ENST00000690189.1:n.5155T>G