Canonical Allele Identifier: CA4852960

Gene: RAD21

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116856235T>C , CM000670.2:g.116856235T>C	GRCh38
NC_000008.10:g.117868474T>C , CM000670.1:g.117868474T>C	GRCh37
NC_000008.9:g.117937655T>C	NCBI36
NG_032862.1:g.23632A>G , LRG_772:g.23632A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006265.3:c.868A>G MANE Select	NP_006256.1:p.Met290Val
ENST00000297338.7:c.868A>G MANE Select	ENSP00000297338.2:p.Met290Val
NM_006265.2:c.868A>G , LRG_772t1:c.868A>G	NP_006256.1:p.Met290Val
ENST00000297338.6:c.868A>G	ENSP00000297338.2:p.Met290Val
ENST00000517485.6:c.868A>G	ENSP00000427923.2:p.Met290Val
ENST00000517749.2:c.868A>G	ENSP00000430273.2:p.Met290Val
ENST00000519837.6:c.868A>G	ENSP00000430524.2:p.Met290Val
ENST00000520992.6:c.868A>G	ENSP00000429342.2:p.Met290Val
ENST00000522699.2:c.868A>G	ENSP00000428158.2:p.Met290Val
ENST00000523547.2:n.978A>G
ENST00000523986.6:n.669A>G
ENST00000685972.1:n.951A>G
ENST00000686622.1:n.1460A>G
ENST00000687122.1:n.3696A>G
ENST00000687358.1:c.868A>G	ENSP00000509687.1:p.Met290Val
ENST00000687902.1:c.868A>G	ENSP00000510729.1:p.Met290Val
ENST00000688033.1:n.938A>G
ENST00000689124.1:n.1082A>G
ENST00000689504.1:n.978A>G
ENST00000690166.1:n.1263A>G
ENST00000690189.1:n.2683A>G