Canonical Allele Identifier: CA4853051

Gene: RAD21

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116857391A>C , CM000670.2:g.116857391A>C	GRCh38
NC_000008.10:g.117869630A>C , CM000670.1:g.117869630A>C	GRCh37
NC_000008.9:g.117938811A>C	NCBI36
NG_032862.1:g.22476T>G , LRG_772:g.22476T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006265.3:c.564T>G MANE Select	NP_006256.1:p.Thr188=
ENST00000297338.7:c.564T>G MANE Select	ENSP00000297338.2:p.Thr188=
NM_006265.2:c.564T>G , LRG_772t1:c.564T>G	NP_006256.1:p.Thr188=
ENST00000297338.6:c.564T>G	ENSP00000297338.2:p.Thr188=
ENST00000517485.5:c.564T>G	ENSP00000427923.1:p.Thr188=
ENST00000517485.6:c.564T>G	ENSP00000427923.2:p.Thr188=
ENST00000517749.2:c.564T>G	ENSP00000430273.2:p.Thr188=
ENST00000519837.6:c.564T>G	ENSP00000430524.2:p.Thr188=
ENST00000520992.5:c.564T>G	ENSP00000429342.1:p.Thr188=
ENST00000520992.6:c.564T>G	ENSP00000429342.2:p.Thr188=
ENST00000522699.2:c.564T>G	ENSP00000428158.2:p.Thr188=
ENST00000523547.1:n.806T>G
ENST00000523547.2:n.674T>G
ENST00000685972.1:n.647T>G
ENST00000686622.1:n.661T>G
ENST00000687122.1:n.3392T>G
ENST00000687358.1:c.564T>G	ENSP00000509687.1:p.Thr188=
ENST00000687902.1:c.564T>G	ENSP00000510729.1:p.Thr188=
ENST00000688033.1:n.634T>G
ENST00000689124.1:n.778T>G
ENST00000689504.1:n.674T>G
ENST00000690166.1:n.464T>G
ENST00000690189.1:n.2379T>G