Canonical Allele Identifier: CA4853021

Gene: RAD21

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116856761A>G , CM000670.2:g.116856761A>G	GRCh38
NC_000008.10:g.117869000A>G , CM000670.1:g.117869000A>G	GRCh37
NC_000008.9:g.117938181A>G	NCBI36
NG_032862.1:g.23106T>C , LRG_772:g.23106T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_006265.3:c.699T>C MANE Select	NP_006256.1:p.Leu233=
ENST00000297338.7:c.699T>C MANE Select	ENSP00000297338.2:p.Leu233=
NM_006265.2:c.699T>C , LRG_772t1:c.699T>C	NP_006256.1:p.Leu233=
ENST00000297338.6:c.699T>C	ENSP00000297338.2:p.Leu233=
ENST00000517485.6:c.699T>C	ENSP00000427923.2:p.Leu233=
ENST00000517749.2:c.699T>C	ENSP00000430273.2:p.Leu233=
ENST00000519837.6:c.699T>C	ENSP00000430524.2:p.Leu233=
ENST00000520992.6:c.699T>C	ENSP00000429342.2:p.Leu233=
ENST00000522699.2:c.699T>C	ENSP00000428158.2:p.Leu233=
ENST00000523547.2:n.809T>C
ENST00000523986.6:n.500T>C
ENST00000685972.1:n.782T>C
ENST00000686622.1:n.1291T>C
ENST00000687122.1:n.3527T>C
ENST00000687358.1:c.699T>C	ENSP00000509687.1:p.Leu233=
ENST00000687902.1:c.699T>C	ENSP00000510729.1:p.Leu233=
ENST00000688033.1:n.769T>C
ENST00000689124.1:n.913T>C
ENST00000689504.1:n.809T>C
ENST00000690166.1:n.1094T>C
ENST00000690189.1:n.2514T>C