Canonical Allele Identifier: CA372005821

Gene: RAD21

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116857269A>G , CM000670.2:g.116857269A>G	GRCh38
NC_000008.10:g.117869508A>G , CM000670.1:g.117869508A>G	GRCh37
NC_000008.9:g.117938689A>G	NCBI36
NG_032862.1:g.22598T>C , LRG_772:g.22598T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_006265.3:c.686T>C MANE Select	NP_006256.1:p.Leu229Ser
ENST00000297338.7:c.686T>C MANE Select	ENSP00000297338.2:p.Leu229Ser
NM_006265.2:c.686T>C , LRG_772t1:c.686T>C	NP_006256.1:p.Leu229Ser
ENST00000297338.6:c.686T>C	ENSP00000297338.2:p.Leu229Ser
ENST00000517485.6:c.686T>C	ENSP00000427923.2:p.Leu229Ser
ENST00000517749.2:c.686T>C	ENSP00000430273.2:p.Leu229Ser
ENST00000519837.6:c.686T>C	ENSP00000430524.2:p.Leu229Ser
ENST00000520992.6:c.686T>C	ENSP00000429342.2:p.Leu229Ser
ENST00000522699.2:c.686T>C	ENSP00000428158.2:p.Leu229Ser
ENST00000523547.2:n.796T>C
ENST00000685972.1:n.769T>C
ENST00000686622.1:n.783T>C
ENST00000687122.1:n.3514T>C
ENST00000687358.1:c.686T>C	ENSP00000509687.1:p.Leu229Ser
ENST00000687902.1:c.686T>C	ENSP00000510729.1:p.Leu229Ser
ENST00000688033.1:n.756T>C
ENST00000689124.1:n.900T>C
ENST00000689504.1:n.796T>C
ENST00000690166.1:n.586T>C
ENST00000690189.1:n.2501T>C