Canonical Allele Identifier: CA2697550112

Gene: RAD21

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116857272del , CM000670.2:g.116857272del	GRCh38
NC_000008.10:g.117869511del , CM000670.1:g.117869511del	GRCh37
NC_000008.9:g.117938692del	NCBI36
NG_032862.1:g.22595del , LRG_772:g.22595del

Transcript Alleles

HGVS	Amino-acid Change
NM_006265.3:c.683del MANE Select	NP_006256.1:p.Ile228AsnfsTer2
ENST00000297338.7:c.683del MANE Select	ENSP00000297338.2:p.Ile228AsnfsTer2
NM_006265.2:c.683del , LRG_772t1:c.683del	NP_006256.1:p.Ile228AsnfsTer2
ENST00000297338.6:c.683del	ENSP00000297338.2:p.Ile228AsnfsTer2
ENST00000517485.6:c.683del	ENSP00000427923.2:p.Ile228AsnfsTer2
ENST00000517749.2:c.683del	ENSP00000430273.2:p.Ile228AsnfsTer2
ENST00000519837.6:c.683del	ENSP00000430524.2:p.Ile228AsnfsTer2
ENST00000520992.5:c.683del	ENSP00000429342.1:p.Ile228=
ENST00000520992.6:c.683del	ENSP00000429342.2:p.Ile228AsnfsTer2
ENST00000522699.2:c.683del	ENSP00000428158.2:p.Ile228AsnfsTer2
ENST00000523547.2:n.793del
ENST00000685972.1:n.766del
ENST00000686622.1:n.780del
ENST00000687122.1:n.3511del
ENST00000687358.1:c.683del	ENSP00000509687.1:p.Ile228AsnfsTer2
ENST00000687902.1:c.683del	ENSP00000510729.1:p.Ile228AsnfsTer2
ENST00000688033.1:n.753del
ENST00000689124.1:n.897del
ENST00000689504.1:n.793del
ENST00000690166.1:n.583del
ENST00000690189.1:n.2498del