Canonical Allele Identifier: CA4853024

Gene: RAD21

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116856786G>T , CM000670.2:g.116856786G>T	GRCh38
NC_000008.10:g.117869025G>T , CM000670.1:g.117869025G>T	GRCh37
NC_000008.9:g.117938206G>T	NCBI36
NG_032862.1:g.23081C>A , LRG_772:g.23081C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006265.3:c.689-15C>A MANE Select	NP_006256.1:n.689-15C>A
ENST00000297338.7:c.689-15C>A MANE Select	ENSP00000297338.2:n.689-15C>A
NM_006265.2:c.689-15C>A , LRG_772t1:c.689-15C>A	NP_006256.1:n.689-15C>A
ENST00000297338.6:c.689-15C>A	ENSP00000297338.2:n.689-15C>A
ENST00000517485.6:c.689-15C>A	ENSP00000427923.2:n.689-15C>A
ENST00000517749.2:c.689-15C>A	ENSP00000430273.2:n.689-15C>A
ENST00000519837.6:c.689-15C>A	ENSP00000430524.2:n.689-15C>A
ENST00000520992.6:c.689-15C>A	ENSP00000429342.2:n.689-15C>A
ENST00000522699.2:c.689-15C>A	ENSP00000428158.2:n.689-15C>A
ENST00000523547.2:n.799-15C>A
ENST00000523986.6:n.475C>A
ENST00000685972.1:n.772-15C>A
ENST00000686622.1:n.1266C>A
ENST00000687122.1:n.3517-15C>A
ENST00000687358.1:c.689-15C>A	ENSP00000509687.1:n.689-15C>A
ENST00000687902.1:c.689-15C>A	ENSP00000510729.1:n.689-15C>A
ENST00000688033.1:n.759-15C>A
ENST00000689124.1:n.903-15C>A
ENST00000689504.1:n.799-15C>A
ENST00000690166.1:n.1069C>A
ENST00000690189.1:n.2504-15C>A