Canonical Allele Identifier: CA372012277

Gene: RAD21

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116866721G>C , CM000670.2:g.116866721G>C	GRCh38
NC_000008.10:g.117878960G>C , CM000670.1:g.117878960G>C	GRCh37
NC_000008.9:g.117948141G>C	NCBI36
NG_032862.1:g.13146C>G , LRG_772:g.13146C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006265.3:c.9C>G MANE Select	NP_006256.1:p.Tyr3Ter
ENST00000297338.7:c.9C>G MANE Select	ENSP00000297338.2:p.Tyr3Ter
NM_006265.2:c.9C>G , LRG_772t1:c.9C>G	NP_006256.1:p.Tyr3Ter
ENST00000297338.6:c.9C>G	ENSP00000297338.2:p.Tyr3Ter
ENST00000517485.5:c.9C>G	ENSP00000427923.1:p.Tyr3Ter
ENST00000517485.6:c.9C>G	ENSP00000427923.2:p.Tyr3Ter
ENST00000517749.2:c.9C>G	ENSP00000430273.2:p.Tyr3Ter
ENST00000519469.1:n.271C>G
ENST00000519469.2:n.271C>G
ENST00000519837.5:c.9C>G	ENSP00000430524.1:p.Tyr3Ter
ENST00000519837.6:c.9C>G	ENSP00000430524.2:p.Tyr3Ter
ENST00000520992.5:c.9C>G	ENSP00000429342.1:p.Tyr3Ter
ENST00000520992.6:c.9C>G	ENSP00000429342.2:p.Tyr3Ter
ENST00000522699.1:c.9C>G	ENSP00000428158.1:p.Tyr3Ter
ENST00000522699.2:c.9C>G	ENSP00000428158.2:p.Tyr3Ter
ENST00000523547.1:n.251C>G
ENST00000523547.2:n.119C>G
ENST00000685972.1:n.92C>G
ENST00000686622.1:n.106C>G
ENST00000687358.1:c.9C>G	ENSP00000509687.1:p.Tyr3Ter
ENST00000687902.1:c.9C>G	ENSP00000510729.1:p.Tyr3Ter
ENST00000688033.1:n.79C>G
ENST00000689504.1:n.119C>G