Canonical Allele Identifier: CA1813513144
Gene: RAD21 HGNC NCBI

Linked Data

dbSNP Id: rs16889040

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.116866452C>A , CM000670.2:g.116866452C>A GRCh38
NC_000008.10:g.117878691C>A , CM000670.1:g.117878691C>A GRCh37
NC_000008.9:g.117947872C>A NCBI36
NG_032862.1:g.13415G>T , LRG_772:g.13415G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000517485.6:c.144+134G>T ENSP00000427923.2:n.144+134G>T
ENST00000517749.2:c.144+134G>T ENSP00000430273.2:n.144+134G>T
ENST00000519469.2:n.406+134G>T
ENST00000519837.6:c.144+134G>T ENSP00000430524.2:n.144+134G>T
ENST00000520992.6:c.144+134G>T ENSP00000429342.2:n.144+134G>T
ENST00000522699.2:c.144+134G>T ENSP00000428158.2:n.144+134G>T
ENST00000523547.2:n.254+134G>T
ENST00000685972.1:n.227+134G>T
ENST00000686622.1:n.241+134G>T
ENST00000687358.1:c.144+134G>T ENSP00000509687.1:n.144+134G>T
ENST00000687902.1:c.144+134G>T ENSP00000510729.1:n.144+134G>T
ENST00000688033.1:n.214+134G>T
ENST00000689504.1:n.254+134G>T
ENST00000690166.1:n.44+134G>T
ENST00000297338.7:c.144+134G>T MANE Select ENSP00000297338.2:n.144+134G>T
ENST00000297338.6:c.144+134G>T ENSP00000297338.2:n.144+134G>T
ENST00000517485.5:c.144+134G>T ENSP00000427923.1:n.144+134G>T
ENST00000519469.1:n.406+134G>T
ENST00000519837.5:c.144+134G>T ENSP00000430524.1:n.144+134G>T
ENST00000520992.5:c.144+134G>T ENSP00000429342.1:n.144+134G>T
ENST00000522699.1:c.144+134G>T ENSP00000428158.1:n.144+134G>T
ENST00000523547.1:n.386+134G>T
NM_006265.2:c.144+134G>T , LRG_772t1:c.144+134G>T NP_006256.1:n.144+134G>T
NM_006265.3:c.144+134G>T MANE Select NP_006256.1:n.144+134G>T