Canonical Allele Identifier: CA645554967

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.116847620_116847632dup , CM000670.2:g.116847620_116847632dup GRCh38
NC_000008.10:g.117859859_117859871dup , CM000670.1:g.117859859_117859871dup GRCh37
NC_000008.9:g.117929040_117929052dup NCBI36
NG_032862.1:g.32236_32248dup , LRG_772:g.32236_32248dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000517485.6:c.1765_1777dup (RAD21) ENSP00000427923.2:p.Ala593GlufsTer16
ENST00000517749.2:c.1765_1777dup (RAD21) ENSP00000430273.2:p.Ala593GlufsTer16
ENST00000519837.6:c.1765_1777dup (RAD21) ENSP00000430524.2:p.Ala593GlufsTer16
ENST00000520992.6:c.1765_1777dup (RAD21) ENSP00000429342.2:p.Ala593GlufsTer16
ENST00000522699.2:c.1765_1777dup (RAD21) ENSP00000428158.2:p.Ala593GlufsTer16
ENST00000523986.6:n.4734_4746dup (RAD21)
ENST00000685972.1:n.5068_5080dup (RAD21)
ENST00000687122.1:n.4593_4605dup (RAD21)
ENST00000687358.1:c.1765_1777dup (RAD21) ENSP00000509687.1:p.Ala593GlufsTer16
ENST00000687902.1:c.*140_*152dup (RAD21) ENSP00000510729.1:n.*140_*152dup
ENST00000689124.1:n.1979_1991dup (RAD21)
ENST00000689154.1:n.1657_1669dup (RAD21)
ENST00000690166.1:n.6634_6646dup (RAD21)
ENST00000297338.7:c.1765_1777dup (RAD21) MANE Select ENSP00000297338.2:p.Ala593GlufsTer16
ENST00000297338.6:c.1765_1777dup (RAD21) ENSP00000297338.2:p.Ala593GlufsTer16
ENST00000517749.1:c.79_91dup (RAD21) ENSP00000430273.1:p.Ala31GlufsTer16
ENST00000517820.1:c.189-1268_189-1256dup (UTP23) ENSP00000427767.1:n.189-1268_189-1256dup
ENST00000518055.1:c.400_412dup (RAD21) ENSP00000428003.1:p.Ala138GlufsTer16
ENST00000520733.5:c.46-1268_46-1256dup (UTP23) ENSP00000429384.1:n.46-1268_46-1256dup
ENST00000521703.5:c.*93-1268_*93-1256dup (UTP23) ENSP00000428455.1:n.*93-1268_*93-1256dup
ENST00000523986.5:c.277_289dup (RAD21) ENSP00000428513.1:p.Ala97GlufsTer16
ENST00000524128.1:c.*93-1268_*93-1256dup (UTP23) ENSP00000430309.1:n.*93-1268_*93-1256dup
NM_006265.2:c.1765_1777dup , LRG_772t1:c.1765_1777dup (RAD21) NP_006256.1:p.Ala593GlufsTer16
XR_928356.1:n.663-1268_663-1256dup (UTP23)
NM_006265.3:c.1765_1777dup (RAD21) MANE Select NP_006256.1:p.Ala593GlufsTer16