Canonical Allele Identifier: CA1813520805

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.116847367_116847370delinsTGAA , CM000670.2:g.116847367_116847370delinsTGAA GRCh38
NC_000008.10:g.117859606_117859609delinsTGAA , CM000670.1:g.117859606_117859609delinsTGAA GRCh37
NC_000008.9:g.117928787_117928790delinsTGAA NCBI36
NG_032862.1:g.32497_32500delinsTTCA , LRG_772:g.32497_32500delinsTTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000517485.6:c.*130_*133delinsTTCA (RAD21) ENSP00000427923.2:n.*130_*133delinsTTCA
ENST00000517749.2:c.*130_*133delinsTTCA (RAD21) ENSP00000430273.2:n.*130_*133delinsTTCA
ENST00000519837.6:c.*130_*133delinsTTCA (RAD21) ENSP00000430524.2:n.*130_*133delinsTTCA
ENST00000520992.6:c.*130_*133delinsTTCA (RAD21) ENSP00000429342.2:n.*130_*133delinsTTCA
ENST00000522699.2:c.*130_*133delinsTTCA (RAD21) ENSP00000428158.2:n.*130_*133delinsTTCA
ENST00000523986.6:n.4995_4998delinsTTCA (RAD21)
ENST00000685972.1:n.5329_5332delinsTTCA (RAD21)
ENST00000687122.1:n.4854_4857delinsTTCA (RAD21)
ENST00000687358.1:c.*130_*133delinsTTCA (RAD21) ENSP00000509687.1:n.*130_*133delinsTTCA
ENST00000687902.1:c.*401_*404delinsTTCA (RAD21) ENSP00000510729.1:n.*401_*404delinsTTCA
ENST00000689124.1:n.2240_2243delinsTTCA (RAD21)
ENST00000689154.1:n.1918_1921delinsTTCA (RAD21)
ENST00000690166.1:n.6895_6898delinsTTCA (RAD21)
ENST00000297338.7:c.*130_*133delinsTTCA (RAD21) MANE Select ENSP00000297338.2:n.*130_*133delinsTTCA
ENST00000297338.6:c.*130_*133delinsTTCA (RAD21) ENSP00000297338.2:n.*130_*133delinsTTCA
ENST00000517749.1:c.*130_*133delinsTTCA (RAD21) ENSP00000430273.1:n.*130_*133delinsTTCA
ENST00000517820.1:c.189-1521_189-1518delinsTGAA (UTP23) ENSP00000427767.1:n.189-1521_189-1518delinsTGAA
ENST00000518055.1:c.*130_*133delinsTTCA (RAD21) ENSP00000428003.1:n.*130_*133delinsTTCA
ENST00000520733.5:c.46-1521_46-1518delinsTGAA (UTP23) ENSP00000429384.1:n.46-1521_46-1518delinsTGAA
ENST00000521703.5:c.*93-1521_*93-1518delinsTGAA (UTP23) ENSP00000428455.1:n.*93-1521_*93-1518delinsTGAA
ENST00000523986.5:c.*130_*133delinsTTCA (RAD21) ENSP00000428513.1:n.*130_*133delinsTTCA
ENST00000524128.1:c.*93-1521_*93-1518delinsTGAA (UTP23) ENSP00000430309.1:n.*93-1521_*93-1518delinsTGAA
NM_006265.2:c.*130_*133delinsTTCA , LRG_772t1:c.*130_*133delinsTTCA (RAD21) NP_006256.1:n.*130_*133delinsTTCA
XR_928356.1:n.663-1521_663-1518delinsTGAA (UTP23)
NM_006265.3:c.*130_*133delinsTTCA (RAD21) MANE Select NP_006256.1:n.*130_*133delinsTTCA