Canonical Allele Identifier: CA1583254244
Gene: RAD50 HGNC NCBI
TH2LCRR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132641386_132641387delinsCA , CM000667.2:g.132641386_132641387delinsCA GRCh38
NC_000005.9:g.131977078_131977079delinsCA , CM000667.1:g.131977078_131977079delinsCA GRCh37
NC_000005.8:g.132004977_132004978delinsCA NCBI36
NG_021151.1:g.89463_89464delinsCA
NG_021151.2:g.89410_89411delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000378823.8:c.3752+581_3752+582delinsCA (RAD50) MANE Select ENSP00000368100.4:n.3752+581_3752+582delinsCA
ENST00000638452.2:c.3455+581_3455+582delinsCA ENSP00000492349.2:n.3455+581_3455+582delinsCA
ENST00000638504.1:n.3360+581_3360+582delinsCA
ENST00000638568.2:c.3455+581_3455+582delinsCA ENSP00000491158.2:n.3455+581_3455+582delinsCA
ENST00000639899.1:n.4271+581_4271+582delinsCA
ENST00000640655.2:c.3455+581_3455+582delinsCA ENSP00000491596.2:n.3455+581_3455+582delinsCA
ENST00000651249.1:c.588+581_588+582delinsCA (RAD50)
ENST00000378823.7:c.3752+581_3752+582delinsCA (RAD50) ENSP00000368100.4:n.3752+581_3752+582delinsCA
ENST00000455677.1:c.387+581_387+582delinsCA (RAD50)
ENST00000533482.5:c.*3378+581_*3378+582delinsCA (RAD50) ENSP00000431225.1:n.*3378+581_*3378+582delinsCA
NM_005732.3:c.3752+581_3752+582delinsCA (RAD50) NP_005723.2:n.3752+581_3752+582delinsCA
NR_132124.1:n.45+359_45+360delinsTG (TH2LCRR)
NR_132125.1:n.189+811_189+812delinsTG (TH2LCRR)
NR_132126.1:n.175-3122_175-3121delinsTG (TH2LCRR)
XR_427771.1:n.426+359_426+360delinsTG (TH2LCRR)
NM_005732.4:c.3752+581_3752+582delinsCA (RAD50) MANE Select NP_005723.2:n.3752+581_3752+582delinsCA