Canonical Allele Identifier: CA1583239729
Gene: RAD50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132589929_132589940delinsAATAAAAACATC , CM000667.2:g.132589929_132589940delinsAATAAAAACATC GRCh38
NC_000005.9:g.131925621_131925632delinsAATAAAAACATC , CM000667.1:g.131925621_131925632delinsAATAAAAACATC GRCh37
NC_000005.8:g.131953520_131953531delinsAATAAAAACATC NCBI36
NG_021151.1:g.38006_38017delinsAATAAAAACATC
NG_021151.2:g.37953_37964delinsAATAAAAACATC

Transcript Alleles

HGVS Amino-acid Change
ENST00000378823.8:c.1452+92_1452+103delinsAATAAAAACATC MANE Select ENSP00000368100.4:n.1452+92_1452+103delinsAATAAAAACATC
ENST00000638452.2:c.1155+92_1155+103delinsAATAAAAACATC ENSP00000492349.2:n.1155+92_1155+103delinsAATAAAAACATC
ENST00000638504.1:n.1138+92_1138+103delinsAATAAAAACATC
ENST00000638568.2:c.1155+92_1155+103delinsAATAAAAACATC ENSP00000491158.2:n.1155+92_1155+103delinsAATAAAAACATC
ENST00000639899.1:n.1971+92_1971+103delinsAATAAAAACATC
ENST00000640655.2:c.1155+92_1155+103delinsAATAAAAACATC ENSP00000491596.2:n.1155+92_1155+103delinsAATAAAAACATC
ENST00000651160.1:c.1452+92_1452+103delinsAATAAAAACATC ENSP00000498829.1:n.1452+92_1452+103delinsAATAAAAACATC
ENST00000651541.1:c.1155+92_1155+103delinsAATAAAAACATC ENSP00000498795.1:n.1155+92_1155+103delinsAATAAAAACATC
ENST00000651658.1:n.1879+92_1879+103delinsAATAAAAACATC
ENST00000651723.1:c.*1535+92_*1535+103delinsAATAAAAACATC ENSP00000498237.1:n.*1535+92_*1535+103delinsAATAAAAACATC
ENST00000652016.1:c.1452+92_1452+103delinsAATAAAAACATC ENSP00000498267.1:n.1452+92_1452+103delinsAATAAAAACATC
ENST00000652485.1:c.1452+92_1452+103delinsAATAAAAACATC ENSP00000498973.1:n.1452+92_1452+103delinsAATAAAAACATC
ENST00000378823.7:c.1452+92_1452+103delinsAATAAAAACATC ENSP00000368100.4:n.1452+92_1452+103delinsAATAAAAACATC
ENST00000423956.5:c.1452+92_1452+103delinsAATAAAAACATC ENSP00000390971.1:n.1452+92_1452+103delinsAATAAAAACATC
ENST00000453394.5:c.1452+92_1452+103delinsAATAAAAACATC ENSP00000400049.1:n.1452+92_1452+103delinsAATAAAAACATC
ENST00000533482.5:c.*1078+92_*1078+103delinsAATAAAAACATC ENSP00000431225.1:n.*1078+92_*1078+103delinsAATAAAAACATC
NM_005732.3:c.1452+92_1452+103delinsAATAAAAACATC NP_005723.2:n.1452+92_1452+103delinsAATAAAAACATC
NM_005732.4:c.1452+92_1452+103delinsAATAAAAACATC MANE Select NP_005723.2:n.1452+92_1452+103delinsAATAAAAACATC