Canonical Allele Identifier: CA2578402651
Gene: RAD50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132591851_132591852del , CM000667.2:g.132591851_132591852del GRCh38
NC_000005.9:g.131927543_131927544del , CM000667.1:g.131927543_131927544del GRCh37
NC_000005.8:g.131955442_131955443del NCBI36
NG_021151.1:g.39928_39929del
NG_021151.2:g.39875_39876del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378823.8:c.1636-26_1636-25del MANE Select ENSP00000368100.4:n.1636-26_1636-25del
ENST00000638452.2:c.1339-26_1339-25del ENSP00000492349.2:n.1339-26_1339-25del
ENST00000638504.1:n.1322-26_1322-25del
ENST00000638568.2:c.1339-26_1339-25del ENSP00000491158.2:n.1339-26_1339-25del
ENST00000639899.1:n.2155-26_2155-25del
ENST00000640655.2:c.1339-26_1339-25del ENSP00000491596.2:n.1339-26_1339-25del
ENST00000651160.1:c.1636-26_1636-25del ENSP00000498829.1:n.1636-26_1636-25del
ENST00000651541.1:c.1339-26_1339-25del ENSP00000498795.1:n.1339-26_1339-25del
ENST00000651658.1:n.2063-26_2063-25del
ENST00000651723.1:c.*1719-26_*1719-25del ENSP00000498237.1:n.*1719-26_*1719-25del
ENST00000652016.1:c.1636-26_1636-25del ENSP00000498267.1:n.1636-26_1636-25del
ENST00000652485.1:c.1669-26_1669-25del ENSP00000498973.1:n.1669-26_1669-25del
ENST00000378823.7:c.1636-26_1636-25del ENSP00000368100.4:n.1636-26_1636-25del
ENST00000423956.5:c.1635+445_1635+446del ENSP00000390971.1:n.1635+445_1635+446del
ENST00000434288.1:c.131-26_131-25del
ENST00000453394.5:c.1453-26_1453-25del ENSP00000400049.1:n.1453-26_1453-25del
ENST00000533482.5:c.*1262-26_*1262-25del ENSP00000431225.1:n.*1262-26_*1262-25del
NM_005732.3:c.1636-26_1636-25del NP_005723.2:n.1636-26_1636-25del
NM_005732.4:c.1636-26_1636-25del MANE Select NP_005723.2:n.1636-26_1636-25del