Canonical Allele Identifier: CA2768437702
Gene: RAD50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132591875_132591877del , CM000667.2:g.132591875_132591877del GRCh38
NC_000005.9:g.131927567_131927569del , CM000667.1:g.131927567_131927569del GRCh37
NC_000005.8:g.131955466_131955468del NCBI36
NG_021151.1:g.39952_39954del
NG_021151.2:g.39899_39901del

Transcript Alleles

HGVS Amino-acid change
ENST00000378823.8:c.1636-2_1636del
ENST00000638452.2:c.1339-2_1339del
ENST00000638504.1:n.1322-2_1322del
ENST00000638568.2:c.1339-2_1339del
ENST00000639899.1:n.2155-2_2155del
ENST00000640655.2:c.1339-2_1339del
ENST00000651160.1:c.1636-2_1636del
ENST00000651541.1:c.1339-2_1339del
ENST00000651658.1:n.2063-2_2063del
ENST00000651723.1:c.*1719-2_*1719del
ENST00000652016.1:c.1636-2_1636del
ENST00000652485.1:c.1669-2_1669del
ENST00000378823.7:c.1636-2_1636del
ENST00000423956.5:c.1635+469_1635+471del ENSP00000390971.1:n.1635+469_1635+471del
ENST00000434288.1:c.131-2_131del
ENST00000453394.5:c.1453-2_1453del
ENST00000533482.5:c.*1262-2_*1262del
NM_005732.3:c.1636-2_1636del
NM_005732.4:c.1636-2_1636del