Canonical Allele Identifier: CA645541926
Gene: RAD50 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132589693_132589697del , CM000667.2:g.132589693_132589697del GRCh38
NC_000005.9:g.131925385_131925389del , CM000667.1:g.131925385_131925389del GRCh37
NC_000005.8:g.131953284_131953288del NCBI36
NG_021151.1:g.37770_37774del
NG_021151.2:g.37717_37721del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378823.8:c.1308_1312del MANE Select ENSP00000368100.4:p.Leu439LysfsTer4
ENST00000638452.2:c.1011_1015del ENSP00000492349.2:p.Leu340LysfsTer4
ENST00000638504.1:n.994_998del
ENST00000638568.2:c.1011_1015del ENSP00000491158.2:p.Leu340LysfsTer4
ENST00000639899.1:n.1827_1831del
ENST00000640655.2:c.1011_1015del ENSP00000491596.2:p.Leu340LysfsTer4
ENST00000651160.1:c.1308_1312del ENSP00000498829.1:p.Leu439LysfsTer4
ENST00000651541.1:c.1011_1015del ENSP00000498795.1:p.Leu340LysfsTer4
ENST00000651658.1:n.1735_1739del
ENST00000651723.1:c.*1391_*1395del ENSP00000498237.1:n.*1391_*1395del
ENST00000652016.1:c.1308_1312del ENSP00000498267.1:p.Leu439LysfsTer4
ENST00000652485.1:c.1308_1312del ENSP00000498973.1:p.Leu439LysfsTer4
ENST00000378823.7:c.1308_1312del ENSP00000368100.4:p.Leu439LysfsTer4
ENST00000423956.5:c.1308_1312del ENSP00000390971.1:p.Leu439LysfsTer4
ENST00000453394.5:c.1308_1312del ENSP00000400049.1:p.Leu439LysfsTer4
ENST00000533482.5:c.*934_*938del ENSP00000431225.1:n.*934_*938del
NM_005732.3:c.1308_1312del NP_005723.2:p.Leu439LysfsTer4
NM_005732.4:c.1308_1312del MANE Select NP_005723.2:p.Leu439LysfsTer4