Canonical Allele Identifier: CA2768437036
Gene: RAD50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132575993_132576028del , CM000667.2:g.132575993_132576028del GRCh38
NC_000005.9:g.131911685_131911720del , CM000667.1:g.131911685_131911720del GRCh37
NC_000005.8:g.131939584_131939619del NCBI36
NG_021151.1:g.24070_24105del
NG_021151.2:g.24017_24052del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378823.8:c.365+65_365+100del MANE Select ENSP00000368100.4:n.365+65_365+100del
ENST00000638452.2:c.68+65_68+100del ENSP00000492349.2:n.68+65_68+100del
ENST00000638504.1:n.442+65_442+100del
ENST00000638568.2:c.68+65_68+100del ENSP00000491158.2:n.68+65_68+100del
ENST00000639899.1:n.525+65_525+100del
ENST00000640655.2:c.68+65_68+100del ENSP00000491596.2:n.68+65_68+100del
ENST00000651160.1:c.365+65_365+100del ENSP00000498829.1:n.365+65_365+100del
ENST00000651541.1:c.68+65_68+100del ENSP00000498795.1:n.68+65_68+100del
ENST00000651658.1:n.433+65_433+100del
ENST00000651723.1:c.*448+130_*448+165del ENSP00000498237.1:n.*448+130_*448+165del
ENST00000652016.1:c.365+65_365+100del ENSP00000498267.1:n.365+65_365+100del
ENST00000652485.1:c.365+65_365+100del ENSP00000498973.1:n.365+65_365+100del
ENST00000378823.7:c.365+65_365+100del ENSP00000368100.4:n.365+65_365+100del
ENST00000416135.5:c.68+65_68+100del ENSP00000389515.1:n.68+65_68+100del
ENST00000423956.5:c.365+65_365+100del ENSP00000390971.1:n.365+65_365+100del
ENST00000453394.5:c.365+65_365+100del ENSP00000400049.1:n.365+65_365+100del
ENST00000533482.5:c.300+130_300+165del ENSP00000431225.1:n.300+130_300+165del
NM_005732.3:c.365+65_365+100del NP_005723.2:n.365+65_365+100del
NM_005732.4:c.365+65_365+100del MANE Select NP_005723.2:n.365+65_365+100del