Canonical Allele Identifier: CA1583216702
Gene: RAD50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132556968_132556970delinsTAG , CM000667.2:g.132556968_132556970delinsTAG GRCh38
NC_000005.9:g.131892660_131892662delinsTAG , CM000667.1:g.131892660_131892662delinsTAG GRCh37
NC_000005.8:g.131920559_131920561delinsTAG NCBI36
NG_021151.1:g.5045_5047delinsTAG
NG_021151.2:g.4992_4994delinsTAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000638452.2:c.-168-2316_-168-2314delinsTAG ENSP00000492349.2:n.-168-2316_-168-2314delinsTAG
ENST00000638504.1:n.207-2316_207-2314delinsTAG
ENST00000638568.2:c.-169+495_-169+497delinsTAG ENSP00000491158.2:n.-169+495_-169+497delinsTAG
ENST00000639899.1:n.290-2316_290-2314delinsTAG
ENST00000640655.2:c.-168-2316_-168-2314delinsTAG ENSP00000491596.2:n.-168-2316_-168-2314delinsTAG
ENST00000651541.1:c.-210_-208delinsTAG ENSP00000498795.1:n.-210_-208delinsTAG
ENST00000378823.7:c.-357_-355delinsTAG ENSP00000368100.4:n.-357_-355delinsTAG
ENST00000416135.5:c.-169+495_-169+497delinsTAG ENSP00000389515.1:n.-169+495_-169+497delinsTAG
ENST00000533482.5:c.-357_-355delinsTAG ENSP00000431225.1:n.-357_-355delinsTAG
NM_005732.3:c.-357_-355delinsTAG NP_005723.2:n.-357_-355delinsTAG