Canonical Allele Identifier: CA360943910
Gene: RAD50 HGNC NCBI

Linked Data

ClinVar Variation Id: 938723
ClinVar RCV Id: RCV001207998
dbSNP Id: rs1750663361

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132589712A>G , CM000667.2:g.132589712A>G GRCh38
NC_000005.9:g.131925404A>G , CM000667.1:g.131925404A>G GRCh37
NC_000005.8:g.131953303A>G NCBI36
NG_021151.1:g.37789A>G
NG_021151.2:g.37736A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378823.8:c.1327A>G MANE Select ENSP00000368100.4:p.Ile443Val
ENST00000638452.2:c.1030A>G ENSP00000492349.2:p.Ile344Val
ENST00000638504.1:n.1013A>G
ENST00000638568.2:c.1030A>G ENSP00000491158.2:p.Ile344Val
ENST00000639899.1:n.1846A>G
ENST00000640655.2:c.1030A>G ENSP00000491596.2:p.Ile344Val
ENST00000651160.1:c.1327A>G ENSP00000498829.1:p.Ile443Val
ENST00000651541.1:c.1030A>G ENSP00000498795.1:p.Ile344Val
ENST00000651658.1:n.1754A>G
ENST00000651723.1:c.*1410A>G ENSP00000498237.1:n.*1410A>G
ENST00000652016.1:c.1327A>G ENSP00000498267.1:p.Ile443Val
ENST00000652485.1:c.1327A>G ENSP00000498973.1:p.Ile443Val
ENST00000378823.7:c.1327A>G ENSP00000368100.4:p.Ile443Val
ENST00000423956.5:c.1327A>G ENSP00000390971.1:p.Ile443Val
ENST00000453394.5:c.1327A>G ENSP00000400049.1:p.Ile443Val
ENST00000533482.5:c.*953A>G ENSP00000431225.1:n.*953A>G
NM_005732.3:c.1327A>G NP_005723.2:p.Ile443Val
NM_005732.4:c.1327A>G MANE Select NP_005723.2:p.Ile443Val