Canonical Allele Identifier: CA1583217011
Gene: RAD50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132557431G= , CM000667.2:g.132557431G= GRCh38
NC_000005.9:g.131893123G= , CM000667.1:g.131893123G= GRCh37
NC_000005.8:g.131921022G= NCBI36
NG_021151.1:g.5508G=
NG_021151.2:g.5455G=

Transcript Alleles

HGVS Amino-acid change
ENST00000378823.8:c.107G= MANE Select ENSP00000368100.4:p.Gly36=
ENST00000638452.2:c.-168-1853G= ENSP00000492349.2:n.-168-1853G=
ENST00000638504.1:n.207-1853G=
ENST00000638568.2:c.-169+958G= ENSP00000491158.2:n.-169+958G=
ENST00000639899.1:n.290-1853G=
ENST00000640655.2:c.-168-1853G= ENSP00000491596.2:n.-168-1853G=
ENST00000651160.1:c.107G= ENSP00000498829.1:p.Gly36=
ENST00000651541.1:c.-169+422G= ENSP00000498795.1:n.-169+422G=
ENST00000651658.1:n.175G=
ENST00000651723.1:c.107G= ENSP00000498237.1:p.Gly36=
ENST00000652016.1:c.107G= ENSP00000498267.1:p.Gly36=
ENST00000652485.1:c.107G= ENSP00000498973.1:p.Gly36=
ENST00000378823.7:c.107G= ENSP00000368100.4:p.Gly36=
ENST00000416135.5:c.-169+958G= ENSP00000389515.1:n.-169+958G=
ENST00000423956.5:c.107G= ENSP00000390971.1:p.Gly36=
ENST00000453394.5:c.107G= ENSP00000400049.1:p.Gly36=
ENST00000533482.5:c.107G= ENSP00000431225.1:p.Gly36=
NM_005732.3:c.107G= NP_005723.2:p.Gly36=
NM_005732.4:c.107G= MANE Select NP_005723.2:p.Gly36=