Canonical Allele Identifier: CA2533213901
Gene: RAD50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132618457C>A , CM000667.2:g.132618457C>A GRCh38
NC_000005.9:g.131954149C>A , CM000667.1:g.131954149C>A GRCh37
NC_000005.8:g.131982048C>A NCBI36
NG_021151.1:g.66534C>A
NG_021151.2:g.66481C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378823.8:c.3389+163C>A MANE Select ENSP00000368100.4:n.3389+163C>A
ENST00000638452.2:c.3092+163C>A ENSP00000492349.2:n.3092+163C>A
ENST00000638504.1:n.2997+163C>A
ENST00000638568.2:c.3092+163C>A ENSP00000491158.2:n.3092+163C>A
ENST00000639899.1:n.3908+163C>A
ENST00000640655.2:c.3092+163C>A ENSP00000491596.2:n.3092+163C>A
ENST00000651249.1:c.225+163C>A
ENST00000378823.7:c.3389+163C>A ENSP00000368100.4:n.3389+163C>A
ENST00000455677.1:c.24+163C>A
ENST00000533482.5:c.*3015+163C>A ENSP00000431225.1:n.*3015+163C>A
NM_005732.3:c.3389+163C>A NP_005723.2:n.3389+163C>A
NM_005732.4:c.3389+163C>A MANE Select NP_005723.2:n.3389+163C>A