Canonical Allele Identifier: CA1583233401
Gene: RAD50 HGNC NCBI

Linked Data

dbSNP Id: rs1751205916

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132617988del , CM000667.2:g.132617988del GRCh38
NC_000005.9:g.131953680del , CM000667.1:g.131953680del GRCh37
NC_000005.8:g.131981579del NCBI36
NG_021151.1:g.66065del
NG_021151.2:g.66012del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378823.8:c.3165-82del MANE Select ENSP00000368100.4:n.3165-82del
ENST00000638452.2:c.2868-82del ENSP00000492349.2:n.2868-82del
ENST00000638504.1:n.2773-82del
ENST00000638568.2:c.2868-82del ENSP00000491158.2:n.2868-82del
ENST00000639899.1:n.3684-82del
ENST00000640655.2:c.2868-82del ENSP00000491596.2:n.2868-82del
ENST00000378823.7:c.3165-82del ENSP00000368100.4:n.3165-82del
ENST00000533482.5:c.*2791-82del ENSP00000431225.1:n.*2791-82del
NM_005732.3:c.3165-82del NP_005723.2:n.3165-82del
NM_005732.4:c.3165-82del MANE Select NP_005723.2:n.3165-82del