Canonical Allele Identifier: CA917584269
Gene: RAD50 HGNC NCBI

Linked Data

dbSNP Id: rs1580986841

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132579057_132579059del , CM000667.2:g.132579057_132579059del GRCh38
NC_000005.9:g.131914749_131914751del , CM000667.1:g.131914749_131914751del GRCh37
NC_000005.8:g.131942648_131942650del NCBI36
NG_021151.1:g.27134_27136del
NG_021151.2:g.27081_27083del

Transcript Alleles

HGVS Amino-acid change
ENST00000378823.8:c.366-260_366-258del MANE Select ENSP00000368100.4:n.366-260_366-258del
ENST00000638452.2:c.69-260_69-258del ENSP00000492349.2:n.69-260_69-258del
ENST00000638504.1:n.442+3129_442+3131del
ENST00000638568.2:c.69-260_69-258del ENSP00000491158.2:n.69-260_69-258del
ENST00000639899.1:n.526-260_526-258del
ENST00000640655.2:c.69-260_69-258del ENSP00000491596.2:n.69-260_69-258del
ENST00000651160.1:c.366-260_366-258del ENSP00000498829.1:n.366-260_366-258del
ENST00000651541.1:c.69-260_69-258del ENSP00000498795.1:n.69-260_69-258del
ENST00000651658.1:n.434-260_434-258del
ENST00000651723.1:c.*449-260_*449-258del ENSP00000498237.1:n.*449-260_*449-258del
ENST00000652016.1:c.366-260_366-258del ENSP00000498267.1:n.366-260_366-258del
ENST00000652485.1:c.366-260_366-258del ENSP00000498973.1:n.366-260_366-258del
ENST00000378823.7:c.366-260_366-258del ENSP00000368100.4:n.366-260_366-258del
ENST00000416135.5:c.69-260_69-258del ENSP00000389515.1:n.69-260_69-258del
ENST00000423956.5:c.366-260_366-258del ENSP00000390971.1:n.366-260_366-258del
ENST00000453394.5:c.366-260_366-258del ENSP00000400049.1:n.366-260_366-258del
ENST00000533482.5:c.301-260_301-258del ENSP00000431225.1:n.301-260_301-258del
NM_005732.3:c.366-260_366-258del NP_005723.2:n.366-260_366-258del
NM_005732.4:c.366-260_366-258del MANE Select NP_005723.2:n.366-260_366-258del