Canonical Allele Identifier: CA2710355896
Gene: RAD50 HGNC NCBI

Linked Data

dbSNP Id: rs2149840967

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132588654_132588655del , CM000667.2:g.132588654_132588655del GRCh38
NC_000005.9:g.131924346_131924347del , CM000667.1:g.131924346_131924347del GRCh37
NC_000005.8:g.131952245_131952246del NCBI36
NG_021151.1:g.36731_36732del
NG_021151.2:g.36678_36679del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378823.8:c.1052-33_1052-32del MANE Select ENSP00000368100.4:n.1052-33_1052-32del
ENST00000638452.2:c.755-33_755-32del ENSP00000492349.2:n.755-33_755-32del
ENST00000638504.1:n.738-33_738-32del
ENST00000638568.2:c.755-33_755-32del ENSP00000491158.2:n.755-33_755-32del
ENST00000639899.1:n.1571-33_1571-32del
ENST00000640655.2:c.755-33_755-32del ENSP00000491596.2:n.755-33_755-32del
ENST00000651160.1:c.1052-33_1052-32del ENSP00000498829.1:n.1052-33_1052-32del
ENST00000651541.1:c.755-33_755-32del ENSP00000498795.1:n.755-33_755-32del
ENST00000651658.1:n.1479-33_1479-32del
ENST00000651723.1:c.*1135-33_*1135-32del ENSP00000498237.1:n.*1135-33_*1135-32del
ENST00000652016.1:c.1052-33_1052-32del ENSP00000498267.1:n.1052-33_1052-32del
ENST00000652485.1:c.1052-33_1052-32del ENSP00000498973.1:n.1052-33_1052-32del
ENST00000378823.7:c.1052-33_1052-32del ENSP00000368100.4:n.1052-33_1052-32del
ENST00000423956.5:c.1052-33_1052-32del ENSP00000390971.1:n.1052-33_1052-32del
ENST00000453394.5:c.1052-33_1052-32del ENSP00000400049.1:n.1052-33_1052-32del
ENST00000487596.1:n.618-33_618-32del
ENST00000533482.5:c.*678-33_*678-32del ENSP00000431225.1:n.*678-33_*678-32del
NM_005732.3:c.1052-33_1052-32del NP_005723.2:n.1052-33_1052-32del
NM_005732.4:c.1052-33_1052-32del MANE Select NP_005723.2:n.1052-33_1052-32del