Canonical Allele Identifier: CA2675217665

Gene: RAD50

Linked Data

• gnomAD v4: 5-132591805-AATTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132591810_132591813del , CM000667.2:g.132591810_132591813del	GRCh38
NC_000005.9:g.131927502_131927505del , CM000667.1:g.131927502_131927505del	GRCh37
NC_000005.8:g.131955401_131955404del	NCBI36
NG_021151.1:g.39887_39890del
NG_021151.2:g.39834_39837del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1636-67_1636-64del MANE Select	ENSP00000368100.4:n.1636-67_1636-64del
ENST00000638452.2:c.1339-67_1339-64del	ENSP00000492349.2:n.1339-67_1339-64del
ENST00000638504.1:n.1322-67_1322-64del
ENST00000638568.2:c.1339-67_1339-64del	ENSP00000491158.2:n.1339-67_1339-64del
ENST00000639899.1:n.2155-67_2155-64del
ENST00000640655.2:c.1339-67_1339-64del	ENSP00000491596.2:n.1339-67_1339-64del
ENST00000651160.1:c.1636-67_1636-64del	ENSP00000498829.1:n.1636-67_1636-64del
ENST00000651541.1:c.1339-67_1339-64del	ENSP00000498795.1:n.1339-67_1339-64del
ENST00000651658.1:n.2063-67_2063-64del
ENST00000651723.1:c.*1719-67_*1719-64del	ENSP00000498237.1:n.*1719-67_*1719-64del
ENST00000652016.1:c.1636-67_1636-64del	ENSP00000498267.1:n.1636-67_1636-64del
ENST00000652485.1:c.1669-67_1669-64del	ENSP00000498973.1:n.1669-67_1669-64del
ENST00000378823.7:c.1636-67_1636-64del	ENSP00000368100.4:n.1636-67_1636-64del
ENST00000423956.5:c.1635+404_1635+407del	ENSP00000390971.1:n.1635+404_1635+407del
ENST00000434288.1:c.131-67_131-64del
ENST00000453394.5:c.1453-67_1453-64del	ENSP00000400049.1:n.1453-67_1453-64del
ENST00000533482.5:c.*1262-67_*1262-64del	ENSP00000431225.1:n.*1262-67_*1262-64del
NM_005732.3:c.1636-67_1636-64del	NP_005723.2:n.1636-67_1636-64del
NM_005732.4:c.1636-67_1636-64del MANE Select	NP_005723.2:n.1636-67_1636-64del