Canonical Allele Identifier: CA2841911599

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132589840_132589843del , CM000667.2:g.132589840_132589843del	GRCh38
NC_000005.9:g.131925532_131925535del , CM000667.1:g.131925532_131925535del	GRCh37
NC_000005.8:g.131953431_131953434del	NCBI36
NG_021151.1:g.37917_37920del
NG_021151.2:g.37864_37867del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1452+3_1452+6del MANE Select	ENSP00000368100.4:n.1452+3_1452+6del
ENST00000638452.2:c.1155+3_1155+6del	ENSP00000492349.2:n.1155+3_1155+6del
ENST00000638504.1:n.1138+3_1138+6del
ENST00000638568.2:c.1155+3_1155+6del	ENSP00000491158.2:n.1155+3_1155+6del
ENST00000639899.1:n.1971+3_1971+6del
ENST00000640655.2:c.1155+3_1155+6del	ENSP00000491596.2:n.1155+3_1155+6del
ENST00000651160.1:c.1452+3_1452+6del	ENSP00000498829.1:n.1452+3_1452+6del
ENST00000651541.1:c.1155+3_1155+6del	ENSP00000498795.1:n.1155+3_1155+6del
ENST00000651658.1:n.1879+3_1879+6del
ENST00000651723.1:c.*1535+3_*1535+6del	ENSP00000498237.1:n.*1535+3_*1535+6del
ENST00000652016.1:c.1452+3_1452+6del	ENSP00000498267.1:n.1452+3_1452+6del
ENST00000652485.1:c.1452+3_1452+6del	ENSP00000498973.1:n.1452+3_1452+6del
ENST00000378823.7:c.1452+3_1452+6del	ENSP00000368100.4:n.1452+3_1452+6del
ENST00000423956.5:c.1452+3_1452+6del	ENSP00000390971.1:n.1452+3_1452+6del
ENST00000453394.5:c.1452+3_1452+6del	ENSP00000400049.1:n.1452+3_1452+6del
ENST00000533482.5:c.*1078+3_*1078+6del	ENSP00000431225.1:n.*1078+3_*1078+6del
NM_005732.3:c.1452+3_1452+6del	NP_005723.2:n.1452+3_1452+6del
NM_005732.4:c.1452+3_1452+6del MANE Select	NP_005723.2:n.1452+3_1452+6del