Canonical Allele Identifier: CA2768437900

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132589464_132589465del , CM000667.2:g.132589464_132589465del	GRCh38
NC_000005.9:g.131925156_131925157del , CM000667.1:g.131925156_131925157del	GRCh37
NC_000005.8:g.131953055_131953056del	NCBI36
NG_021151.1:g.37541_37542del
NG_021151.2:g.37488_37489del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1246-167_1246-166del MANE Select	ENSP00000368100.4:n.1246-167_1246-166del
ENST00000638452.2:c.949-167_949-166del	ENSP00000492349.2:n.949-167_949-166del
ENST00000638504.1:n.932-167_932-166del
ENST00000638568.2:c.949-167_949-166del	ENSP00000491158.2:n.949-167_949-166del
ENST00000639899.1:n.1765-167_1765-166del
ENST00000640655.2:c.949-167_949-166del	ENSP00000491596.2:n.949-167_949-166del
ENST00000651160.1:c.1246-167_1246-166del	ENSP00000498829.1:n.1246-167_1246-166del
ENST00000651541.1:c.949-167_949-166del	ENSP00000498795.1:n.949-167_949-166del
ENST00000651658.1:n.1673-167_1673-166del
ENST00000651723.1:c.*1329-167_*1329-166del	ENSP00000498237.1:n.*1329-167_*1329-166del
ENST00000652016.1:c.1246-167_1246-166del	ENSP00000498267.1:n.1246-167_1246-166del
ENST00000652485.1:c.1246-167_1246-166del	ENSP00000498973.1:n.1246-167_1246-166del
ENST00000378823.7:c.1246-167_1246-166del	ENSP00000368100.4:n.1246-167_1246-166del
ENST00000423956.5:c.1246-167_1246-166del	ENSP00000390971.1:n.1246-167_1246-166del
ENST00000453394.5:c.1246-167_1246-166del	ENSP00000400049.1:n.1246-167_1246-166del
ENST00000533482.5:c.*872-167_*872-166del	ENSP00000431225.1:n.*872-167_*872-166del
NM_005732.3:c.1246-167_1246-166del	NP_005723.2:n.1246-167_1246-166del
NM_005732.4:c.1246-167_1246-166del MANE Select	NP_005723.2:n.1246-167_1246-166del