Canonical Allele Identifier: CA2841655175

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132603849del , CM000667.2:g.132603849del	GRCh38
NC_000005.9:g.131939541del , CM000667.1:g.131939541del	GRCh37
NC_000005.8:g.131967440del	NCBI36
NG_021151.1:g.51926del
NG_021151.2:g.51873del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.2398-71del MANE Select	ENSP00000368100.4:n.2398-71del
ENST00000638452.2:c.2101-71del	ENSP00000492349.2:n.2101-71del
ENST00000638504.1:n.2006-71del
ENST00000638568.2:c.2101-71del	ENSP00000491158.2:n.2101-71del
ENST00000639899.1:n.2917-71del
ENST00000640655.2:c.2101-71del	ENSP00000491596.2:n.2101-71del
ENST00000651160.1:c.*542-71del	ENSP00000498829.1:n.*542-71del
ENST00000651658.1:n.2941-71del
ENST00000651723.1:c.*2481-71del	ENSP00000498237.1:n.*2481-71del
ENST00000652016.1:c.*615-71del	ENSP00000498267.1:n.*615-71del
ENST00000652485.1:c.2431-71del	ENSP00000498973.1:n.2431-71del
ENST00000378823.7:c.2398-71del	ENSP00000368100.4:n.2398-71del
ENST00000423956.5:c.*584-71del	ENSP00000390971.1:n.*584-71del
ENST00000533482.5:c.*2024-71del	ENSP00000431225.1:n.*2024-71del
NM_005732.3:c.2398-71del	NP_005723.2:n.2398-71del
NM_005732.4:c.2398-71del MANE Select	NP_005723.2:n.2398-71del