Canonical Allele Identifier: CA1583229573

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132609174_132609179delinsAATTAT , CM000667.2:g.132609174_132609179delinsAATTAT	GRCh38
NC_000005.9:g.131944866_131944871delinsAATTAT , CM000667.1:g.131944866_131944871delinsAATTAT	GRCh37
NC_000005.8:g.131972765_131972770delinsAATTAT	NCBI36
NG_021151.1:g.57251_57256delinsAATTAT
NG_021151.2:g.57198_57203delinsAATTAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.2887_2892delinsAATTAT MANE Select	ENSP00000368100.4:p.Asn963=
ENST00000638452.2:c.2590_2595delinsAATTAT	ENSP00000492349.2:p.Asn864=
ENST00000638504.1:n.2495_2500delinsAATTAT
ENST00000638568.2:c.2590_2595delinsAATTAT	ENSP00000491158.2:p.Asn864=
ENST00000639899.1:n.3406_3411delinsAATTAT
ENST00000640655.2:c.2590_2595delinsAATTAT	ENSP00000491596.2:p.Asn864=
ENST00000651160.1:c.*1031_*1036delinsAATTAT	ENSP00000498829.1:n.*1031_*1036delinsAATTAT
ENST00000651723.1:c.*2970_*2975delinsAATTAT	ENSP00000498237.1:n.*2970_*2975delinsAATTAT
ENST00000378823.7:c.2887_2892delinsAATTAT	ENSP00000368100.4:p.Asn963=
ENST00000423956.5:c.*1073_*1078delinsAATTAT	ENSP00000390971.1:n.*1073_*1078delinsAATTAT
ENST00000533482.5:c.*2513_*2518delinsAATTAT	ENSP00000431225.1:n.*2513_*2518delinsAATTAT
NM_005732.3:c.2887_2892delinsAATTAT	NP_005723.2:p.Asn963=
NM_005732.4:c.2887_2892delinsAATTAT MANE Select	NP_005723.2:p.Asn963=