Canonical Allele Identifier: CA1583246321

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132604920_132604922delinsATT , CM000667.2:g.132604920_132604922delinsATT	GRCh38
NC_000005.9:g.131940612_131940614delinsATT , CM000667.1:g.131940612_131940614delinsATT	GRCh37
NC_000005.8:g.131968511_131968513delinsATT	NCBI36
NG_021151.1:g.52997_52999delinsATT
NG_021151.2:g.52944_52946delinsATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.2639_2641delinsATT MANE Select	ENSP00000368100.4:p.Asn880=
ENST00000638452.2:c.2342_2344delinsATT	ENSP00000492349.2:p.Asn781=
ENST00000638504.1:n.2247_2249delinsATT
ENST00000638568.2:c.2342_2344delinsATT	ENSP00000491158.2:p.Asn781=
ENST00000639899.1:n.3158_3160delinsATT
ENST00000640655.2:c.2342_2344delinsATT	ENSP00000491596.2:p.Asn781=
ENST00000651160.1:c.*783_*785delinsATT	ENSP00000498829.1:n.*783_*785delinsATT
ENST00000651723.1:c.*2722_*2724delinsATT	ENSP00000498237.1:n.*2722_*2724delinsATT
ENST00000652016.1:c.*856_*858delinsATT	ENSP00000498267.1:n.*856_*858delinsATT
ENST00000652485.1:c.2672_2674delinsATT	ENSP00000498973.1:p.Asn891=
ENST00000378823.7:c.2639_2641delinsATT	ENSP00000368100.4:p.Asn880=
ENST00000423956.5:c.*825_*827delinsATT	ENSP00000390971.1:n.*825_*827delinsATT
ENST00000533482.5:c.*2265_*2267delinsATT	ENSP00000431225.1:n.*2265_*2267delinsATT
NM_005732.3:c.2639_2641delinsATT	NP_005723.2:p.Asn880=
NM_005732.4:c.2639_2641delinsATT MANE Select	NP_005723.2:p.Asn880=