Canonical Allele Identifier: CA1583241893

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132595061_132595064delinsATAT , CM000667.2:g.132595061_132595064delinsATAT	GRCh38
NC_000005.9:g.131930753_131930756delinsATAT , CM000667.1:g.131930753_131930756delinsATAT	GRCh37
NC_000005.8:g.131958652_131958655delinsATAT	NCBI36
NG_021151.1:g.43138_43141delinsATAT
NG_021151.2:g.43085_43088delinsATAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1969+17_1969+20delinsATAT MANE Select	ENSP00000368100.4:n.1969+17_1969+20delinsATAT
ENST00000638452.2:c.1672+17_1672+20delinsATAT	ENSP00000492349.2:n.1672+17_1672+20delinsATAT
ENST00000638504.1:n.1480-43_1480-40delinsATAT
ENST00000638568.2:c.1672+17_1672+20delinsATAT	ENSP00000491158.2:n.1672+17_1672+20delinsATAT
ENST00000639899.1:n.2488+17_2488+20delinsATAT
ENST00000640655.2:c.1672+17_1672+20delinsATAT	ENSP00000491596.2:n.1672+17_1672+20delinsATAT
ENST00000651160.1:c.*16-43_*16-40delinsATAT	ENSP00000498829.1:n.*16-43_*16-40delinsATAT
ENST00000651658.1:n.2512+17_2512+20delinsATAT
ENST00000651723.1:c.*2052+17_*2052+20delinsATAT	ENSP00000498237.1:n.*2052+17_*2052+20delinsATAT
ENST00000652016.1:c.*89-43_*89-40delinsATAT	ENSP00000498267.1:n.*89-43_*89-40delinsATAT
ENST00000652485.1:c.2002+17_2002+20delinsATAT	ENSP00000498973.1:n.2002+17_2002+20delinsATAT
ENST00000378823.7:c.1969+17_1969+20delinsATAT	ENSP00000368100.4:n.1969+17_1969+20delinsATAT
ENST00000423956.5:c.*155+17_*155+20delinsATAT	ENSP00000390971.1:n.*155+17_*155+20delinsATAT
ENST00000453394.5:c.1786+17_1786+20delinsATAT	ENSP00000400049.1:n.1786+17_1786+20delinsATAT
ENST00000533482.5:c.*1595+17_*1595+20delinsATAT	ENSP00000431225.1:n.*1595+17_*1595+20delinsATAT
NM_005732.3:c.1969+17_1969+20delinsATAT	NP_005723.2:n.1969+17_1969+20delinsATAT
NM_005732.4:c.1969+17_1969+20delinsATAT MANE Select	NP_005723.2:n.1969+17_1969+20delinsATAT