Canonical Allele Identifier: CA2710364457

Gene: RAD50

Linked Data

• dbSNP Id: rs2149842602

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132591866_132591867insA , CM000667.2:g.132591866_132591867insA	GRCh38
NC_000005.9:g.131927558_131927559insA , CM000667.1:g.131927558_131927559insA	GRCh37
NC_000005.8:g.131955457_131955458insA	NCBI36
NG_021151.1:g.39943_39944insA
NG_021151.2:g.39890_39891insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1636-11_1636-10insA MANE Select	ENSP00000368100.4:n.1636-11_1636-10insA
ENST00000638452.2:c.1339-11_1339-10insA	ENSP00000492349.2:n.1339-11_1339-10insA
ENST00000638504.1:n.1322-11_1322-10insA
ENST00000638568.2:c.1339-11_1339-10insA	ENSP00000491158.2:n.1339-11_1339-10insA
ENST00000639899.1:n.2155-11_2155-10insA
ENST00000640655.2:c.1339-11_1339-10insA	ENSP00000491596.2:n.1339-11_1339-10insA
ENST00000651160.1:c.1636-11_1636-10insA	ENSP00000498829.1:n.1636-11_1636-10insA
ENST00000651541.1:c.1339-11_1339-10insA	ENSP00000498795.1:n.1339-11_1339-10insA
ENST00000651658.1:n.2063-11_2063-10insA
ENST00000651723.1:c.*1719-11_*1719-10insA	ENSP00000498237.1:n.*1719-11_*1719-10insA
ENST00000652016.1:c.1636-11_1636-10insA	ENSP00000498267.1:n.1636-11_1636-10insA
ENST00000652485.1:c.1669-11_1669-10insA	ENSP00000498973.1:n.1669-11_1669-10insA
ENST00000378823.7:c.1636-11_1636-10insA	ENSP00000368100.4:n.1636-11_1636-10insA
ENST00000423956.5:c.1635+460_1635+461insA	ENSP00000390971.1:n.1635+460_1635+461insA
ENST00000434288.1:c.131-11_131-10insA
ENST00000453394.5:c.1453-11_1453-10insA	ENSP00000400049.1:n.1453-11_1453-10insA
ENST00000533482.5:c.*1262-11_*1262-10insA	ENSP00000431225.1:n.*1262-11_*1262-10insA
NM_005732.3:c.1636-11_1636-10insA	NP_005723.2:n.1636-11_1636-10insA
NM_005732.4:c.1636-11_1636-10insA MANE Select	NP_005723.2:n.1636-11_1636-10insA