Canonical Allele Identifier: CA2710356261

Gene: RAD50

Linked Data

• dbSNP Id: rs2149840997

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132588681_132588682insCTT , CM000667.2:g.132588681_132588682insCTT	GRCh38
NC_000005.9:g.131924373_131924374insCTT , CM000667.1:g.131924373_131924374insCTT	GRCh37
NC_000005.8:g.131952272_131952273insCTT	NCBI36
NG_021151.1:g.36758_36759insCTT
NG_021151.2:g.36705_36706insCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1052-6_1052-5insCTT MANE Select	ENSP00000368100.4:n.1052-6_1052-5insCTT
ENST00000638452.2:c.755-6_755-5insCTT	ENSP00000492349.2:n.755-6_755-5insCTT
ENST00000638504.1:n.738-6_738-5insCTT
ENST00000638568.2:c.755-6_755-5insCTT	ENSP00000491158.2:n.755-6_755-5insCTT
ENST00000639899.1:n.1571-6_1571-5insCTT
ENST00000640655.2:c.755-6_755-5insCTT	ENSP00000491596.2:n.755-6_755-5insCTT
ENST00000651160.1:c.1052-6_1052-5insCTT	ENSP00000498829.1:n.1052-6_1052-5insCTT
ENST00000651541.1:c.755-6_755-5insCTT	ENSP00000498795.1:n.755-6_755-5insCTT
ENST00000651658.1:n.1479-6_1479-5insCTT
ENST00000651723.1:c.*1135-6_*1135-5insCTT	ENSP00000498237.1:n.*1135-6_*1135-5insCTT
ENST00000652016.1:c.1052-6_1052-5insCTT	ENSP00000498267.1:n.1052-6_1052-5insCTT
ENST00000652485.1:c.1052-6_1052-5insCTT	ENSP00000498973.1:n.1052-6_1052-5insCTT
ENST00000378823.7:c.1052-6_1052-5insCTT	ENSP00000368100.4:n.1052-6_1052-5insCTT
ENST00000423956.5:c.1052-6_1052-5insCTT	ENSP00000390971.1:n.1052-6_1052-5insCTT
ENST00000453394.5:c.1052-6_1052-5insCTT	ENSP00000400049.1:n.1052-6_1052-5insCTT
ENST00000487596.1:n.618-6_618-5insCTT
ENST00000533482.5:c.*678-6_*678-5insCTT	ENSP00000431225.1:n.*678-6_*678-5insCTT
NM_005732.3:c.1052-6_1052-5insCTT	NP_005723.2:n.1052-6_1052-5insCTT
NM_005732.4:c.1052-6_1052-5insCTT MANE Select	NP_005723.2:n.1052-6_1052-5insCTT