Canonical Allele Identifier: CA360942122

Gene: RAD50

Linked Data

• ClinVar Variation Id: 484685
• ClinVar RCV Id: RCV000568034 ; RCV003459369
• dbSNP Id: rs1184353235
• MyVariant Identifiers: chr5:g.131924403G>A (hg19) ; chr5:g.132588711G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132588711G>A , CM000667.2:g.132588711G>A	GRCh38
NC_000005.9:g.131924403G>A , CM000667.1:g.131924403G>A	GRCh37
NC_000005.8:g.131952302G>A	NCBI36
NG_021151.1:g.36788G>A
NG_021151.2:g.36735G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1076G>A MANE Select	ENSP00000368100.4:p.Arg359His
ENST00000638452.2:c.779G>A	ENSP00000492349.2:p.Arg260His
ENST00000638504.1:n.762G>A
ENST00000638568.2:c.779G>A	ENSP00000491158.2:p.Arg260His
ENST00000639899.1:n.1595G>A
ENST00000640655.2:c.779G>A	ENSP00000491596.2:p.Arg260His
ENST00000651160.1:c.1076G>A	ENSP00000498829.1:p.Arg359His
ENST00000651541.1:c.779G>A	ENSP00000498795.1:p.Arg260His
ENST00000651658.1:n.1503G>A
ENST00000651723.1:c.*1159G>A	ENSP00000498237.1:n.*1159G>A
ENST00000652016.1:c.1076G>A	ENSP00000498267.1:p.Arg359His
ENST00000652485.1:c.1076G>A	ENSP00000498973.1:p.Arg359His
ENST00000378823.7:c.1076G>A	ENSP00000368100.4:p.Arg359His
ENST00000423956.5:c.1076G>A	ENSP00000390971.1:p.Arg359His
ENST00000453394.5:c.1076G>A	ENSP00000400049.1:p.Arg359His
ENST00000487596.1:n.642G>A
ENST00000533482.5:c.*702G>A	ENSP00000431225.1:n.*702G>A
NM_005732.3:c.1076G>A	NP_005723.2:p.Arg359His
NM_005732.4:c.1076G>A MANE Select	NP_005723.2:p.Arg359His