Canonical Allele Identifier: CA190551

Gene: RAD50

Linked Data

• ClinVar Variation Id: 184945
• ClinVar RCV Id: RCV000164289
• dbSNP Id: rs769473693
• ExAC: 5:131925471 A / G
• gnomAD v2: 5-131925471-A-G
• gnomAD v4: 5-132589779-A-G
• MyVariant Identifiers: chr5:g.131925471A>G (hg19) ; chr5:g.132589779A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132589779A>G , CM000667.2:g.132589779A>G	GRCh38
NC_000005.9:g.131925471A>G , CM000667.1:g.131925471A>G	GRCh37
NC_000005.8:g.131953370A>G	NCBI36
NG_021151.1:g.37856A>G
NG_021151.2:g.37803A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1394A>G MANE Select	ENSP00000368100.4:p.Gln465Arg
ENST00000638452.2:c.1097A>G	ENSP00000492349.2:p.Gln366Arg
ENST00000638504.1:n.1080A>G
ENST00000638568.2:c.1097A>G	ENSP00000491158.2:p.Gln366Arg
ENST00000639899.1:n.1913A>G
ENST00000640655.2:c.1097A>G	ENSP00000491596.2:p.Gln366Arg
ENST00000651160.1:c.1394A>G	ENSP00000498829.1:p.Gln465Arg
ENST00000651541.1:c.1097A>G	ENSP00000498795.1:p.Gln366Arg
ENST00000651658.1:n.1821A>G
ENST00000651723.1:c.*1477A>G	ENSP00000498237.1:n.*1477A>G
ENST00000652016.1:c.1394A>G	ENSP00000498267.1:p.Gln465Arg
ENST00000652485.1:c.1394A>G	ENSP00000498973.1:p.Gln465Arg
ENST00000378823.7:c.1394A>G	ENSP00000368100.4:p.Gln465Arg
ENST00000423956.5:c.1394A>G	ENSP00000390971.1:p.Gln465Arg
ENST00000453394.5:c.1394A>G	ENSP00000400049.1:p.Gln465Arg
ENST00000533482.5:c.*1020A>G	ENSP00000431225.1:n.*1020A>G
NM_005732.3:c.1394A>G	NP_005723.2:p.Gln465Arg
NM_005732.4:c.1394A>G MANE Select	NP_005723.2:p.Gln465Arg