Canonical Allele Identifier: CA10578567

Gene: RAD50

Linked Data

• ClinVar Variation Id: 231374
• ClinVar RCV Id: RCV000218116
• dbSNP Id: rs876659121
• gnomAD v2: 5-131939617-A-G
• gnomAD v4: 5-132603925-A-G
• MyVariant Identifiers: chr5:g.131939617A>G (hg19) ; chr5:g.132603925A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132603925A>G , CM000667.2:g.132603925A>G	GRCh38
NC_000005.9:g.131939617A>G , CM000667.1:g.131939617A>G	GRCh37
NC_000005.8:g.131967516A>G	NCBI36
NG_021151.1:g.52002A>G
NG_021151.2:g.51949A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.2403A>G MANE Select	ENSP00000368100.4:p.Glu801=
ENST00000638452.2:c.2106A>G	ENSP00000492349.2:p.Glu702=
ENST00000638504.1:n.2011A>G
ENST00000638568.2:c.2106A>G	ENSP00000491158.2:p.Glu702=
ENST00000639899.1:n.2922A>G
ENST00000640655.2:c.2106A>G	ENSP00000491596.2:p.Glu702=
ENST00000651160.1:c.*547A>G	ENSP00000498829.1:n.*547A>G
ENST00000651658.1:n.2946A>G
ENST00000651723.1:c.*2486A>G	ENSP00000498237.1:n.*2486A>G
ENST00000652016.1:c.*620A>G	ENSP00000498267.1:n.*620A>G
ENST00000652485.1:c.2436A>G	ENSP00000498973.1:p.Glu812=
ENST00000378823.7:c.2403A>G	ENSP00000368100.4:p.Glu801=
ENST00000423956.5:c.*589A>G	ENSP00000390971.1:n.*589A>G
ENST00000533482.5:c.*2029A>G	ENSP00000431225.1:n.*2029A>G
NM_005732.3:c.2403A>G	NP_005723.2:p.Glu801=
NM_005732.4:c.2403A>G MANE Select	NP_005723.2:p.Glu801=