Canonical Allele Identifier: CA127258056

Gene: RAD50

Linked Data

• ClinVar Variation Id: 457408
• ClinVar RCV Id: RCV000552241
• dbSNP Id: rs1040611482
• gnomAD v2: 5-131939713-A-G
• gnomAD v3: 5-132604021-A-G
• gnomAD v4: 5-132604021-A-G
• MyVariant Identifiers: chr5:g.131939713A>G (hg19) ; chr5:g.132604021A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132604021A>G , CM000667.2:g.132604021A>G	GRCh38
NC_000005.9:g.131939713A>G , CM000667.1:g.131939713A>G	GRCh37
NC_000005.8:g.131967612A>G	NCBI36
NG_021151.1:g.52098A>G
NG_021151.2:g.52045A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.2499A>G MANE Select	ENSP00000368100.4:p.Gln833=
ENST00000638452.2:c.2202A>G	ENSP00000492349.2:p.Gln734=
ENST00000638504.1:n.2107A>G
ENST00000638568.2:c.2202A>G	ENSP00000491158.2:p.Gln734=
ENST00000639899.1:n.3018A>G
ENST00000640655.2:c.2202A>G	ENSP00000491596.2:p.Gln734=
ENST00000651160.1:c.*643A>G	ENSP00000498829.1:n.*643A>G
ENST00000651658.1:n.3042A>G
ENST00000651723.1:c.*2582A>G	ENSP00000498237.1:n.*2582A>G
ENST00000652016.1:c.*716A>G	ENSP00000498267.1:n.*716A>G
ENST00000652485.1:c.2532A>G	ENSP00000498973.1:p.Gln844=
ENST00000378823.7:c.2499A>G	ENSP00000368100.4:p.Gln833=
ENST00000423956.5:c.*685A>G	ENSP00000390971.1:n.*685A>G
ENST00000533482.5:c.*2125A>G	ENSP00000431225.1:n.*2125A>G
NM_005732.3:c.2499A>G	NP_005723.2:p.Gln833=
NM_005732.4:c.2499A>G MANE Select	NP_005723.2:p.Gln833=