Canonical Allele Identifier: CA360955894

Gene: RAD50

Linked Data

• MyVariant Identifiers: chr5:g.131939724A>G (hg19) ; chr5:g.132604032A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132604032A>G , CM000667.2:g.132604032A>G	GRCh38
NC_000005.9:g.131939724A>G , CM000667.1:g.131939724A>G	GRCh37
NC_000005.8:g.131967623A>G	NCBI36
NG_021151.1:g.52109A>G
NG_021151.2:g.52056A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.2510A>G MANE Select	ENSP00000368100.4:p.His837Arg
ENST00000638452.2:c.2213A>G	ENSP00000492349.2:p.His738Arg
ENST00000638504.1:n.2118A>G
ENST00000638568.2:c.2213A>G	ENSP00000491158.2:p.His738Arg
ENST00000639899.1:n.3029A>G
ENST00000640655.2:c.2213A>G	ENSP00000491596.2:p.His738Arg
ENST00000651160.1:c.*654A>G	ENSP00000498829.1:n.*654A>G
ENST00000651658.1:n.3053A>G
ENST00000651723.1:c.*2593A>G	ENSP00000498237.1:n.*2593A>G
ENST00000652016.1:c.*727A>G	ENSP00000498267.1:n.*727A>G
ENST00000652485.1:c.2543A>G	ENSP00000498973.1:p.His848Arg
ENST00000378823.7:c.2510A>G	ENSP00000368100.4:p.His837Arg
ENST00000423956.5:c.*696A>G	ENSP00000390971.1:n.*696A>G
ENST00000533482.5:c.*2136A>G	ENSP00000431225.1:n.*2136A>G
NM_005732.3:c.2510A>G	NP_005723.2:p.His837Arg
NM_005732.4:c.2510A>G MANE Select	NP_005723.2:p.His837Arg