Canonical Allele Identifier: CA360956849

Gene: RAD50

Linked Data

• MyVariant Identifiers: chr5:g.131940651A>G (hg19) ; chr5:g.132604959A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132604959A>G , CM000667.2:g.132604959A>G	GRCh38
NC_000005.9:g.131940651A>G , CM000667.1:g.131940651A>G	GRCh37
NC_000005.8:g.131968550A>G	NCBI36
NG_021151.1:g.53036A>G
NG_021151.2:g.52983A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.2678A>G MANE Select	ENSP00000368100.4:p.Glu893Gly
ENST00000638452.2:c.2381A>G	ENSP00000492349.2:p.Glu794Gly
ENST00000638504.1:n.2286A>G
ENST00000638568.2:c.2381A>G	ENSP00000491158.2:p.Glu794Gly
ENST00000639899.1:n.3197A>G
ENST00000640655.2:c.2381A>G	ENSP00000491596.2:p.Glu794Gly
ENST00000651160.1:c.*822A>G	ENSP00000498829.1:n.*822A>G
ENST00000651723.1:c.*2761A>G	ENSP00000498237.1:n.*2761A>G
ENST00000652016.1:c.*895A>G	ENSP00000498267.1:n.*895A>G
ENST00000378823.7:c.2678A>G	ENSP00000368100.4:p.Glu893Gly
ENST00000423956.5:c.*864A>G	ENSP00000390971.1:n.*864A>G
ENST00000533482.5:c.*2304A>G	ENSP00000431225.1:n.*2304A>G
NM_005732.3:c.2678A>G	NP_005723.2:p.Glu893Gly
NM_005732.4:c.2678A>G MANE Select	NP_005723.2:p.Glu893Gly