Canonical Allele Identifier: CA360956556

Gene: RAD50

Linked Data

• MyVariant Identifiers: chr5:g.131940584A>G (hg19) ; chr5:g.132604892A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132604892A>G , CM000667.2:g.132604892A>G	GRCh38
NC_000005.9:g.131940584A>G , CM000667.1:g.131940584A>G	GRCh37
NC_000005.8:g.131968483A>G	NCBI36
NG_021151.1:g.52969A>G
NG_021151.2:g.52916A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.2611A>G MANE Select	ENSP00000368100.4:p.Lys871Glu
ENST00000638452.2:c.2314A>G	ENSP00000492349.2:p.Lys772Glu
ENST00000638504.1:n.2219A>G
ENST00000638568.2:c.2314A>G	ENSP00000491158.2:p.Lys772Glu
ENST00000639899.1:n.3130A>G
ENST00000640655.2:c.2314A>G	ENSP00000491596.2:p.Lys772Glu
ENST00000651160.1:c.*755A>G	ENSP00000498829.1:n.*755A>G
ENST00000651723.1:c.*2694A>G	ENSP00000498237.1:n.*2694A>G
ENST00000652016.1:c.*828A>G	ENSP00000498267.1:n.*828A>G
ENST00000652485.1:c.2644A>G	ENSP00000498973.1:p.Lys882Glu
ENST00000378823.7:c.2611A>G	ENSP00000368100.4:p.Lys871Glu
ENST00000423956.5:c.*797A>G	ENSP00000390971.1:n.*797A>G
ENST00000533482.5:c.*2237A>G	ENSP00000431225.1:n.*2237A>G
NM_005732.3:c.2611A>G	NP_005723.2:p.Lys871Glu
NM_005732.4:c.2611A>G MANE Select	NP_005723.2:p.Lys871Glu