Canonical Allele Identifier: CA360955865

Gene: RAD50

Linked Data

• MyVariant Identifiers: chr5:g.131939720C>A (hg19) ; chr5:g.132604028C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132604028C>A , CM000667.2:g.132604028C>A	GRCh38
NC_000005.9:g.131939720C>A , CM000667.1:g.131939720C>A	GRCh37
NC_000005.8:g.131967619C>A	NCBI36
NG_021151.1:g.52105C>A
NG_021151.2:g.52052C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.2506C>A MANE Select	ENSP00000368100.4:p.Gln836Lys
ENST00000638452.2:c.2209C>A	ENSP00000492349.2:p.Gln737Lys
ENST00000638504.1:n.2114C>A
ENST00000638568.2:c.2209C>A	ENSP00000491158.2:p.Gln737Lys
ENST00000639899.1:n.3025C>A
ENST00000640655.2:c.2209C>A	ENSP00000491596.2:p.Gln737Lys
ENST00000651160.1:c.*650C>A	ENSP00000498829.1:n.*650C>A
ENST00000651658.1:n.3049C>A
ENST00000651723.1:c.*2589C>A	ENSP00000498237.1:n.*2589C>A
ENST00000652016.1:c.*723C>A	ENSP00000498267.1:n.*723C>A
ENST00000652485.1:c.2539C>A	ENSP00000498973.1:p.Gln847Lys
ENST00000378823.7:c.2506C>A	ENSP00000368100.4:p.Gln836Lys
ENST00000423956.5:c.*692C>A	ENSP00000390971.1:n.*692C>A
ENST00000533482.5:c.*2132C>A	ENSP00000431225.1:n.*2132C>A
NM_005732.3:c.2506C>A	NP_005723.2:p.Gln836Lys
NM_005732.4:c.2506C>A MANE Select	NP_005723.2:p.Gln836Lys