Canonical Allele Identifier: CA360934507

Gene: RAD50

Linked Data

• ClinVar Variation Id: 639921
• ClinVar RCV Id: RCV000792837
• dbSNP Id: rs1580987282
• MyVariant Identifiers: chr5:g.131915125A>T (hg19) ; chr5:g.132579433A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132579433A>T , CM000667.2:g.132579433A>T	GRCh38
NC_000005.9:g.131915125A>T , CM000667.1:g.131915125A>T	GRCh37
NC_000005.8:g.131943024A>T	NCBI36
NG_021151.1:g.27510A>T
NG_021151.2:g.27457A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.482A>T MANE Select	ENSP00000368100.4:p.Asp161Val
ENST00000638452.2:c.185A>T	ENSP00000492349.2:p.Asp62Val
ENST00000638504.1:n.442+3505A>T
ENST00000638568.2:c.185A>T	ENSP00000491158.2:p.Asp62Val
ENST00000639899.1:n.642A>T
ENST00000640655.2:c.185A>T	ENSP00000491596.2:p.Asp62Val
ENST00000651160.1:c.482A>T	ENSP00000498829.1:p.Asp161Val
ENST00000651541.1:c.185A>T	ENSP00000498795.1:p.Asp62Val
ENST00000651658.1:n.550A>T
ENST00000651723.1:c.*565A>T	ENSP00000498237.1:n.*565A>T
ENST00000652016.1:c.482A>T	ENSP00000498267.1:p.Asp161Val
ENST00000652485.1:c.482A>T	ENSP00000498973.1:p.Asp161Val
ENST00000378823.7:c.482A>T	ENSP00000368100.4:p.Asp161Val
ENST00000416135.5:c.185A>T	ENSP00000389515.1:p.Asp62Val
ENST00000423956.5:c.482A>T	ENSP00000390971.1:p.Asp161Val
ENST00000453394.5:c.482A>T	ENSP00000400049.1:p.Asp161Val
ENST00000533482.5:c.*108A>T	ENSP00000431225.1:n.*108A>T
NM_005732.3:c.482A>T	NP_005723.2:p.Asp161Val
NM_005732.4:c.482A>T MANE Select	NP_005723.2:p.Asp161Val