Canonical Allele Identifier: CA360946271

Gene: RAD50

Linked Data

• dbSNP Id: rs2149842613
• gnomAD v4: 5-132591878-C-A
• MyVariant Identifiers: chr5:g.131927570C>A (hg19) ; chr5:g.132591878C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132591878C>A , CM000667.2:g.132591878C>A	GRCh38
NC_000005.9:g.131927570C>A , CM000667.1:g.131927570C>A	GRCh37
NC_000005.8:g.131955469C>A	NCBI36
NG_021151.1:g.39955C>A
NG_021151.2:g.39902C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.1637C>A MANE Select	ENSP00000368100.4:p.Ala546Asp
ENST00000638452.2:c.1340C>A	ENSP00000492349.2:p.Ala447Asp
ENST00000638504.1:n.1323C>A
ENST00000638568.2:c.1340C>A	ENSP00000491158.2:p.Ala447Asp
ENST00000639899.1:n.2156C>A
ENST00000640655.2:c.1340C>A	ENSP00000491596.2:p.Ala447Asp
ENST00000651160.1:c.1637C>A	ENSP00000498829.1:p.Ala546Asp
ENST00000651541.1:c.1340C>A	ENSP00000498795.1:p.Ala447Asp
ENST00000651658.1:n.2064C>A
ENST00000651723.1:c.*1720C>A	ENSP00000498237.1:n.*1720C>A
ENST00000652016.1:c.1637C>A	ENSP00000498267.1:p.Ala546Asp
ENST00000652485.1:c.1670C>A	ENSP00000498973.1:p.Ala557Asp
ENST00000378823.7:c.1637C>A	ENSP00000368100.4:p.Ala546Asp
ENST00000423956.5:c.1635+472C>A	ENSP00000390971.1:n.1635+472C>A
ENST00000434288.1:c.132C>A
ENST00000453394.5:c.1454C>A	ENSP00000400049.1:p.Ala485Asp
ENST00000533482.5:c.*1263C>A	ENSP00000431225.1:n.*1263C>A
NM_005732.3:c.1637C>A	NP_005723.2:p.Ala546Asp
NM_005732.4:c.1637C>A MANE Select	NP_005723.2:p.Ala546Asp