Canonical Allele Identifier: CA360944648
Gene: RAD50 HGNC NCBI

Linked Data

ClinVar Variation Id: 819106
ClinVar RCV Id: RCV001011363
dbSNP Id: rs1554098329

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132589783G>T , CM000667.2:g.132589783G>T GRCh38
NC_000005.9:g.131925475G>T , CM000667.1:g.131925475G>T GRCh37
NC_000005.8:g.131953374G>T NCBI36
NG_021151.1:g.37860G>T
NG_021151.2:g.37807G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378823.8:c.1398G>T MANE Select ENSP00000368100.4:p.Gln466His
ENST00000638452.2:c.1101G>T ENSP00000492349.2:p.Gln367His
ENST00000638504.1:n.1084G>T
ENST00000638568.2:c.1101G>T ENSP00000491158.2:p.Gln367His
ENST00000639899.1:n.1917G>T
ENST00000640655.2:c.1101G>T ENSP00000491596.2:p.Gln367His
ENST00000651160.1:c.1398G>T ENSP00000498829.1:p.Gln466His
ENST00000651541.1:c.1101G>T ENSP00000498795.1:p.Gln367His
ENST00000651658.1:n.1825G>T
ENST00000651723.1:c.*1481G>T ENSP00000498237.1:n.*1481G>T
ENST00000652016.1:c.1398G>T ENSP00000498267.1:p.Gln466His
ENST00000652485.1:c.1398G>T ENSP00000498973.1:p.Gln466His
ENST00000378823.7:c.1398G>T ENSP00000368100.4:p.Gln466His
ENST00000423956.5:c.1398G>T ENSP00000390971.1:p.Gln466His
ENST00000453394.5:c.1398G>T ENSP00000400049.1:p.Gln466His
ENST00000533482.5:c.*1024G>T ENSP00000431225.1:n.*1024G>T
NM_005732.3:c.1398G>T NP_005723.2:p.Gln466His
NM_005732.4:c.1398G>T MANE Select NP_005723.2:p.Gln466His