Canonical Allele Identifier: CA16622123
Gene: RAD51D HGNC NCBI

Linked Data

ClinVar Variation Id: 480540
dbSNP Id: rs1555567610

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35103498dup , CM000679.2:g.35103498dup GRCh38
NC_000017.10:g.33430517dup , CM000679.1:g.33430517dup GRCh37
NC_000017.9:g.30454630dup NCBI36
NG_031858.1:g.21372dup , LRG_516:g.21372dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000586186.3:c.488dup ENSP00000468273.3:p.Thr164HisfsTer?
ENST00000587405.6:c.266dup ENSP00000466478.2:p.Thr90HisfsTer?
ENST00000590016.6:c.683dup ENSP00000466399.1:p.Thr229HisfsTer?
ENST00000592577.6:c.266dup ENSP00000466839.2:p.Thr90HisfsTer?
ENST00000345365.11:c.623dup MANE Select ENSP00000338790.6:p.Thr209HisfsTer?
ENST00000335858.11:c.287dup ENSP00000338408.6:p.Thr97HisfsTer?
ENST00000345365.10:c.623dup ENSP00000338790.6:p.Thr209HisfsTer?
ENST00000394589.8:c.623dup ENSP00000378090.4:p.Thr209HisfsTer?
ENST00000460118.6:c.92dup ENSP00000464356.2:p.Thr32HisfsTer?
ENST00000586044.5:c.*354dup ENSP00000465584.1:n.*354dup
ENST00000586210.5:c.*217dup ENSP00000465612.1:n.*217dup
ENST00000587405.5:c.266dup ENSP00000466478.1:p.Thr90HisfsTer?
ENST00000587977.5:c.*363dup ENSP00000466587.1:n.*363dup
ENST00000588372.5:c.*106dup ENSP00000468764.1:n.*106dup
ENST00000588594.5:c.*219dup ENSP00000465366.1:n.*219dup
ENST00000590016.5:c.683dup ENSP00000466399.1:p.Thr229HisfsTer?
ENST00000591723.5:c.92dup ENSP00000467986.1:p.Thr32HisfsTer?
ENST00000592181.1:c.266dup ENSP00000464799.1:p.Thr90HisfsTer?
ENST00000592577.5:c.629dup ENSP00000466839.1:p.Thr211HisfsTer?
ENST00000593039.5:c.146dup ENSP00000466834.1:p.Thr50HisfsTer?
NM_001142571.1:c.683dup NP_001136043.1:p.Thr229HisfsTer?
NM_002878.3:c.623dup , LRG_516t1:c.623dup NP_002869.3:p.Thr209HisfsTer?
NM_133629.2:c.287dup NP_598332.1:p.Thr97HisfsTer?
NR_037711.1:n.760dup
NR_037712.1:n.625dup
NR_037714.1:n.375dup
NM_001142571.2:c.683dup NP_001136043.1:p.Thr229HisfsTer?
NM_133629.3:c.287dup NP_598332.1:p.Thr97HisfsTer?
NR_037711.2:n.649dup
NR_037712.2:n.514dup
NM_002878.4:c.623dup MANE Select NP_002869.3:p.Thr209HisfsTer?