Canonical Allele Identifier: CA2963251050
Gene: RAD51D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35101208dup , CM000679.2:g.35101208dup GRCh38
NC_000017.10:g.33428227dup , CM000679.1:g.33428227dup GRCh37
NC_000017.9:g.30452340dup NCBI36
NG_031858.1:g.23664dup , LRG_516:g.23664dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000586186.3:c.763dup ENSP00000468273.3:p.Arg255ProfsTer27
ENST00000587405.6:c.541dup ENSP00000466478.2:p.Arg181ProfsTer27
ENST00000590016.6:c.958dup ENSP00000466399.1:p.Arg320ProfsTer27
ENST00000592577.6:c.541dup ENSP00000466839.2:p.Arg181ProfsTer27
ENST00000345365.11:c.898dup MANE Select ENSP00000338790.6:p.Arg300ProfsTer27
ENST00000335858.11:c.562dup ENSP00000338408.6:p.Arg188ProfsTer27
ENST00000345365.10:c.898dup ENSP00000338790.6:p.Arg300ProfsTer27
ENST00000394589.8:c.898dup ENSP00000378090.4:p.Arg300ProfsTer27
ENST00000460118.6:c.367dup ENSP00000464356.2:p.Arg123ProfsTer27
ENST00000586044.5:c.*629dup ENSP00000465584.1:n.*629dup
ENST00000586210.5:c.*492dup ENSP00000465612.1:n.*492dup
ENST00000587977.5:c.*638dup ENSP00000466587.1:n.*638dup
ENST00000588372.5:c.*381dup ENSP00000468764.1:n.*381dup
ENST00000588594.5:c.*494dup ENSP00000465366.1:n.*494dup
ENST00000590016.5:c.958dup ENSP00000466399.1:p.Arg320ProfsTer27
ENST00000591723.5:c.367dup ENSP00000467986.1:p.Arg123ProfsTer5
ENST00000592181.1:c.541dup ENSP00000464799.1:p.Arg181ProfsTer?
ENST00000593039.5:c.421dup ENSP00000466834.1:p.Arg141ProfsTer5
NM_001142571.1:c.958dup NP_001136043.1:p.Arg320ProfsTer27
NM_002878.3:c.898dup , LRG_516t1:c.898dup NP_002869.3:p.Arg300ProfsTer27
NM_133629.2:c.562dup NP_598332.1:p.Arg188ProfsTer27
NR_037711.1:n.1035dup
NR_037712.1:n.900dup
NR_037714.1:n.650dup
NM_001142571.2:c.958dup NP_001136043.1:p.Arg320ProfsTer27
NM_133629.3:c.562dup NP_598332.1:p.Arg188ProfsTer27
NR_037711.2:n.924dup
NR_037712.2:n.789dup
NM_002878.4:c.898dup MANE Select NP_002869.3:p.Arg300ProfsTer27