Canonical Allele Identifier: CA192195
Gene: RAD51D HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000586186.3:c.763del ENSP00000468273.3:p.Arg255AspfsTer10
ENST00000587405.6:c.541del ENSP00000466478.2:p.Arg181AspfsTer10
ENST00000590016.6:c.958del ENSP00000466399.1:p.Arg320AspfsTer10
ENST00000592577.6:c.541del ENSP00000466839.2:p.Arg181AspfsTer10
ENST00000345365.11:c.898del MANE Select ENSP00000338790.6:p.Arg300AspfsTer10
ENST00000335858.11:c.562del ENSP00000338408.6:p.Arg188AspfsTer10
ENST00000345365.10:c.898del ENSP00000338790.6:p.Arg300AspfsTer10
ENST00000394589.8:c.898del ENSP00000378090.4:p.Arg300AspfsTer10
ENST00000460118.6:c.367del ENSP00000464356.2:p.Arg123AspfsTer10
ENST00000586044.5:c.*629del ENSP00000465584.1:n.*629del
ENST00000586210.5:c.*492del ENSP00000465612.1:n.*492del
ENST00000587977.5:c.*638del ENSP00000466587.1:n.*638del
ENST00000588372.5:c.*381del ENSP00000468764.1:n.*381del
ENST00000588594.5:c.*494del ENSP00000465366.1:n.*494del
ENST00000590016.5:c.958del ENSP00000466399.1:p.Arg320AspfsTer10
ENST00000591723.5:c.367del ENSP00000467986.1:p.Arg123AspfsTer?
ENST00000592181.1:c.541del ENSP00000464799.1:p.Arg181AspfsTer20
ENST00000593039.5:c.421del ENSP00000466834.1:p.Arg141AspfsTer21
NM_001142571.1:c.958del NP_001136043.1:p.Arg320AspfsTer10
NM_002878.3:c.898del , LRG_516t1:c.898del NP_002869.3:p.Arg300AspfsTer10
NM_133629.2:c.562del NP_598332.1:p.Arg188AspfsTer10
NR_037711.1:n.1035del
NR_037712.1:n.900del
NR_037714.1:n.650del
NM_001142571.2:c.958del NP_001136043.1:p.Arg320AspfsTer10
NM_133629.3:c.562del NP_598332.1:p.Arg188AspfsTer10
NR_037711.2:n.924del
NR_037712.2:n.789del
NM_002878.4:c.898del MANE Select NP_002869.3:p.Arg300AspfsTer10