Canonical Allele Identifier: CA16620380
Gene: RAD51D HGNC NCBI

Linked Data

ClinVar Variation Id: 421303
dbSNP Id: rs1064795045

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35101328_35101334del , CM000679.2:g.35101328_35101334del GRCh38
NC_000017.10:g.33428347_33428353del , CM000679.1:g.33428347_33428353del GRCh37
NC_000017.9:g.30452460_30452466del NCBI36
NG_031858.1:g.23538_23544del , LRG_516:g.23538_23544del

Transcript Alleles

HGVS Amino-acid change
ENST00000586186.3:c.637_643del ENSP00000468273.3:p.Gly213SerfsTer?
ENST00000587405.6:c.415_421del ENSP00000466478.2:p.Gly139SerfsTer?
ENST00000590016.6:c.832_838del ENSP00000466399.1:p.Gly278SerfsTer?
ENST00000592577.6:c.415_421del ENSP00000466839.2:p.Gly139SerfsTer?
ENST00000345365.11:c.772_778del MANE Select ENSP00000338790.6:p.Gly258SerfsTer?
ENST00000335858.11:c.436_442del ENSP00000338408.6:p.Gly146SerfsTer?
ENST00000345365.10:c.772_778del ENSP00000338790.6:p.Gly258SerfsTer?
ENST00000394589.8:c.772_778del ENSP00000378090.4:p.Gly258SerfsTer?
ENST00000460118.6:c.241_247del ENSP00000464356.2:p.Gly81SerfsTer?
ENST00000586044.5:c.*503_*509del ENSP00000465584.1:n.*503_*509del
ENST00000586210.5:c.*366_*372del ENSP00000465612.1:n.*366_*372del
ENST00000587405.5:c.415_421del ENSP00000466478.1:p.Gly139=
ENST00000587977.5:c.*512_*518del ENSP00000466587.1:n.*512_*518del
ENST00000588372.5:c.*255_*261del ENSP00000468764.1:n.*255_*261del
ENST00000588594.5:c.*368_*374del ENSP00000465366.1:n.*368_*374del
ENST00000590016.5:c.832_838del ENSP00000466399.1:p.Gly278SerfsTer?
ENST00000591723.5:c.241_247del ENSP00000467986.1:p.Gly81SerfsTer?
ENST00000592181.1:c.415_421del ENSP00000464799.1:p.Gly139SerfsTer?
ENST00000593039.5:c.295_301del ENSP00000466834.1:p.Gly99SerfsTer?
NM_001142571.1:c.832_838del NP_001136043.1:p.Gly278SerfsTer?
NM_002878.3:c.772_778del , LRG_516t1:c.772_778del NP_002869.3:p.Gly258SerfsTer?
NM_133629.2:c.436_442del NP_598332.1:p.Gly146SerfsTer?
NR_037711.1:n.909_915del
NR_037712.1:n.774_780del
NR_037714.1:n.524_530del
NM_001142571.2:c.832_838del NP_001136043.1:p.Gly278SerfsTer?
NM_133629.3:c.436_442del NP_598332.1:p.Gly146SerfsTer?
NR_037711.2:n.798_804del
NR_037712.2:n.663_669del
NM_002878.4:c.772_778del MANE Select NP_002869.3:p.Gly258SerfsTer?