Canonical Allele Identifier: CA2580093465

Gene: RAD51D

Linked Data

• ClinVar Variation Id: 1756210
• ClinVar RCV Id: RCV002362393

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35103298_35103299delinsAA , CM000679.2:g.35103298_35103299delinsAA	GRCh38
NC_000017.10:g.33430317_33430318delinsAA , CM000679.1:g.33430317_33430318delinsAA	GRCh37
NC_000017.9:g.30454430_30454431delinsAA	NCBI36
NG_031858.1:g.21571_21572delinsTT , LRG_516:g.21571_21572delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.558_559delinsTT	ENSP00000468273.3:p.Ala187Ter
ENST00000587405.6:c.336_337delinsTT	ENSP00000466478.2:p.Ala113Ter
ENST00000590016.6:c.753_754delinsTT	ENSP00000466399.1:p.Ala252Ter
ENST00000592577.6:c.336_337delinsTT	ENSP00000466839.2:p.Ala113Ter
ENST00000345365.11:c.693_694delinsTT MANE Select	ENSP00000338790.6:p.Ala232Ter
ENST00000335858.11:c.357_358delinsTT	ENSP00000338408.6:p.Ala120Ter
ENST00000345365.10:c.693_694delinsTT	ENSP00000338790.6:p.Ala232Ter
ENST00000394589.8:c.693_694delinsTT	ENSP00000378090.4:p.Ala232Ter
ENST00000460118.6:c.162_163delinsTT	ENSP00000464356.2:p.Ala55Ter
ENST00000586044.5:c.*424_*425delinsTT	ENSP00000465584.1:n.*424_*425delinsTT
ENST00000586210.5:c.*287_*288delinsTT	ENSP00000465612.1:n.*287_*288delinsTT
ENST00000587405.5:c.336_337delinsTT	ENSP00000466478.1:p.Ala113Ter
ENST00000587977.5:c.*433_*434delinsTT	ENSP00000466587.1:n.*433_*434delinsTT
ENST00000588372.5:c.*176_*177delinsTT	ENSP00000468764.1:n.*176_*177delinsTT
ENST00000588594.5:c.*289_*290delinsTT	ENSP00000465366.1:n.*289_*290delinsTT
ENST00000590016.5:c.753_754delinsTT	ENSP00000466399.1:p.Ala252Ter
ENST00000591723.5:c.162_163delinsTT	ENSP00000467986.1:p.Ala55Ter
ENST00000592181.1:c.336_337delinsTT	ENSP00000464799.1:p.Ala113Ter
ENST00000592577.5:c.699_700delinsTT	ENSP00000466839.1:p.Ala234Ter
ENST00000593039.5:c.216_217delinsTT	ENSP00000466834.1:p.Ala73Ter
NM_001142571.1:c.753_754delinsTT	NP_001136043.1:p.Ala252Ter
NM_002878.3:c.693_694delinsTT , LRG_516t1:c.693_694delinsTT	NP_002869.3:p.Ala232Ter
NM_133629.2:c.357_358delinsTT	NP_598332.1:p.Ala120Ter
NR_037711.1:n.830_831delinsTT
NR_037712.1:n.695_696delinsTT
NR_037714.1:n.445_446delinsTT
NM_001142571.2:c.753_754delinsTT	NP_001136043.1:p.Ala252Ter
NM_133629.3:c.357_358delinsTT	NP_598332.1:p.Ala120Ter
NR_037711.2:n.719_720delinsTT
NR_037712.2:n.584_585delinsTT
NM_002878.4:c.693_694delinsTT MANE Select	NP_002869.3:p.Ala232Ter