Canonical Allele Identifier: CA2573054411

Gene: RAD51D

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35106395_35106398del , CM000679.2:g.35106395_35106398del	GRCh38
NC_000017.10:g.33433414_33433417del , CM000679.1:g.33433414_33433417del	GRCh37
NC_000017.9:g.30457527_30457530del	NCBI36
NG_031858.1:g.18472_18475del , LRG_516:g.18472_18475del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.429_432del	ENSP00000468273.3:p.Val144ProfsTer4
ENST00000587405.6:c.207_210del	ENSP00000466478.2:p.Val70ProfsTer4
ENST00000590016.6:c.624_627del	ENSP00000466399.1:p.Val209ProfsTer4
ENST00000590631.2:n.520_523del
ENST00000592577.6:c.207_210del	ENSP00000466839.2:p.Val70ProfsTer4
ENST00000345365.11:c.564_567del MANE Select	ENSP00000338790.6:p.Val189ProfsTer4
ENST00000335858.11:c.228_231del	ENSP00000338408.6:p.Val77ProfsTer4
ENST00000345365.10:c.564_567del	ENSP00000338790.6:p.Val189ProfsTer4
ENST00000394589.8:c.564_567del	ENSP00000378090.4:p.Val189ProfsTer4
ENST00000415064.6:n.714_717del
ENST00000460118.6:c.33_36del	ENSP00000464356.2:p.Val12ProfsTer4
ENST00000585947.5:n.460_463del
ENST00000585982.5:n.584_587del
ENST00000586044.5:c.*295_*298del	ENSP00000465584.1:n.*295_*298del
ENST00000586210.5:c.*158_*161del	ENSP00000465612.1:n.*158_*161del
ENST00000587405.5:c.207_210del	ENSP00000466478.1:p.Val70ProfsTer4
ENST00000587977.5:c.*304_*307del	ENSP00000466587.1:n.*304_*307del
ENST00000587982.5:n.357_360del
ENST00000588372.5:c.207_210del	ENSP00000468764.1:p.Val70ProfsTer10
ENST00000588594.5:c.*160_*163del	ENSP00000465366.1:n.*160_*163del
ENST00000590016.5:c.624_627del	ENSP00000466399.1:p.Val209ProfsTer4
ENST00000590631.1:c.33_36del	ENSP00000465033.1:p.Val12ProfsTer4
ENST00000591723.5:c.33_36del	ENSP00000467986.1:p.Val12ProfsTer4
ENST00000592181.1:c.207_210del	ENSP00000464799.1:p.Val70ProfsTer4
ENST00000592430.5:n.533_536del
ENST00000592577.5:c.570_573del	ENSP00000466839.1:p.Val191ProfsTer4
ENST00000593039.5:c.87_90del	ENSP00000466834.1:p.Val30ProfsTer4
NM_001142571.1:c.624_627del	NP_001136043.1:p.Val209ProfsTer4
NM_002878.3:c.564_567del , LRG_516t1:c.564_567del	NP_002869.3:p.Val189ProfsTer4
NM_133629.2:c.228_231del	NP_598332.1:p.Val77ProfsTer4
NR_037711.1:n.701_704del
NR_037712.1:n.566_569del
NR_037714.1:n.316_319del
NM_001142571.2:c.624_627del	NP_001136043.1:p.Val209ProfsTer4
NM_133629.3:c.228_231del	NP_598332.1:p.Val77ProfsTer4
NR_037711.2:n.590_593del
NR_037712.2:n.455_458del
NM_002878.4:c.564_567del MANE Select	NP_002869.3:p.Val189ProfsTer4