Canonical Allele Identifier: CA2573054405

Gene: RAD51D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35100953_35101035del , CM000679.2:g.35100953_35101035del	GRCh38
NC_000017.10:g.33427972_33428054del , CM000679.1:g.33427972_33428054del	GRCh37
NC_000017.9:g.30452085_30452167del	NCBI36
NG_031858.1:g.23836_23918del , LRG_516:g.23836_23918del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.771_*1del	ENSP00000468273.3:n.[c.771_*1del;Thr258CysfsTer?]
ENST00000587405.6:c.549_*1del	ENSP00000466478.2:n.[c.549_*1del;Thr184CysfsTer?]
ENST00000590016.6:c.966_*1del	ENSP00000466399.1:n.[c.966_*1del;Thr323CysfsTer?]
ENST00000592577.6:c.549_*1del	ENSP00000466839.2:n.[c.549_*1del;Thr184CysfsTer?]
ENST00000345365.11:c.906_*1del MANE Select	ENSP00000338790.6:n.[c.906_*1del;Thr303CysfsTer?]
ENST00000335858.11:c.570_*1del	ENSP00000338408.6:n.[c.570_*1del;Thr191CysfsTer?]
ENST00000345365.10:c.906_*1del	ENSP00000338790.6:n.[c.906_*1del;Thr303CysfsTer?]
ENST00000394589.8:c.906_*1del	ENSP00000378090.4:n.[c.906_*1del;Thr303CysfsTer?]
ENST00000460118.6:c.375_*1del	ENSP00000464356.2:n.[c.375_*1del;Thr126CysfsTer?]
ENST00000586044.5:c.*637_*719del	ENSP00000465584.1:n.*637_*719del
ENST00000586210.5:c.*500_*582del	ENSP00000465612.1:n.*500_*582del
ENST00000587977.5:c.*646_*728del	ENSP00000466587.1:n.*646_*728del
ENST00000588372.5:c.*389_*471del	ENSP00000468764.1:n.*389_*471del
ENST00000588594.5:c.*502_*584del	ENSP00000465366.1:n.*502_*584del
ENST00000590016.5:c.966_*1del	ENSP00000466399.1:n.[c.966_*1del;Thr323CysfsTer?]
ENST00000591723.5:c.372+167_372+249del	ENSP00000467986.1:n.372+167_372+249del
ENST00000592181.1:c.546+167_546+249del	ENSP00000464799.1:n.546+167_546+249del
ENST00000593039.5:c.426+167_426+249del	ENSP00000466834.1:n.426+167_426+249del
NM_001142571.1:c.966_*1del	NP_001136043.1:n.[c.966_*1del;Thr323CysfsTer?]
NM_002878.3:c.906_*1del , LRG_516t1:c.906_*1del	NP_002869.3:n.[c.906_*1del;Thr303CysfsTer?]
NM_133629.2:c.570_*1del	NP_598332.1:n.[c.570_*1del;Thr191CysfsTer?]
NR_037711.1:n.1043_1125del
NR_037712.1:n.908_990del
NR_037714.1:n.655+167_655+249del
NM_001142571.2:c.966_*1del	NP_001136043.1:n.[c.966_*1del;Thr323CysfsTer?]
NM_133629.3:c.570_*1del	NP_598332.1:n.[c.570_*1del;Thr191CysfsTer?]
NR_037711.2:n.932_1014del
NR_037712.2:n.797_879del
NM_002878.4:c.906_*1del MANE Select	NP_002869.3:n.[c.906_*1del;Thr303CysfsTer?]