Canonical Allele Identifier: CA915949977

Gene: RAD51D

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35103270_35103303del , CM000679.2:g.35103270_35103303del	GRCh38
NC_000017.10:g.33430289_33430322del , CM000679.1:g.33430289_33430322del	GRCh37
NC_000017.9:g.30454402_30454435del	NCBI36
NG_031858.1:g.21571_21604del , LRG_516:g.21571_21604del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.558_591del	ENSP00000468273.3:p.Arg187TrpfsTer5
ENST00000587405.6:c.336_369del	ENSP00000466478.2:p.Arg113TrpfsTer5
ENST00000590016.6:c.753_786del	ENSP00000466399.1:p.Arg252TrpfsTer5
ENST00000592577.6:c.336_369del	ENSP00000466839.2:p.Arg113TrpfsTer5
ENST00000345365.11:c.693_726del MANE Select	ENSP00000338790.6:p.Arg232TrpfsTer5
ENST00000335858.11:c.357_390del	ENSP00000338408.6:p.Arg120TrpfsTer5
ENST00000345365.10:c.693_726del	ENSP00000338790.6:p.Arg232TrpfsTer5
ENST00000394589.8:c.693_726del	ENSP00000378090.4:p.Arg232TrpfsTer5
ENST00000460118.6:c.162_195del	ENSP00000464356.2:p.Arg55TrpfsTer5
ENST00000586044.5:c.*424_*457del	ENSP00000465584.1:n.*424_*457del
ENST00000586210.5:c.*287_*320del	ENSP00000465612.1:n.*287_*320del
ENST00000587405.5:c.336_369del	ENSP00000466478.1:p.Arg113TrpfsTer5
ENST00000587977.5:c.*433_*466del	ENSP00000466587.1:n.*433_*466del
ENST00000588372.5:c.*176_*209del	ENSP00000468764.1:n.*176_*209del
ENST00000588594.5:c.*289_*322del	ENSP00000465366.1:n.*289_*322del
ENST00000590016.5:c.753_786del	ENSP00000466399.1:p.Arg252TrpfsTer5
ENST00000591723.5:c.162_195del	ENSP00000467986.1:p.Arg55TrpfsTer5
ENST00000592181.1:c.336_369del	ENSP00000464799.1:p.Arg113TrpfsTer5
ENST00000592577.5:c.699_732del	ENSP00000466839.1:p.Arg234TrpfsTer5
ENST00000593039.5:c.216_249del	ENSP00000466834.1:p.Arg73TrpfsTer5
NM_001142571.1:c.753_786del	NP_001136043.1:p.Arg252TrpfsTer5
NM_002878.3:c.693_726del , LRG_516t1:c.693_726del	NP_002869.3:p.Arg232TrpfsTer5
NM_133629.2:c.357_390del	NP_598332.1:p.Arg120TrpfsTer5
NR_037711.1:n.830_863del
NR_037712.1:n.695_728del
NR_037714.1:n.445_478del
NM_001142571.2:c.753_786del	NP_001136043.1:p.Arg252TrpfsTer5
NM_133629.3:c.357_390del	NP_598332.1:p.Arg120TrpfsTer5
NR_037711.2:n.719_752del
NR_037712.2:n.584_617del
NM_002878.4:c.693_726del MANE Select	NP_002869.3:p.Arg232TrpfsTer5