Canonical Allele Identifier: CA2580093459

Gene: RAD51D

Linked Data

• ClinVar Variation Id: 1756261
• ClinVar RCV Id: RCV002362433

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35103277_35103298delinsAGGCCAGGGTCTTCAGCTCTCA , CM000679.2:g.35103277_35103298delinsAGGCCAGGGTCTTCAGCTCTCA	GRCh38
NC_000017.10:g.33430296_33430317delinsAGGCCAGGGTCTTCAGCTCTCA , CM000679.1:g.33430296_33430317delinsAGGCCAGGGTCTTCAGCTCTCA	GRCh37
NC_000017.9:g.30454409_30454430delinsAGGCCAGGGTCTTCAGCTCTCA	NCBI36
NG_031858.1:g.21572_21593delinsTGAGAGCTGAAGACCCTGGCCT , LRG_516:g.21572_21593delinsTGAGAGCTGAAGACCCTGGCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.559_580delinsTGAGAGCTGAAGACCCTGGCCT	ENSP00000468273.3:p.Arg187Ter
ENST00000587405.6:c.337_358delinsTGAGAGCTGAAGACCCTGGCCT	ENSP00000466478.2:p.Arg113Ter
ENST00000590016.6:c.754_775delinsTGAGAGCTGAAGACCCTGGCCT	ENSP00000466399.1:p.Arg252Ter
ENST00000592577.6:c.337_358delinsTGAGAGCTGAAGACCCTGGCCT	ENSP00000466839.2:p.Arg113Ter
ENST00000345365.11:c.694_715delinsTGAGAGCTGAAGACCCTGGCCT MANE Select	ENSP00000338790.6:p.Arg232Ter
ENST00000335858.11:c.358_379delinsTGAGAGCTGAAGACCCTGGCCT	ENSP00000338408.6:p.Arg120Ter
ENST00000345365.10:c.694_715delinsTGAGAGCTGAAGACCCTGGCCT	ENSP00000338790.6:p.Arg232Ter
ENST00000394589.8:c.694_715delinsTGAGAGCTGAAGACCCTGGCCT	ENSP00000378090.4:p.Arg232Ter
ENST00000460118.6:c.163_184delinsTGAGAGCTGAAGACCCTGGCCT	ENSP00000464356.2:p.Arg55Ter
ENST00000586044.5:c.*425_*446delinsTGAGAGCTGAAGACCCTGGCCT	ENSP00000465584.1:n.*425_*446delinsTGAGAGCTGAAGACCCTGGCCT
ENST00000586210.5:c.*288_*309delinsTGAGAGCTGAAGACCCTGGCCT	ENSP00000465612.1:n.*288_*309delinsTGAGAGCTGAAGACCCTGGCCT
ENST00000587405.5:c.337_358delinsTGAGAGCTGAAGACCCTGGCCT	ENSP00000466478.1:p.Arg113Ter
ENST00000587977.5:c.*434_*455delinsTGAGAGCTGAAGACCCTGGCCT	ENSP00000466587.1:n.*434_*455delinsTGAGAGCTGAAGACCCTGGCCT
ENST00000588372.5:c.*177_*198delinsTGAGAGCTGAAGACCCTGGCCT	ENSP00000468764.1:n.*177_*198delinsTGAGAGCTGAAGACCCTGGCCT
ENST00000588594.5:c.*290_*311delinsTGAGAGCTGAAGACCCTGGCCT	ENSP00000465366.1:n.*290_*311delinsTGAGAGCTGAAGACCCTGGCCT
ENST00000590016.5:c.754_775delinsTGAGAGCTGAAGACCCTGGCCT	ENSP00000466399.1:p.Arg252Ter
ENST00000591723.5:c.163_184delinsTGAGAGCTGAAGACCCTGGCCT	ENSP00000467986.1:p.Arg55Ter
ENST00000592181.1:c.337_358delinsTGAGAGCTGAAGACCCTGGCCT	ENSP00000464799.1:p.Arg113Ter
ENST00000592577.5:c.700_721delinsTGAGAGCTGAAGACCCTGGCCT	ENSP00000466839.1:p.Arg234Ter
ENST00000593039.5:c.217_238delinsTGAGAGCTGAAGACCCTGGCCT	ENSP00000466834.1:p.Arg73Ter
NM_001142571.1:c.754_775delinsTGAGAGCTGAAGACCCTGGCCT	NP_001136043.1:p.Arg252Ter
NM_002878.3:c.694_715delinsTGAGAGCTGAAGACCCTGGCCT , LRG_516t1:c.694_715delinsTGAGAGCTGAAGACCCTGGCCT	NP_002869.3:p.Arg232Ter
NM_133629.2:c.358_379delinsTGAGAGCTGAAGACCCTGGCCT	NP_598332.1:p.Arg120Ter
NR_037711.1:n.831_852delinsTGAGAGCTGAAGACCCTGGCCT
NR_037712.1:n.696_717delinsTGAGAGCTGAAGACCCTGGCCT
NR_037714.1:n.446_467delinsTGAGAGCTGAAGACCCTGGCCT
NM_001142571.2:c.754_775delinsTGAGAGCTGAAGACCCTGGCCT	NP_001136043.1:p.Arg252Ter
NM_133629.3:c.358_379delinsTGAGAGCTGAAGACCCTGGCCT	NP_598332.1:p.Arg120Ter
NR_037711.2:n.720_741delinsTGAGAGCTGAAGACCCTGGCCT
NR_037712.2:n.585_606delinsTGAGAGCTGAAGACCCTGGCCT
NM_002878.4:c.694_715delinsTGAGAGCTGAAGACCCTGGCCT MANE Select	NP_002869.3:p.Arg232Ter