Canonical Allele Identifier: CA2499224763

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 1073709
• ClinVar RCV Id: RCV001386782 ; RCV002420863 ; RCV004037683
• dbSNP Id: rs2143853617

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58709948del , CM000679.2:g.58709948del	GRCh38
NC_000017.10:g.56787309del , CM000679.1:g.56787309del	GRCh37
NC_000017.9:g.54142308del	NCBI36
NG_023199.1:g.22347del , LRG_314:g.22347del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.444del	ENSP00000464056.2:p.Ala149ProfsTer4
ENST00000697678.1:n.697del
ENST00000697679.1:n.1869del
ENST00000697680.1:c.*1659del	ENSP00000513392.1:n.*1659del
ENST00000697681.1:c.*1956del	ENSP00000513393.1:n.*1956del
ENST00000697683.1:c.*1659del	ENSP00000513395.1:n.*1659del
ENST00000697684.1:n.855del
ENST00000697685.1:c.*1492del	ENSP00000513396.1:n.*1492del
ENST00000697686.1:c.444del	ENSP00000513397.1:p.Ala149ProfsTer4
ENST00000697687.1:n.674del
ENST00000697688.1:n.841del
ENST00000697689.1:c.*1331del	ENSP00000513398.1:n.*1331del
ENST00000697690.1:c.795del	ENSP00000513399.1:p.Ala266ProfsTer4
ENST00000697691.1:c.*767del	ENSP00000513400.1:n.*767del
ENST00000697692.1:c.*807del	ENSP00000513401.1:n.*807del
ENST00000697694.1:c.444del	ENSP00000513402.1:p.Ala149ProfsTer4
ENST00000697695.1:n.1402del
ENST00000337432.9:c.795del MANE Select	ENSP00000336701.4:p.Ala266ProfsTer4
ENST00000337432.8:c.795del	ENSP00000336701.4:p.Ala266ProfsTer4
ENST00000413590.5:c.433del
ENST00000475762.5:c.*1498del	ENSP00000432421.1:n.*1498del
ENST00000482007.5:c.*223del	ENSP00000433332.1:n.*223del
ENST00000487525.5:c.*368del	ENSP00000431637.1:n.*368del
ENST00000578151.1:n.130del
ENST00000581221.5:n.310del
ENST00000583539.5:c.795del	ENSP00000463121.1:p.Ala266ProfsTer4
ENST00000584617.5:c.517del
ENST00000584804.1:c.90del	ENSP00000463658.1:p.Ala31ProfsTer4
NM_058216.2:c.795del	NP_478123.1:p.Ala266ProfsTer4
NR_103872.1:n.699del
XM_006722001.2:c.795del	XP_006722064.1:p.Ala266ProfsTer4
XM_006722002.2:c.795del	XP_006722065.1:p.Ala266ProfsTer4
XM_006722004.2:c.444del	XP_006722067.1:p.Ala149ProfsTer4
XM_006722005.2:c.444del	XP_006722068.1:p.Ala149ProfsTer4
XM_011525092.1:c.444del	XP_011523394.1:p.Ala149ProfsTer4
XM_011525093.1:c.444del	XP_011523395.1:p.Ala149ProfsTer4
XM_011525094.1:c.444del	XP_011523396.1:p.Ala149ProfsTer4
XR_934513.1:n.1013del
XR_934514.1:n.1013del
XM_006722001.4:c.795del	XP_006722064.1:p.Ala266ProfsTer4
XM_006722002.4:c.795del	XP_006722065.1:p.Ala266ProfsTer4
XM_006722004.3:c.444del	XP_006722067.1:p.Ala149ProfsTer4
XM_006722005.3:c.444del	XP_006722068.1:p.Ala149ProfsTer4
XM_011525092.2:c.444del	XP_011523394.1:p.Ala149ProfsTer4
XM_011525093.2:c.444del	XP_011523395.1:p.Ala149ProfsTer4
XM_011525094.2:c.444del	XP_011523396.1:p.Ala149ProfsTer4
XM_017024914.1:c.444del	XP_016880403.1:p.Ala149ProfsTer4
XM_017024915.1:c.444del	XP_016880404.1:p.Ala149ProfsTer4
XM_017024916.1:c.444del	XP_016880405.1:p.Ala149ProfsTer4
XM_017024917.1:c.444del	XP_016880406.1:p.Ala149ProfsTer4
XM_017024918.2:c.444del	XP_016880407.1:p.Ala149ProfsTer4
XM_017024919.1:c.444del	XP_016880408.1:p.Ala149ProfsTer4
XR_934513.3:n.1444del
XR_934514.3:n.1444del
NM_058216.3:c.795del MANE Select	NP_478123.1:p.Ala266ProfsTer4
NR_103872.2:n.670del