Canonical Allele Identifier: CA2580094432

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 1746438
• ClinVar RCV Id: RCV002341019

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58696814_58696816delinsCCT , CM000679.2:g.58696814_58696816delinsCCT	GRCh38
NC_000017.10:g.56774175_56774177delinsCCT , CM000679.1:g.56774175_56774177delinsCCT	GRCh37
NC_000017.9:g.54129174_54129176delinsCCT	NCBI36
NG_023199.1:g.9213_9215delinsCCT , LRG_314:g.9213_9215delinsCCT
NG_047169.1:g.264_266delinsAGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.175_177delinsCCT	ENSP00000464056.2:p.Cys59Pro
ENST00000697675.1:n.3123_3125delinsCCT
ENST00000697676.1:n.586_588delinsCCT
ENST00000697677.1:n.1607_1609delinsCCT
ENST00000697678.1:n.428_430delinsCCT
ENST00000697679.1:n.1600_1602delinsCCT
ENST00000697680.1:c.*1390_*1392delinsCCT	ENSP00000513392.1:n.*1390_*1392delinsCCT
ENST00000697681.1:c.*1417_*1419delinsCCT	ENSP00000513393.1:n.*1417_*1419delinsCCT
ENST00000697683.1:c.*1390_*1392delinsCCT	ENSP00000513395.1:n.*1390_*1392delinsCCT
ENST00000697684.1:n.586_588delinsCCT
ENST00000697685.1:c.*1268+1625_*1268+1627delinsCCT	ENSP00000513396.1:n.*1268+1625_*1268+1627...
ENST00000697686.1:c.175_177delinsCCT	ENSP00000513397.1:p.Cys59Pro
ENST00000697687.1:n.450+1625_450+1627delinsCCT
ENST00000697688.1:n.572_574delinsCCT
ENST00000697689.1:c.*1107+1625_*1107+1627delinsCCT	ENSP00000513398.1:n.*1107+1625_*1107+1627...
ENST00000697690.1:c.526_528delinsCCT	ENSP00000513399.1:p.Cys176Pro
ENST00000697691.1:c.*498_*500delinsCCT	ENSP00000513400.1:n.*498_*500delinsCCT
ENST00000697692.1:c.*538_*540delinsCCT	ENSP00000513401.1:n.*538_*540delinsCCT
ENST00000697694.1:c.175_177delinsCCT	ENSP00000513402.1:p.Cys59Pro
ENST00000697695.1:n.1133_1135delinsCCT
ENST00000337432.9:c.526_528delinsCCT MANE Select	ENSP00000336701.4:p.Cys176Pro
ENST00000337432.8:c.526_528delinsCCT	ENSP00000336701.4:p.Cys176Pro
ENST00000413590.5:c.164_166delinsCCT
ENST00000425173.5:c.322_324delinsCCT	ENSP00000407282.1:p.Cys108Pro
ENST00000461271.5:c.175_177delinsCCT	ENSP00000464056.1:p.Cys59Pro
ENST00000475762.5:c.*1229_*1231delinsCCT	ENSP00000432421.1:n.*1229_*1231delinsCCT
ENST00000482007.5:c.404+1625_404+1627delinsCCT	ENSP00000433332.1:n.404+1625_404+1627deli...
ENST00000487525.5:c.404+1625_404+1627delinsCCT	ENSP00000431637.1:n.404+1625_404+1627deli...
ENST00000487921.5:n.438_440delinsCCT
ENST00000583539.5:c.526_528delinsCCT	ENSP00000463121.1:p.Cys176Pro
ENST00000584617.5:c.248_250delinsCCT
ENST00000622327.4:c.262_264delinsCCT	ENSP00000482326.1:p.Cys88Pro
NM_058216.2:c.526_528delinsCCT	NP_478123.1:p.Cys176Pro
NR_103872.1:n.475+1625_475+1627delinsCCT
XM_006722001.2:c.526_528delinsCCT	XP_006722064.1:p.Cys176Pro
XM_006722002.2:c.526_528delinsCCT	XP_006722065.1:p.Cys176Pro
XM_006722004.2:c.175_177delinsCCT	XP_006722067.1:p.Cys59Pro
XM_006722005.2:c.175_177delinsCCT	XP_006722068.1:p.Cys59Pro
XM_011525092.1:c.175_177delinsCCT	XP_011523394.1:p.Cys59Pro
XM_011525093.1:c.175_177delinsCCT	XP_011523395.1:p.Cys59Pro
XM_011525094.1:c.175_177delinsCCT	XP_011523396.1:p.Cys59Pro
XR_934513.1:n.599_601delinsCCT
XR_934514.1:n.599_601delinsCCT
XM_006722001.4:c.526_528delinsCCT	XP_006722064.1:p.Cys176Pro
XM_006722002.4:c.526_528delinsCCT	XP_006722065.1:p.Cys176Pro
XM_006722004.3:c.175_177delinsCCT	XP_006722067.1:p.Cys59Pro
XM_006722005.3:c.175_177delinsCCT	XP_006722068.1:p.Cys59Pro
XM_011525092.2:c.175_177delinsCCT	XP_011523394.1:p.Cys59Pro
XM_011525093.2:c.175_177delinsCCT	XP_011523395.1:p.Cys59Pro
XM_011525094.2:c.175_177delinsCCT	XP_011523396.1:p.Cys59Pro
XM_017024914.1:c.175_177delinsCCT	XP_016880403.1:p.Cys59Pro
XM_017024915.1:c.175_177delinsCCT	XP_016880404.1:p.Cys59Pro
XM_017024916.1:c.175_177delinsCCT	XP_016880405.1:p.Cys59Pro
XM_017024917.1:c.175_177delinsCCT	XP_016880406.1:p.Cys59Pro
XM_017024918.2:c.175_177delinsCCT	XP_016880407.1:p.Cys59Pro
XM_017024919.1:c.175_177delinsCCT	XP_016880408.1:p.Cys59Pro
XR_934513.3:n.1030_1032delinsCCT
XR_934514.3:n.1030_1032delinsCCT
NM_058216.3:c.526_528delinsCCT MANE Select	NP_478123.1:p.Cys176Pro
NR_103872.2:n.446+1625_446+1627delinsCCT