Canonical Allele Identifier: CA3057242647
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709928del , CM000679.2:g.58709928del GRCh38
NC_000017.10:g.56787289del , CM000679.1:g.56787289del GRCh37
NC_000017.9:g.54142288del NCBI36
NG_023199.1:g.22327del , LRG_314:g.22327del

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.424del ENSP00000464056.2:p.Thr142LeufsTer4
ENST00000697678.1:n.677del
ENST00000697679.1:n.1849del
ENST00000697680.1:c.*1639del ENSP00000513392.1:n.*1639del
ENST00000697681.1:c.*1936del ENSP00000513393.1:n.*1936del
ENST00000697683.1:c.*1639del ENSP00000513395.1:n.*1639del
ENST00000697684.1:n.835del
ENST00000697685.1:c.*1472del ENSP00000513396.1:n.*1472del
ENST00000697686.1:c.424del ENSP00000513397.1:p.Thr142LeufsTer4
ENST00000697687.1:n.654del
ENST00000697688.1:n.821del
ENST00000697689.1:c.*1311del ENSP00000513398.1:n.*1311del
ENST00000697690.1:c.775del ENSP00000513399.1:p.Thr259LeufsTer4
ENST00000697691.1:c.*747del ENSP00000513400.1:n.*747del
ENST00000697692.1:c.*787del ENSP00000513401.1:n.*787del
ENST00000697694.1:c.424del ENSP00000513402.1:p.Thr142LeufsTer4
ENST00000697695.1:n.1382del
ENST00000337432.9:c.775del MANE Select ENSP00000336701.4:p.Thr259LeufsTer4
ENST00000337432.8:c.775del ENSP00000336701.4:p.Thr259LeufsTer4
ENST00000413590.5:c.413del
ENST00000475762.5:c.*1478del ENSP00000432421.1:n.*1478del
ENST00000482007.5:c.*203del ENSP00000433332.1:n.*203del
ENST00000487525.5:c.*348del ENSP00000431637.1:n.*348del
ENST00000578151.1:n.110del
ENST00000581221.5:n.290del
ENST00000583539.5:c.775del ENSP00000463121.1:p.Thr259LeufsTer4
ENST00000584617.5:c.497del
ENST00000584804.1:c.70del ENSP00000463658.1:p.Thr24LeufsTer4
NM_058216.2:c.775del NP_478123.1:p.Thr259LeufsTer4
NR_103872.1:n.679del
XM_006722001.2:c.775del XP_006722064.1:p.Thr259LeufsTer4
XM_006722002.2:c.775del XP_006722065.1:p.Thr259LeufsTer4
XM_006722004.2:c.424del XP_006722067.1:p.Thr142LeufsTer4
XM_006722005.2:c.424del XP_006722068.1:p.Thr142LeufsTer4
XM_011525092.1:c.424del XP_011523394.1:p.Thr142LeufsTer4
XM_011525093.1:c.424del XP_011523395.1:p.Thr142LeufsTer4
XM_011525094.1:c.424del XP_011523396.1:p.Thr142LeufsTer4
XR_934513.1:n.993del
XR_934514.1:n.993del
XM_006722001.4:c.775del XP_006722064.1:p.Thr259LeufsTer4
XM_006722002.4:c.775del XP_006722065.1:p.Thr259LeufsTer4
XM_006722004.3:c.424del XP_006722067.1:p.Thr142LeufsTer4
XM_006722005.3:c.424del XP_006722068.1:p.Thr142LeufsTer4
XM_011525092.2:c.424del XP_011523394.1:p.Thr142LeufsTer4
XM_011525093.2:c.424del XP_011523395.1:p.Thr142LeufsTer4
XM_011525094.2:c.424del XP_011523396.1:p.Thr142LeufsTer4
XM_017024914.1:c.424del XP_016880403.1:p.Thr142LeufsTer4
XM_017024915.1:c.424del XP_016880404.1:p.Thr142LeufsTer4
XM_017024916.1:c.424del XP_016880405.1:p.Thr142LeufsTer4
XM_017024917.1:c.424del XP_016880406.1:p.Thr142LeufsTer4
XM_017024918.2:c.424del XP_016880407.1:p.Thr142LeufsTer4
XM_017024919.1:c.424del XP_016880408.1:p.Thr142LeufsTer4
XR_934513.3:n.1424del
XR_934514.3:n.1424del
NM_058216.3:c.775del MANE Select NP_478123.1:p.Thr259LeufsTer4
NR_103872.2:n.650del