Canonical Allele Identifier: CA3057242605
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709861del , CM000679.2:g.58709861del GRCh38
NC_000017.10:g.56787222del , CM000679.1:g.56787222del GRCh37
NC_000017.9:g.54142221del NCBI36
NG_023199.1:g.22260del , LRG_314:g.22260del

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.357del ENSP00000464056.2:p.Arg120AspfsTer2
ENST00000697678.1:n.610del
ENST00000697679.1:n.1782del
ENST00000697680.1:c.*1572del ENSP00000513392.1:n.*1572del
ENST00000697681.1:c.*1869del ENSP00000513393.1:n.*1869del
ENST00000697683.1:c.*1572del ENSP00000513395.1:n.*1572del
ENST00000697684.1:n.768del
ENST00000697685.1:c.*1405del ENSP00000513396.1:n.*1405del
ENST00000697686.1:c.357del ENSP00000513397.1:p.Arg120AspfsTer2
ENST00000697687.1:n.587del
ENST00000697688.1:n.754del
ENST00000697689.1:c.*1244del ENSP00000513398.1:n.*1244del
ENST00000697690.1:c.708del ENSP00000513399.1:p.Arg237AspfsTer2
ENST00000697691.1:c.*680del ENSP00000513400.1:n.*680del
ENST00000697692.1:c.*720del ENSP00000513401.1:n.*720del
ENST00000697694.1:c.357del ENSP00000513402.1:p.Arg120AspfsTer2
ENST00000697695.1:n.1315del
ENST00000337432.9:c.708del MANE Select ENSP00000336701.4:p.Arg237AspfsTer2
ENST00000337432.8:c.708del ENSP00000336701.4:p.Arg237AspfsTer2
ENST00000413590.5:c.346del
ENST00000425173.5:c.624del ENSP00000407282.1:p.Arg209AspfsTer2
ENST00000461271.5:c.357del ENSP00000464056.1:p.Arg120AspfsTer2
ENST00000475762.5:c.*1411del ENSP00000432421.1:n.*1411del
ENST00000482007.5:c.*136del ENSP00000433332.1:n.*136del
ENST00000487525.5:c.*281del ENSP00000431637.1:n.*281del
ENST00000578151.1:n.43del
ENST00000581221.5:n.223del
ENST00000583539.5:c.708del ENSP00000463121.1:p.Arg237AspfsTer2
ENST00000584617.5:c.430del
ENST00000584804.1:c.3del ENSP00000463658.1:p.Arg2AspfsTer2
NM_058216.2:c.708del NP_478123.1:p.Arg237AspfsTer2
NR_103872.1:n.612del
XM_006722001.2:c.708del XP_006722064.1:p.Arg237AspfsTer2
XM_006722002.2:c.708del XP_006722065.1:p.Arg237AspfsTer2
XM_006722004.2:c.357del XP_006722067.1:p.Arg120AspfsTer2
XM_006722005.2:c.357del XP_006722068.1:p.Arg120AspfsTer2
XM_011525092.1:c.357del XP_011523394.1:p.Arg120AspfsTer2
XM_011525093.1:c.357del XP_011523395.1:p.Arg120AspfsTer2
XM_011525094.1:c.357del XP_011523396.1:p.Arg120AspfsTer2
XR_934513.1:n.926del
XR_934514.1:n.926del
XM_006722001.4:c.708del XP_006722064.1:p.Arg237AspfsTer2
XM_006722002.4:c.708del XP_006722065.1:p.Arg237AspfsTer2
XM_006722004.3:c.357del XP_006722067.1:p.Arg120AspfsTer2
XM_006722005.3:c.357del XP_006722068.1:p.Arg120AspfsTer2
XM_011525092.2:c.357del XP_011523394.1:p.Arg120AspfsTer2
XM_011525093.2:c.357del XP_011523395.1:p.Arg120AspfsTer2
XM_011525094.2:c.357del XP_011523396.1:p.Arg120AspfsTer2
XM_017024914.1:c.357del XP_016880403.1:p.Arg120AspfsTer2
XM_017024915.1:c.357del XP_016880404.1:p.Arg120AspfsTer2
XM_017024916.1:c.357del XP_016880405.1:p.Arg120AspfsTer2
XM_017024917.1:c.357del XP_016880406.1:p.Arg120AspfsTer2
XM_017024918.2:c.357del XP_016880407.1:p.Arg120AspfsTer2
XM_017024919.1:c.357del XP_016880408.1:p.Arg120AspfsTer2
XR_934513.3:n.1357del
XR_934514.3:n.1357del
NM_058216.3:c.708del MANE Select NP_478123.1:p.Arg237AspfsTer2
NR_103872.2:n.583del