Canonical Allele Identifier: CA3057242607
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709862del , CM000679.2:g.58709862del GRCh38
NC_000017.10:g.56787223del , CM000679.1:g.56787223del GRCh37
NC_000017.9:g.54142222del NCBI36
NG_023199.1:g.22261del , LRG_314:g.22261del

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.358del ENSP00000464056.2:p.Arg120AspfsTer2
ENST00000697678.1:n.611del
ENST00000697679.1:n.1783del
ENST00000697680.1:c.*1573del ENSP00000513392.1:n.*1573del
ENST00000697681.1:c.*1870del ENSP00000513393.1:n.*1870del
ENST00000697683.1:c.*1573del ENSP00000513395.1:n.*1573del
ENST00000697684.1:n.769del
ENST00000697685.1:c.*1406del ENSP00000513396.1:n.*1406del
ENST00000697686.1:c.358del ENSP00000513397.1:p.Arg120AspfsTer2
ENST00000697687.1:n.588del
ENST00000697688.1:n.755del
ENST00000697689.1:c.*1245del ENSP00000513398.1:n.*1245del
ENST00000697690.1:c.709del ENSP00000513399.1:p.Arg237AspfsTer2
ENST00000697691.1:c.*681del ENSP00000513400.1:n.*681del
ENST00000697692.1:c.*721del ENSP00000513401.1:n.*721del
ENST00000697694.1:c.358del ENSP00000513402.1:p.Arg120AspfsTer2
ENST00000697695.1:n.1316del
ENST00000337432.9:c.709del MANE Select ENSP00000336701.4:p.Arg237AspfsTer2
ENST00000337432.8:c.709del ENSP00000336701.4:p.Arg237AspfsTer2
ENST00000413590.5:c.347del
ENST00000425173.5:c.625del ENSP00000407282.1:p.Arg209AspfsTer2
ENST00000461271.5:c.358del ENSP00000464056.1:p.Arg120AspfsTer2
ENST00000475762.5:c.*1412del ENSP00000432421.1:n.*1412del
ENST00000482007.5:c.*137del ENSP00000433332.1:n.*137del
ENST00000487525.5:c.*282del ENSP00000431637.1:n.*282del
ENST00000578151.1:n.44del
ENST00000581221.5:n.224del
ENST00000583539.5:c.709del ENSP00000463121.1:p.Arg237AspfsTer2
ENST00000584617.5:c.431del
ENST00000584804.1:c.4del ENSP00000463658.1:p.Arg2AspfsTer2
NM_058216.2:c.709del NP_478123.1:p.Arg237AspfsTer2
NR_103872.1:n.613del
XM_006722001.2:c.709del XP_006722064.1:p.Arg237AspfsTer2
XM_006722002.2:c.709del XP_006722065.1:p.Arg237AspfsTer2
XM_006722004.2:c.358del XP_006722067.1:p.Arg120AspfsTer2
XM_006722005.2:c.358del XP_006722068.1:p.Arg120AspfsTer2
XM_011525092.1:c.358del XP_011523394.1:p.Arg120AspfsTer2
XM_011525093.1:c.358del XP_011523395.1:p.Arg120AspfsTer2
XM_011525094.1:c.358del XP_011523396.1:p.Arg120AspfsTer2
XR_934513.1:n.927del
XR_934514.1:n.927del
XM_006722001.4:c.709del XP_006722064.1:p.Arg237AspfsTer2
XM_006722002.4:c.709del XP_006722065.1:p.Arg237AspfsTer2
XM_006722004.3:c.358del XP_006722067.1:p.Arg120AspfsTer2
XM_006722005.3:c.358del XP_006722068.1:p.Arg120AspfsTer2
XM_011525092.2:c.358del XP_011523394.1:p.Arg120AspfsTer2
XM_011525093.2:c.358del XP_011523395.1:p.Arg120AspfsTer2
XM_011525094.2:c.358del XP_011523396.1:p.Arg120AspfsTer2
XM_017024914.1:c.358del XP_016880403.1:p.Arg120AspfsTer2
XM_017024915.1:c.358del XP_016880404.1:p.Arg120AspfsTer2
XM_017024916.1:c.358del XP_016880405.1:p.Arg120AspfsTer2
XM_017024917.1:c.358del XP_016880406.1:p.Arg120AspfsTer2
XM_017024918.2:c.358del XP_016880407.1:p.Arg120AspfsTer2
XM_017024919.1:c.358del XP_016880408.1:p.Arg120AspfsTer2
XR_934513.3:n.1358del
XR_934514.3:n.1358del
NM_058216.3:c.709del MANE Select NP_478123.1:p.Arg237AspfsTer2
NR_103872.2:n.584del