Canonical Allele Identifier: CA16615476
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58720759_58720762del , CM000679.2:g.58720759_58720762del GRCh38
NC_000017.10:g.56798120_56798123del , CM000679.1:g.56798120_56798123del GRCh37
NC_000017.9:g.54153119_54153122del NCBI36
NG_023199.1:g.33158_33161del , LRG_314:g.33158_33161del

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.500_503del ENSP00000464056.2:p.Asn167ArgfsTer2
ENST00000697678.1:n.753_756del
ENST00000697679.1:n.1925_1928del
ENST00000697680.1:c.*1815_*1818del ENSP00000513392.1:n.*1815_*1818del
ENST00000697681.1:c.*2012_*2015del ENSP00000513393.1:n.*2012_*2015del
ENST00000697683.1:c.*1715_*1718del ENSP00000513395.1:n.*1715_*1718del
ENST00000697684.1:n.911_914del
ENST00000697685.1:c.*1548_*1551del ENSP00000513396.1:n.*1548_*1551del
ENST00000697686.1:c.500_503del ENSP00000513397.1:p.Asn167ArgfsTer2
ENST00000697687.1:n.730_733del
ENST00000697688.1:n.897_900del
ENST00000697689.1:c.*1387_*1390del ENSP00000513398.1:n.*1387_*1390del
ENST00000697690.1:c.851_854del ENSP00000513399.1:p.Asn284ArgfsTer2
ENST00000697691.1:c.*823_*826del ENSP00000513400.1:n.*823_*826del
ENST00000697692.1:c.*863_*866del ENSP00000513401.1:n.*863_*866del
ENST00000697694.1:c.500_503del ENSP00000513402.1:p.Asn167ArgfsTer2
ENST00000697695.1:n.1458_1461del
ENST00000337432.9:c.851_854del MANE Select ENSP00000336701.4:p.Asn284ArgfsTer2
ENST00000337432.8:c.851_854del ENSP00000336701.4:p.Asn284ArgfsTer2
ENST00000413590.5:c.489_492del
ENST00000475762.5:c.*1541-3281_*1541-3278del ENSP00000432421.1:n.*1541-3281_*1541-3278del
ENST00000482007.5:c.*279_*282del ENSP00000433332.1:n.*279_*282del
ENST00000487525.5:c.*424_*427del ENSP00000431637.1:n.*424_*427del
ENST00000578151.1:n.186_189del
ENST00000581221.5:n.366_369del
ENST00000583539.5:c.851_854del ENSP00000463121.1:p.Asn284ArgfsTer2
ENST00000584617.5:c.573_576del
ENST00000584804.1:c.146_149del ENSP00000463658.1:p.Asn49ArgfsTer2
NM_058216.2:c.851_854del NP_478123.1:p.Asn284ArgfsTer2
NR_103872.1:n.755_758del
XM_006722001.2:c.851_854del XP_006722064.1:p.Asn284ArgfsTer2
XM_006722002.2:c.851_854del XP_006722065.1:p.Asn284ArgfsTer2
XM_006722004.2:c.500_503del XP_006722067.1:p.Asn167ArgfsTer2
XM_006722005.2:c.500_503del XP_006722068.1:p.Asn167ArgfsTer2
XM_011525092.1:c.500_503del XP_011523394.1:p.Asn167ArgfsTer2
XM_011525093.1:c.500_503del XP_011523395.1:p.Asn167ArgfsTer2
XM_011525094.1:c.500_503del XP_011523396.1:p.Asn167ArgfsTer2
XR_934513.1:n.1069_1072del
XR_934514.1:n.1069_1072del
XM_006722001.4:c.851_854del XP_006722064.1:p.Asn284ArgfsTer2
XM_006722002.4:c.851_854del XP_006722065.1:p.Asn284ArgfsTer2
XM_006722004.3:c.500_503del XP_006722067.1:p.Asn167ArgfsTer2
XM_006722005.3:c.500_503del XP_006722068.1:p.Asn167ArgfsTer2
XM_011525092.2:c.500_503del XP_011523394.1:p.Asn167ArgfsTer2
XM_011525093.2:c.500_503del XP_011523395.1:p.Asn167ArgfsTer2
XM_011525094.2:c.500_503del XP_011523396.1:p.Asn167ArgfsTer2
XM_017024914.1:c.500_503del XP_016880403.1:p.Asn167ArgfsTer2
XM_017024915.1:c.500_503del XP_016880404.1:p.Asn167ArgfsTer2
XM_017024916.1:c.500_503del XP_016880405.1:p.Asn167ArgfsTer2
XM_017024917.1:c.500_503del XP_016880406.1:p.Asn167ArgfsTer2
XM_017024918.2:c.500_503del XP_016880407.1:p.Asn167ArgfsTer2
XM_017024919.1:c.500_503del XP_016880408.1:p.Asn167ArgfsTer2
XR_934513.3:n.1500_1503del
XR_934514.3:n.1500_1503del
NM_058216.3:c.851_854del MANE Select NP_478123.1:p.Asn284ArgfsTer2
NR_103872.2:n.726_729del