Canonical Allele Identifier: CA3057229301
Community Standard Title: NM_058216.3(RAD51C):c.401_403del (p.Leu134del)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58695186_58695188del , CM000679.2:g.58695186_58695188del GRCh38
NC_000017.10:g.56772547_56772549del , CM000679.1:g.56772547_56772549del GRCh37
NC_000017.9:g.54127546_54127548del NCBI36
NG_023199.1:g.7585_7587del , LRG_314:g.7585_7587del
NG_047169.1:g.1894_1896del

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.401_403del MANE Select NP_478123.1:p.Leu134del
ENST00000337432.9:c.401_403del MANE Select ENSP00000336701.4:p.Leu134del
NM_002876.3:c.401_403del NP_002867.1:p.Leu134del
NM_002876.4:c.401_403del NP_002867.1:p.Leu134del
NM_058216.2:c.401_403del NP_478123.1:p.Leu134del
NR_103872.1:n.472_474del
NR_103872.2:n.443_445del
NR_103873.1:n.369_371del
ENST00000337432.8:c.401_403del ENSP00000336701.4:p.Leu134del
ENST00000413590.5:c.39_41del
ENST00000421782.3:c.401_403del ENSP00000391450.2:p.Leu134del
ENST00000425173.5:c.197_199del ENSP00000407282.1:p.Leu66del
ENST00000461271.5:c.50_52del ENSP00000464056.1:p.Leu17del
ENST00000461271.6:c.50_52del ENSP00000464056.2:p.Leu17del
ENST00000475762.5:c.*1104_*1106del ENSP00000432421.1:n.*1104_*1106del
ENST00000482007.5:c.401_403del ENSP00000433332.1:p.Leu134Ter
ENST00000486827.1:c.*1265_*1267del ENSP00000436761.1:n.*1265_*1267del
ENST00000487525.5:c.401_403del ENSP00000431637.1:p.Leu134Ter
ENST00000487921.5:n.313_315del
ENST00000583539.5:c.401_403del ENSP00000463121.1:p.Leu134del
ENST00000584617.5:c.127-1507_127-1505del
ENST00000622327.4:c.137_139del ENSP00000482326.1:p.Leu46del
ENST00000697675.1:n.1495_1497del
ENST00000697676.1:n.461_463del
ENST00000697677.1:n.1482_1484del
ENST00000697678.1:n.303_305del
ENST00000697679.1:n.1475_1477del
ENST00000697680.1:c.*1265_*1267del ENSP00000513392.1:n.*1265_*1267del
ENST00000697681.1:c.*1265_*1267del ENSP00000513393.1:n.*1265_*1267del
ENST00000697683.1:c.*1265_*1267del ENSP00000513395.1:n.*1265_*1267del
ENST00000697684.1:n.461_463del
ENST00000697685.1:c.*1265_*1267del ENSP00000513396.1:n.*1265_*1267del
ENST00000697686.1:c.50_52del ENSP00000513397.1:p.Leu17del
ENST00000697687.1:n.447_449del
ENST00000697688.1:n.447_449del
ENST00000697689.1:c.*1104_*1106del ENSP00000513398.1:n.*1104_*1106del
ENST00000697690.1:c.401_403del ENSP00000513399.1:p.Leu134del
ENST00000697691.1:c.*373_*375del ENSP00000513400.1:n.*373_*375del
ENST00000697692.1:c.*413_*415del ENSP00000513401.1:n.*413_*415del
ENST00000697693.1:n.1176_1178del
ENST00000697694.1:c.50_52del ENSP00000513402.1:p.Leu17del
ENST00000697695.1:n.1008_1010del
XM_006722001.2:c.401_403del XP_006722064.1:p.Leu134del
XM_006722001.4:c.401_403del XP_006722064.1:p.Leu134del
XM_006722002.2:c.401_403del XP_006722065.1:p.Leu134del
XM_006722002.4:c.401_403del XP_006722065.1:p.Leu134del
XM_006722004.2:c.50_52del XP_006722067.1:p.Leu17del
XM_006722004.3:c.50_52del XP_006722067.1:p.Leu17del
XM_006722005.2:c.50_52del XP_006722068.1:p.Leu17del
XM_006722005.3:c.50_52del XP_006722068.1:p.Leu17del
XM_011525092.1:c.50_52del XP_011523394.1:p.Leu17del
XM_011525092.2:c.50_52del XP_011523394.1:p.Leu17del
XM_011525093.1:c.50_52del XP_011523395.1:p.Leu17del
XM_011525093.2:c.50_52del XP_011523395.1:p.Leu17del
XM_011525094.1:c.50_52del XP_011523396.1:p.Leu17del
XM_011525094.2:c.50_52del XP_011523396.1:p.Leu17del
XM_017024914.1:c.50_52del XP_016880403.1:p.Leu17del
XM_017024915.1:c.50_52del XP_016880404.1:p.Leu17del
XM_017024916.1:c.50_52del XP_016880405.1:p.Leu17del
XM_017024917.1:c.50_52del XP_016880406.1:p.Leu17del
XM_017024918.2:c.50_52del XP_016880407.1:p.Leu17del
XM_017024919.1:c.50_52del XP_016880408.1:p.Leu17del
XR_934513.1:n.474_476del
XR_934513.3:n.905_907del
XR_934514.1:n.474_476del
XR_934514.3:n.905_907del