Canonical Allele Identifier: CA169339
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 142758
dbSNP Id: rs587782699

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58696789_58696790dup , CM000679.2:g.58696789_58696790dup GRCh38
NC_000017.10:g.56774150_56774151dup , CM000679.1:g.56774150_56774151dup GRCh37
NC_000017.9:g.54129149_54129150dup NCBI36
NG_023199.1:g.9188_9189dup , LRG_314:g.9188_9189dup
NG_047169.1:g.291_292dup

Transcript Alleles

HGVS Amino-acid change
ENST00000461271.6:c.150_151dup ENSP00000464056.2:p.Arg51IlefsTer4
ENST00000697675.1:n.3098_3099dup
ENST00000697676.1:n.561_562dup
ENST00000697677.1:n.1582_1583dup
ENST00000697678.1:n.403_404dup
ENST00000697679.1:n.1575_1576dup
ENST00000697680.1:c.*1365_*1366dup ENSP00000513392.1:n.*1365_*1366dup
ENST00000697681.1:c.*1392_*1393dup ENSP00000513393.1:n.*1392_*1393dup
ENST00000697683.1:c.*1365_*1366dup ENSP00000513395.1:n.*1365_*1366dup
ENST00000697684.1:n.561_562dup
ENST00000697685.1:c.*1268+1600_*1268+1601dup ENSP00000513396.1:n.*1268+1600_*1268+1601...
ENST00000697686.1:c.150_151dup ENSP00000513397.1:p.Arg51IlefsTer4
ENST00000697687.1:n.450+1600_450+1601dup
ENST00000697688.1:n.547_548dup
ENST00000697689.1:c.*1107+1600_*1107+1601dup ENSP00000513398.1:n.*1107+1600_*1107+1601...
ENST00000697690.1:c.501_502dup ENSP00000513399.1:p.Arg168IlefsTer4
ENST00000697691.1:c.*473_*474dup ENSP00000513400.1:n.*473_*474dup
ENST00000697692.1:c.*513_*514dup ENSP00000513401.1:n.*513_*514dup
ENST00000697694.1:c.150_151dup ENSP00000513402.1:p.Arg51IlefsTer4
ENST00000697695.1:n.1108_1109dup
ENST00000337432.9:c.501_502dup MANE Select ENSP00000336701.4:p.Arg168IlefsTer4
ENST00000337432.8:c.501_502dup ENSP00000336701.4:p.Arg168IlefsTer4
ENST00000413590.5:c.139_140dup
ENST00000425173.5:c.297_298dup ENSP00000407282.1:p.Arg100IlefsTer4
ENST00000461271.5:c.150_151dup ENSP00000464056.1:p.Arg51IlefsTer4
ENST00000475762.5:c.*1204_*1205dup ENSP00000432421.1:n.*1204_*1205dup
ENST00000482007.5:c.404+1600_404+1601dup ENSP00000433332.1:n.404+1600_404+1601dup
ENST00000487525.5:c.404+1600_404+1601dup ENSP00000431637.1:n.404+1600_404+1601dup
ENST00000487921.5:n.413_414dup
ENST00000583539.5:c.501_502dup ENSP00000463121.1:p.Arg168IlefsTer4
ENST00000584617.5:c.223_224dup
ENST00000622327.4:c.237_238dup ENSP00000482326.1:p.Arg80IlefsTer4
NM_058216.2:c.501_502dup NP_478123.1:p.Arg168IlefsTer4
NR_103872.1:n.475+1600_475+1601dup
XM_006722001.2:c.501_502dup XP_006722064.1:p.Arg168IlefsTer4
XM_006722002.2:c.501_502dup XP_006722065.1:p.Arg168IlefsTer4
XM_006722004.2:c.150_151dup XP_006722067.1:p.Arg51IlefsTer4
XM_006722005.2:c.150_151dup XP_006722068.1:p.Arg51IlefsTer4
XM_011525092.1:c.150_151dup XP_011523394.1:p.Arg51IlefsTer4
XM_011525093.1:c.150_151dup XP_011523395.1:p.Arg51IlefsTer4
XM_011525094.1:c.150_151dup XP_011523396.1:p.Arg51IlefsTer4
XR_934513.1:n.574_575dup
XR_934514.1:n.574_575dup
XM_006722001.4:c.501_502dup XP_006722064.1:p.Arg168IlefsTer4
XM_006722002.4:c.501_502dup XP_006722065.1:p.Arg168IlefsTer4
XM_006722004.3:c.150_151dup XP_006722067.1:p.Arg51IlefsTer4
XM_006722005.3:c.150_151dup XP_006722068.1:p.Arg51IlefsTer4
XM_011525092.2:c.150_151dup XP_011523394.1:p.Arg51IlefsTer4
XM_011525093.2:c.150_151dup XP_011523395.1:p.Arg51IlefsTer4
XM_011525094.2:c.150_151dup XP_011523396.1:p.Arg51IlefsTer4
XM_017024914.1:c.150_151dup XP_016880403.1:p.Arg51IlefsTer4
XM_017024915.1:c.150_151dup XP_016880404.1:p.Arg51IlefsTer4
XM_017024916.1:c.150_151dup XP_016880405.1:p.Arg51IlefsTer4
XM_017024917.1:c.150_151dup XP_016880406.1:p.Arg51IlefsTer4
XM_017024918.2:c.150_151dup XP_016880407.1:p.Arg51IlefsTer4
XM_017024919.1:c.150_151dup XP_016880408.1:p.Arg51IlefsTer4
XR_934513.3:n.1005_1006dup
XR_934514.3:n.1005_1006dup
NM_058216.3:c.501_502dup MANE Select NP_478123.1:p.Arg168IlefsTer4
NR_103872.2:n.446+1600_446+1601dup