Canonical Allele Identifier: CA16615755
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 409862
dbSNP Id: rs1064792966

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734148_58734157del , CM000679.2:g.58734148_58734157del GRCh38
NC_000017.10:g.56811509_56811518del , CM000679.1:g.56811509_56811518del GRCh37
NC_000017.9:g.54166508_54166517del NCBI36
NG_023199.1:g.46547_46556del , LRG_314:g.46547_46556del

Transcript Alleles

HGVS Amino-acid change
ENST00000461271.6:c.*1589_*1598del ENSP00000464056.2:n.*1589_*1598del
ENST00000697680.1:c.*2021_*2030del ENSP00000513392.1:n.*2021_*2030del
ENST00000697681.1:c.*2218_*2227del ENSP00000513393.1:n.*2218_*2227del
ENST00000697683.1:c.*1993_*2002del ENSP00000513395.1:n.*1993_*2002del
ENST00000697685.1:c.*1754_*1763del ENSP00000513396.1:n.*1754_*1763del
ENST00000697686.1:c.828_837del ENSP00000513397.1:p.Leu277IlefsTer?
ENST00000697689.1:c.*1471_*1480del ENSP00000513398.1:n.*1471_*1480del
ENST00000697690.1:c.*17_*26del ENSP00000513399.1:n.*17_*26del
ENST00000697691.1:c.*1029_*1038del ENSP00000513400.1:n.*1029_*1038del
ENST00000697692.1:c.*1069_*1078del ENSP00000513401.1:n.*1069_*1078del
ENST00000697694.1:c.706_715del ENSP00000513402.1:p.Ser236HisfsTer8
ENST00000697695.1:n.1664_1673del
ENST00000337432.9:c.1057_1066del MANE Select ENSP00000336701.4:p.Ser353HisfsTer8
ENST00000337432.8:c.1057_1066del ENSP00000336701.4:p.Ser353HisfsTer8
ENST00000413590.5:c.698_707del
ENST00000461706.1:n.244_253del
ENST00000475762.5:c.*1693_*1702del ENSP00000432421.1:n.*1693_*1702del
ENST00000482007.5:c.*485_*494del ENSP00000433332.1:n.*485_*494del
ENST00000487525.5:c.*633_*642del ENSP00000431637.1:n.*633_*642del
ENST00000578151.1:n.270_279del
ENST00000581221.5:n.572_581del
ENST00000584804.1:c.291_300del ENSP00000463658.1:p.Leu98IlefsTer?
NM_058216.2:c.1057_1066del NP_478123.1:p.Ser353HisfsTer8
NR_103872.1:n.961_970del
XM_006722001.2:c.1060_1069del XP_006722064.1:p.Ser354HisfsTer8
XM_006722002.2:c.996_1005del XP_006722065.1:p.Leu333IlefsTer?
XM_006722004.2:c.709_718del XP_006722067.1:p.Ser237HisfsTer8
XM_006722005.2:c.709_718del XP_006722068.1:p.Ser237HisfsTer8
XM_011525092.1:c.709_718del XP_011523394.1:p.Ser237HisfsTer8
XM_011525093.1:c.709_718del XP_011523395.1:p.Ser237HisfsTer8
XM_011525094.1:c.709_718del XP_011523396.1:p.Ser237HisfsTer8
XR_934513.1:n.1275_1284del
XR_934514.1:n.1278_1287del
XR_934886.1:n.149+3915_149+3924del
XM_006722001.4:c.1060_1069del XP_006722064.1:p.Ser354HisfsTer8
XM_006722002.4:c.996_1005del XP_006722065.1:p.Leu333IlefsTer?
XM_006722004.3:c.709_718del XP_006722067.1:p.Ser237HisfsTer8
XM_006722005.3:c.709_718del XP_006722068.1:p.Ser237HisfsTer8
XM_011525092.2:c.709_718del XP_011523394.1:p.Ser237HisfsTer8
XM_011525093.2:c.709_718del XP_011523395.1:p.Ser237HisfsTer8
XM_011525094.2:c.709_718del XP_011523396.1:p.Ser237HisfsTer8
XM_017024914.1:c.706_715del XP_016880403.1:p.Ser236HisfsTer8
XM_017024915.1:c.706_715del XP_016880404.1:p.Ser236HisfsTer8
XM_017024916.1:c.706_715del XP_016880405.1:p.Ser236HisfsTer8
XM_017024917.1:c.706_715del XP_016880406.1:p.Ser236HisfsTer8
XM_017024918.2:c.706_715del XP_016880407.1:p.Ser236HisfsTer8
XM_017024919.1:c.645_654del XP_016880408.1:p.Leu216IlefsTer?
XR_934513.3:n.1706_1715del
XR_934514.3:n.1709_1718del
XR_934886.2:n.149+3915_149+3924del
NM_058216.3:c.1057_1066del MANE Select NP_478123.1:p.Ser353HisfsTer8
NR_103872.2:n.932_941del