Canonical Allele Identifier: CA16620490
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 422429
dbSNP Id: rs1064795774

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58695010del , CM000679.2:g.58695010del GRCh38
NC_000017.10:g.56772371del , CM000679.1:g.56772371del GRCh37
NC_000017.9:g.54127370del NCBI36
NG_023199.1:g.7409del , LRG_314:g.7409del
NG_047169.1:g.2070del

Transcript Alleles

HGVS Amino-acid change
ENST00000461271.6:c.-127del ENSP00000464056.2:n.-127del
ENST00000697675.1:n.1319del
ENST00000697676.1:n.285del
ENST00000697677.1:n.1306del
ENST00000697678.1:n.127del
ENST00000697679.1:n.1299del
ENST00000697680.1:c.*1089del ENSP00000513392.1:n.*1089del
ENST00000697681.1:c.*1089del ENSP00000513393.1:n.*1089del
ENST00000697683.1:c.*1089del ENSP00000513395.1:n.*1089del
ENST00000697684.1:n.285del
ENST00000697685.1:c.*1089del ENSP00000513396.1:n.*1089del
ENST00000697686.1:c.-127del ENSP00000513397.1:n.-127del
ENST00000697687.1:n.271del
ENST00000697688.1:n.271del
ENST00000697689.1:c.*928del ENSP00000513398.1:n.*928del
ENST00000697690.1:c.225del ENSP00000513399.1:p.Tyr75Ter
ENST00000697691.1:c.*197del ENSP00000513400.1:n.*197del
ENST00000697692.1:c.*237del ENSP00000513401.1:n.*237del
ENST00000697693.1:n.1000del
ENST00000697694.1:c.-127del ENSP00000513402.1:n.-127del
ENST00000697695.1:n.832del
ENST00000337432.9:c.225del MANE Select ENSP00000336701.4:p.Tyr75Ter
ENST00000337432.8:c.225del ENSP00000336701.4:p.Tyr75Ter
ENST00000421782.3:c.225del ENSP00000391450.2:p.Tyr75Ter
ENST00000425173.5:c.21del ENSP00000407282.1:p.Tyr7Ter
ENST00000461271.5:c.-127del ENSP00000464056.1:n.-127del
ENST00000475762.5:c.*928del ENSP00000432421.1:n.*928del
ENST00000482007.5:c.225del ENSP00000433332.1:p.Tyr75Ter
ENST00000486827.1:c.*1089del ENSP00000436761.1:n.*1089del
ENST00000487525.5:c.225del ENSP00000431637.1:p.Tyr75Ter
ENST00000487921.5:n.137del
ENST00000583539.5:c.225del ENSP00000463121.1:p.Tyr75Ter
ENST00000584617.5:c.127-1683del
NM_002876.3:c.225del NP_002867.1:p.Tyr75Ter
NM_058216.2:c.225del NP_478123.1:p.Tyr75Ter
NR_103872.1:n.296del
NR_103873.1:n.193del
XM_006722001.2:c.225del XP_006722064.1:p.Tyr75Ter
XM_006722002.2:c.225del XP_006722065.1:p.Tyr75Ter
XM_006722004.2:c.-127del XP_006722067.1:n.-127del
XM_006722005.2:c.-127del XP_006722068.1:n.-127del
XM_011525092.1:c.-127del XP_011523394.1:n.-127del
XM_011525093.1:c.-127del XP_011523395.1:n.-127del
XM_011525094.1:c.-127del XP_011523396.1:n.-127del
XR_934513.1:n.298del
XR_934514.1:n.298del
XM_006722001.4:c.225del XP_006722064.1:p.Tyr75Ter
XM_006722002.4:c.225del XP_006722065.1:p.Tyr75Ter
XM_006722004.3:c.-127del XP_006722067.1:n.-127del
XM_006722005.3:c.-127del XP_006722068.1:n.-127del
XM_011525092.2:c.-127del XP_011523394.1:n.-127del
XM_011525093.2:c.-127del XP_011523395.1:n.-127del
XM_011525094.2:c.-127del XP_011523396.1:n.-127del
XM_017024914.1:c.-127del XP_016880403.1:n.-127del
XM_017024915.1:c.-127del XP_016880404.1:n.-127del
XM_017024916.1:c.-127del XP_016880405.1:n.-127del
XM_017024917.1:c.-127del XP_016880406.1:n.-127del
XM_017024918.2:c.-127del XP_016880407.1:n.-127del
XM_017024919.1:c.-127del XP_016880408.1:n.-127del
XR_934513.3:n.729del
XR_934514.3:n.729del
NM_058216.3:c.225del MANE Select NP_478123.1:p.Tyr75Ter
NR_103872.2:n.267del
NM_002876.4:c.225del NP_002867.1:p.Tyr75Ter