Canonical Allele Identifier: CA2733811759
Gene: RAD51C HGNC NCBI

Linked Data

dbSNP Id: rs2143796902

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703213del , CM000679.2:g.58703213del GRCh38
NC_000017.10:g.56780574del , CM000679.1:g.56780574del GRCh37
NC_000017.9:g.54135573del NCBI36
NG_023199.1:g.15612del , LRG_314:g.15612del

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.238del ENSP00000464056.2:p.Glu80ArgfsTer?
ENST00000697677.1:n.1670del
ENST00000697678.1:n.491del
ENST00000697679.1:n.1663del
ENST00000697680.1:c.*1453del ENSP00000513392.1:n.*1453del
ENST00000697681.1:c.*1605del ENSP00000513393.1:n.*1605del
ENST00000697683.1:c.*1453del ENSP00000513395.1:n.*1453del
ENST00000697684.1:n.649del
ENST00000697685.1:c.*1286del ENSP00000513396.1:n.*1286del
ENST00000697686.1:c.238del ENSP00000513397.1:p.Glu80ArgfsTer?
ENST00000697687.1:n.468del
ENST00000697688.1:n.635del
ENST00000697689.1:c.*1125del ENSP00000513398.1:n.*1125del
ENST00000697690.1:c.589del ENSP00000513399.1:p.Glu197ArgfsTer?
ENST00000697691.1:c.*561del ENSP00000513400.1:n.*561del
ENST00000697692.1:c.*601del ENSP00000513401.1:n.*601del
ENST00000697694.1:c.238del ENSP00000513402.1:p.Glu80ArgfsTer?
ENST00000697695.1:n.1196del
ENST00000337432.9:c.589del MANE Select ENSP00000336701.4:p.Glu197ArgfsTer?
ENST00000337432.8:c.589del ENSP00000336701.4:p.Glu197ArgfsTer?
ENST00000413590.5:c.227del
ENST00000425173.5:c.385del ENSP00000407282.1:p.Glu129ArgfsTer?
ENST00000461271.5:c.238del ENSP00000464056.1:p.Glu80ArgfsTer?
ENST00000475762.5:c.*1292del ENSP00000432421.1:n.*1292del
ENST00000482007.5:c.*17del ENSP00000433332.1:n.*17del
ENST00000487525.5:c.*17del ENSP00000431637.1:n.*17del
ENST00000487921.5:n.501del
ENST00000583539.5:c.589del ENSP00000463121.1:p.Glu197ArgfsTer?
ENST00000584617.5:c.311del
NM_058216.2:c.589del NP_478123.1:p.Glu197ArgfsTer?
NR_103872.1:n.493del
XM_006722001.2:c.589del XP_006722064.1:p.Glu197ArgfsTer?
XM_006722002.2:c.589del XP_006722065.1:p.Glu197ArgfsTer?
XM_006722004.2:c.238del XP_006722067.1:p.Glu80ArgfsTer?
XM_006722005.2:c.238del XP_006722068.1:p.Glu80ArgfsTer?
XM_011525092.1:c.238del XP_011523394.1:p.Glu80ArgfsTer?
XM_011525093.1:c.238del XP_011523395.1:p.Glu80ArgfsTer?
XM_011525094.1:c.238del XP_011523396.1:p.Glu80ArgfsTer?
XR_934513.1:n.662del
XR_934514.1:n.662del
XM_006722001.4:c.589del XP_006722064.1:p.Glu197ArgfsTer?
XM_006722002.4:c.589del XP_006722065.1:p.Glu197ArgfsTer?
XM_006722004.3:c.238del XP_006722067.1:p.Glu80ArgfsTer?
XM_006722005.3:c.238del XP_006722068.1:p.Glu80ArgfsTer?
XM_011525092.2:c.238del XP_011523394.1:p.Glu80ArgfsTer?
XM_011525093.2:c.238del XP_011523395.1:p.Glu80ArgfsTer?
XM_011525094.2:c.238del XP_011523396.1:p.Glu80ArgfsTer?
XM_017024914.1:c.238del XP_016880403.1:p.Glu80ArgfsTer?
XM_017024915.1:c.238del XP_016880404.1:p.Glu80ArgfsTer?
XM_017024916.1:c.238del XP_016880405.1:p.Glu80ArgfsTer?
XM_017024917.1:c.238del XP_016880406.1:p.Glu80ArgfsTer?
XM_017024918.2:c.238del XP_016880407.1:p.Glu80ArgfsTer?
XM_017024919.1:c.238del XP_016880408.1:p.Glu80ArgfsTer?
XR_934513.3:n.1093del
XR_934514.3:n.1093del
NM_058216.3:c.589del MANE Select NP_478123.1:p.Glu197ArgfsTer?
NR_103872.2:n.464del