Canonical Allele Identifier: CA3261178714
Community Standard Title: NM_058216.3(RAD51C):c.710del (p.Arg237HisfsTer2)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709863del , CM000679.2:g.58709863del GRCh38
NC_000017.10:g.56787224del , CM000679.1:g.56787224del GRCh37
NC_000017.9:g.54142223del NCBI36
NG_023199.1:g.22262del , LRG_314:g.22262del

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.710del MANE Select NP_478123.1:p.Arg237HisfsTer2
ENST00000337432.9:c.710del MANE Select ENSP00000336701.4:p.Arg237HisfsTer2
NM_058216.2:c.710del NP_478123.1:p.Arg237HisfsTer2
NR_103872.1:n.614del
NR_103872.2:n.585del
ENST00000337432.8:c.710del ENSP00000336701.4:p.Arg237HisfsTer2
ENST00000413590.5:c.348del
ENST00000425173.5:c.626del ENSP00000407282.1:p.Arg209HisfsTer2
ENST00000461271.5:c.359del ENSP00000464056.1:p.Arg120HisfsTer2
ENST00000461271.6:c.359del ENSP00000464056.2:p.Arg120HisfsTer2
ENST00000475762.5:c.*1413del ENSP00000432421.1:n.*1413del
ENST00000482007.5:c.*138del ENSP00000433332.1:n.*138del
ENST00000487525.5:c.*283del ENSP00000431637.1:n.*283del
ENST00000578151.1:n.45del
ENST00000581221.5:n.225del
ENST00000583539.5:c.710del ENSP00000463121.1:p.Arg237HisfsTer2
ENST00000584617.5:c.432del
ENST00000584804.1:c.5del ENSP00000463658.1:p.Arg2HisfsTer2
ENST00000697678.1:n.612del
ENST00000697679.1:n.1784del
ENST00000697680.1:c.*1574del ENSP00000513392.1:n.*1574del
ENST00000697681.1:c.*1871del ENSP00000513393.1:n.*1871del
ENST00000697683.1:c.*1574del ENSP00000513395.1:n.*1574del
ENST00000697684.1:n.770del
ENST00000697685.1:c.*1407del ENSP00000513396.1:n.*1407del
ENST00000697686.1:c.359del ENSP00000513397.1:p.Arg120HisfsTer2
ENST00000697687.1:n.589del
ENST00000697688.1:n.756del
ENST00000697689.1:c.*1246del ENSP00000513398.1:n.*1246del
ENST00000697690.1:c.710del ENSP00000513399.1:p.Arg237HisfsTer2
ENST00000697691.1:c.*682del ENSP00000513400.1:n.*682del
ENST00000697692.1:c.*722del ENSP00000513401.1:n.*722del
ENST00000697694.1:c.359del ENSP00000513402.1:p.Arg120HisfsTer2
ENST00000697695.1:n.1317del
XM_006722001.2:c.710del XP_006722064.1:p.Arg237HisfsTer2
XM_006722001.4:c.710del XP_006722064.1:p.Arg237HisfsTer2
XM_006722002.2:c.710del XP_006722065.1:p.Arg237HisfsTer2
XM_006722002.4:c.710del XP_006722065.1:p.Arg237HisfsTer2
XM_006722004.2:c.359del XP_006722067.1:p.Arg120HisfsTer2
XM_006722004.3:c.359del XP_006722067.1:p.Arg120HisfsTer2
XM_006722005.2:c.359del XP_006722068.1:p.Arg120HisfsTer2
XM_006722005.3:c.359del XP_006722068.1:p.Arg120HisfsTer2
XM_011525092.1:c.359del XP_011523394.1:p.Arg120HisfsTer2
XM_011525092.2:c.359del XP_011523394.1:p.Arg120HisfsTer2
XM_011525093.1:c.359del XP_011523395.1:p.Arg120HisfsTer2
XM_011525093.2:c.359del XP_011523395.1:p.Arg120HisfsTer2
XM_011525094.1:c.359del XP_011523396.1:p.Arg120HisfsTer2
XM_011525094.2:c.359del XP_011523396.1:p.Arg120HisfsTer2
XM_017024914.1:c.359del XP_016880403.1:p.Arg120HisfsTer2
XM_017024915.1:c.359del XP_016880404.1:p.Arg120HisfsTer2
XM_017024916.1:c.359del XP_016880405.1:p.Arg120HisfsTer2
XM_017024917.1:c.359del XP_016880406.1:p.Arg120HisfsTer2
XM_017024918.2:c.359del XP_016880407.1:p.Arg120HisfsTer2
XM_017024919.1:c.359del XP_016880408.1:p.Arg120HisfsTer2
XR_934513.1:n.928del
XR_934513.3:n.1359del
XR_934514.1:n.928del
XR_934514.3:n.1359del