Canonical Allele Identifier: CA3057243377
Community Standard Title: NM_058216.3(RAD51C):c.1057_1059del (p.Ser353del)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734148_58734150del , CM000679.2:g.58734148_58734150del GRCh38
NC_000017.10:g.56811509_56811511del , CM000679.1:g.56811509_56811511del GRCh37
NC_000017.9:g.54166508_54166510del NCBI36
NG_023199.1:g.46547_46549del , LRG_314:g.46547_46549del

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1057_1059del MANE Select NP_478123.1:p.Ser353del
ENST00000337432.9:c.1057_1059del MANE Select ENSP00000336701.4:p.Ser353del
NM_058216.2:c.1057_1059del NP_478123.1:p.Ser353del
NR_103872.1:n.961_963del
NR_103872.2:n.932_934del
ENST00000337432.8:c.1057_1059del ENSP00000336701.4:p.Ser353del
ENST00000413590.5:c.698_700del
ENST00000461271.6:c.*1589_*1591del ENSP00000464056.2:n.*1589_*1591del
ENST00000461706.1:n.244_246del
ENST00000475762.5:c.*1693_*1695del ENSP00000432421.1:n.*1693_*1695del
ENST00000482007.5:c.*485_*487del ENSP00000433332.1:n.*485_*487del
ENST00000487525.5:c.*633_*635del ENSP00000431637.1:n.*633_*635del
ENST00000578151.1:n.270_272del
ENST00000581221.5:n.572_574del
ENST00000584804.1:c.291_293del ENSP00000463658.1:p.Leu98del
ENST00000697680.1:c.*2021_*2023del ENSP00000513392.1:n.*2021_*2023del
ENST00000697681.1:c.*2218_*2220del ENSP00000513393.1:n.*2218_*2220del
ENST00000697683.1:c.*1993_*1995del ENSP00000513395.1:n.*1993_*1995del
ENST00000697685.1:c.*1754_*1756del ENSP00000513396.1:n.*1754_*1756del
ENST00000697686.1:c.828_830del ENSP00000513397.1:p.Leu277del
ENST00000697689.1:c.*1471_*1473del ENSP00000513398.1:n.*1471_*1473del
ENST00000697690.1:c.*17_*19del ENSP00000513399.1:n.*17_*19del
ENST00000697691.1:c.*1029_*1031del ENSP00000513400.1:n.*1029_*1031del
ENST00000697692.1:c.*1069_*1071del ENSP00000513401.1:n.*1069_*1071del
ENST00000697694.1:c.706_708del ENSP00000513402.1:p.Ser236del
ENST00000697695.1:n.1664_1666del
XM_006722001.2:c.1060_1062del XP_006722064.1:p.Ser354del
XM_006722001.4:c.1060_1062del XP_006722064.1:p.Ser354del
XM_006722002.2:c.996_998del XP_006722065.1:p.Leu333del
XM_006722002.4:c.996_998del XP_006722065.1:p.Leu333del
XM_006722004.2:c.709_711del XP_006722067.1:p.Ser237del
XM_006722004.3:c.709_711del XP_006722067.1:p.Ser237del
XM_006722005.2:c.709_711del XP_006722068.1:p.Ser237del
XM_006722005.3:c.709_711del XP_006722068.1:p.Ser237del
XM_011525092.1:c.709_711del XP_011523394.1:p.Ser237del
XM_011525092.2:c.709_711del XP_011523394.1:p.Ser237del
XM_011525093.1:c.709_711del XP_011523395.1:p.Ser237del
XM_011525093.2:c.709_711del XP_011523395.1:p.Ser237del
XM_011525094.1:c.709_711del XP_011523396.1:p.Ser237del
XM_011525094.2:c.709_711del XP_011523396.1:p.Ser237del
XM_017024914.1:c.706_708del XP_016880403.1:p.Ser236del
XM_017024915.1:c.706_708del XP_016880404.1:p.Ser236del
XM_017024916.1:c.706_708del XP_016880405.1:p.Ser236del
XM_017024917.1:c.706_708del XP_016880406.1:p.Ser236del
XM_017024918.2:c.706_708del XP_016880407.1:p.Ser236del
XM_017024919.1:c.645_647del XP_016880408.1:p.Leu216del
XR_934513.1:n.1275_1277del
XR_934513.3:n.1706_1708del
XR_934514.1:n.1278_1280del
XR_934514.3:n.1709_1711del
XR_934886.1:n.149+3923_149+3925del
XR_934886.2:n.149+3923_149+3925del