Canonical Allele Identifier: CA3057243361
Community Standard Title: NM_058216.3(RAD51C):c.999_1001del (p.Glu334del)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58732517_58732519del , CM000679.2:g.58732517_58732519del GRCh38
NC_000017.10:g.56809878_56809880del , CM000679.1:g.56809878_56809880del GRCh37
NC_000017.9:g.54164877_54164879del NCBI36
NG_023199.1:g.44916_44918del , LRG_314:g.44916_44918del

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.999_1001del MANE Select NP_478123.1:p.Glu334del
ENST00000337432.9:c.999_1001del MANE Select ENSP00000336701.4:p.Glu334del
NM_058216.2:c.999_1001del NP_478123.1:p.Glu334del
NR_103872.1:n.903_905del
NR_103872.2:n.874_876del
ENST00000337432.8:c.999_1001del ENSP00000336701.4:p.Glu334del
ENST00000413590.5:c.640_642del
ENST00000461271.6:c.648_650del ENSP00000464056.2:p.Glu217del
ENST00000461706.1:n.186_188del
ENST00000475762.5:c.*1635_*1637del ENSP00000432421.1:n.*1635_*1637del
ENST00000482007.5:c.*427_*429del ENSP00000433332.1:n.*427_*429del
ENST00000487525.5:c.*575_*577del ENSP00000431637.1:n.*575_*577del
ENST00000578151.1:n.240-1601_240-1599del
ENST00000581221.5:n.514_516del
ENST00000583539.5:c.999_1001del ENSP00000463121.1:p.Glu334del
ENST00000584617.5:c.721_723del
ENST00000584804.1:c.233_235del ENSP00000463658.1:p.Arg78del
ENST00000697680.1:c.*1963_*1965del ENSP00000513392.1:n.*1963_*1965del
ENST00000697681.1:c.*2160_*2162del ENSP00000513393.1:n.*2160_*2162del
ENST00000697683.1:c.*1935_*1937del ENSP00000513395.1:n.*1935_*1937del
ENST00000697685.1:c.*1696_*1698del ENSP00000513396.1:n.*1696_*1698del
ENST00000697686.1:c.770_772del ENSP00000513397.1:p.Arg257del
ENST00000697689.1:c.*1441-1601_*1441-1599del ENSP00000513398.1:n.*1441-1601_*1441-1599del
ENST00000697690.1:c.905-1601_905-1599del ENSP00000513399.1:n.905-1601_905-1599del
ENST00000697691.1:c.*971_*973del ENSP00000513400.1:n.*971_*973del
ENST00000697692.1:c.*1011_*1013del ENSP00000513401.1:n.*1011_*1013del
ENST00000697694.1:c.648_650del ENSP00000513402.1:p.Glu217del
ENST00000697695.1:n.1606_1608del
XM_006722001.2:c.1002_1004del XP_006722064.1:p.Glu335del
XM_006722001.4:c.1002_1004del XP_006722064.1:p.Glu335del
XM_006722002.2:c.938_940del XP_006722065.1:p.Arg313del
XM_006722002.4:c.938_940del XP_006722065.1:p.Arg313del
XM_006722004.2:c.651_653del XP_006722067.1:p.Glu218del
XM_006722004.3:c.651_653del XP_006722067.1:p.Glu218del
XM_006722005.2:c.651_653del XP_006722068.1:p.Glu218del
XM_006722005.3:c.651_653del XP_006722068.1:p.Glu218del
XM_011525092.1:c.651_653del XP_011523394.1:p.Glu218del
XM_011525092.2:c.651_653del XP_011523394.1:p.Glu218del
XM_011525093.1:c.651_653del XP_011523395.1:p.Glu218del
XM_011525093.2:c.651_653del XP_011523395.1:p.Glu218del
XM_011525094.1:c.651_653del XP_011523396.1:p.Glu218del
XM_011525094.2:c.651_653del XP_011523396.1:p.Glu218del
XM_017024914.1:c.648_650del XP_016880403.1:p.Glu217del
XM_017024915.1:c.648_650del XP_016880404.1:p.Glu217del
XM_017024916.1:c.648_650del XP_016880405.1:p.Glu217del
XM_017024917.1:c.648_650del XP_016880406.1:p.Glu217del
XM_017024918.2:c.648_650del XP_016880407.1:p.Glu217del
XM_017024919.1:c.587_589del XP_016880408.1:p.Arg196del
XR_934513.1:n.1217_1219del
XR_934513.3:n.1648_1650del
XR_934514.1:n.1220_1222del
XR_934514.3:n.1651_1653del
XR_934886.1:n.149+5553_149+5555del
XR_934886.2:n.149+5553_149+5555del