Canonical Allele Identifier: CA3057243360
Community Standard Title: NM_058216.3(RAD51C):c.997_999del (p.Lys333del)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58732515_58732517del , CM000679.2:g.58732515_58732517del GRCh38
NC_000017.10:g.56809876_56809878del , CM000679.1:g.56809876_56809878del GRCh37
NC_000017.9:g.54164875_54164877del NCBI36
NG_023199.1:g.44914_44916del , LRG_314:g.44914_44916del

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.997_999del MANE Select NP_478123.1:p.Lys333del
ENST00000337432.9:c.997_999del MANE Select ENSP00000336701.4:p.Lys333del
NM_058216.2:c.997_999del NP_478123.1:p.Lys333del
NR_103872.1:n.901_903del
NR_103872.2:n.872_874del
ENST00000337432.8:c.997_999del ENSP00000336701.4:p.Lys333del
ENST00000413590.5:c.638_640del
ENST00000461271.6:c.646_648del ENSP00000464056.2:p.Lys216del
ENST00000461706.1:n.184_186del
ENST00000475762.5:c.*1633_*1635del ENSP00000432421.1:n.*1633_*1635del
ENST00000482007.5:c.*425_*427del ENSP00000433332.1:n.*425_*427del
ENST00000487525.5:c.*573_*575del ENSP00000431637.1:n.*573_*575del
ENST00000578151.1:n.240-1603_240-1601del
ENST00000581221.5:n.512_514del
ENST00000583539.5:c.997_999del ENSP00000463121.1:p.Lys333del
ENST00000584617.5:c.719_721del
ENST00000584804.1:c.231_233del ENSP00000463658.1:p.Arg78del
ENST00000697680.1:c.*1961_*1963del ENSP00000513392.1:n.*1961_*1963del
ENST00000697681.1:c.*2158_*2160del ENSP00000513393.1:n.*2158_*2160del
ENST00000697683.1:c.*1933_*1935del ENSP00000513395.1:n.*1933_*1935del
ENST00000697685.1:c.*1694_*1696del ENSP00000513396.1:n.*1694_*1696del
ENST00000697686.1:c.768_770del ENSP00000513397.1:p.Arg257del
ENST00000697689.1:c.*1441-1603_*1441-1601del ENSP00000513398.1:n.*1441-1603_*1441-1601del
ENST00000697690.1:c.905-1603_905-1601del ENSP00000513399.1:n.905-1603_905-1601del
ENST00000697691.1:c.*969_*971del ENSP00000513400.1:n.*969_*971del
ENST00000697692.1:c.*1009_*1011del ENSP00000513401.1:n.*1009_*1011del
ENST00000697694.1:c.646_648del ENSP00000513402.1:p.Lys216del
ENST00000697695.1:n.1604_1606del
XM_006722001.2:c.1000_1002del XP_006722064.1:p.Lys334del
XM_006722001.4:c.1000_1002del XP_006722064.1:p.Lys334del
XM_006722002.2:c.936_938del XP_006722065.1:p.Arg313del
XM_006722002.4:c.936_938del XP_006722065.1:p.Arg313del
XM_006722004.2:c.649_651del XP_006722067.1:p.Lys217del
XM_006722004.3:c.649_651del XP_006722067.1:p.Lys217del
XM_006722005.2:c.649_651del XP_006722068.1:p.Lys217del
XM_006722005.3:c.649_651del XP_006722068.1:p.Lys217del
XM_011525092.1:c.649_651del XP_011523394.1:p.Lys217del
XM_011525092.2:c.649_651del XP_011523394.1:p.Lys217del
XM_011525093.1:c.649_651del XP_011523395.1:p.Lys217del
XM_011525093.2:c.649_651del XP_011523395.1:p.Lys217del
XM_011525094.1:c.649_651del XP_011523396.1:p.Lys217del
XM_011525094.2:c.649_651del XP_011523396.1:p.Lys217del
XM_017024914.1:c.646_648del XP_016880403.1:p.Lys216del
XM_017024915.1:c.646_648del XP_016880404.1:p.Lys216del
XM_017024916.1:c.646_648del XP_016880405.1:p.Lys216del
XM_017024917.1:c.646_648del XP_016880406.1:p.Lys216del
XM_017024918.2:c.646_648del XP_016880407.1:p.Lys216del
XM_017024919.1:c.585_587del XP_016880408.1:p.Arg196del
XR_934513.1:n.1215_1217del
XR_934513.3:n.1646_1648del
XR_934514.1:n.1218_1220del
XR_934514.3:n.1649_1651del
XR_934886.1:n.149+5556_149+5558del
XR_934886.2:n.149+5556_149+5558del