Canonical Allele Identifier: CA2580094398
Community Standard Title: NM_058216.3(RAD51C):c.1000_1002del (p.Glu334del)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58732518_58732520del , CM000679.2:g.58732518_58732520del GRCh38
NC_000017.10:g.56809879_56809881del , CM000679.1:g.56809879_56809881del GRCh37
NC_000017.9:g.54164878_54164880del NCBI36
NG_023199.1:g.44917_44919del , LRG_314:g.44917_44919del

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1000_1002del MANE Select NP_478123.1:p.Glu334del
ENST00000337432.9:c.1000_1002del MANE Select ENSP00000336701.4:p.Glu334del
NM_058216.2:c.1000_1002del NP_478123.1:p.Glu334del
NR_103872.1:n.904_906del
NR_103872.2:n.875_877del
ENST00000337432.8:c.1000_1002del ENSP00000336701.4:p.Glu334del
ENST00000413590.5:c.641_643del
ENST00000461271.6:c.649_651del ENSP00000464056.2:p.Glu217del
ENST00000461706.1:n.187_189del
ENST00000475762.5:c.*1636_*1638del ENSP00000432421.1:n.*1636_*1638del
ENST00000482007.5:c.*428_*430del ENSP00000433332.1:n.*428_*430del
ENST00000487525.5:c.*576_*578del ENSP00000431637.1:n.*576_*578del
ENST00000578151.1:n.240-1600_240-1598del
ENST00000581221.5:n.515_517del
ENST00000583539.5:c.1000_1002del ENSP00000463121.1:p.Glu334del
ENST00000584804.1:c.234_236del ENSP00000463658.1:p.Arg78_Asn79delinsSer
ENST00000697680.1:c.*1964_*1966del ENSP00000513392.1:n.*1964_*1966del
ENST00000697681.1:c.*2161_*2163del ENSP00000513393.1:n.*2161_*2163del
ENST00000697683.1:c.*1936_*1938del ENSP00000513395.1:n.*1936_*1938del
ENST00000697685.1:c.*1697_*1699del ENSP00000513396.1:n.*1697_*1699del
ENST00000697686.1:c.771_773del ENSP00000513397.1:p.Arg257_Asn258delinsSer
ENST00000697689.1:c.*1441-1600_*1441-1598del ENSP00000513398.1:n.*1441-1600_*1441-1598del
ENST00000697690.1:c.905-1600_905-1598del ENSP00000513399.1:n.905-1600_905-1598del
ENST00000697691.1:c.*972_*974del ENSP00000513400.1:n.*972_*974del
ENST00000697692.1:c.*1012_*1014del ENSP00000513401.1:n.*1012_*1014del
ENST00000697694.1:c.649_651del ENSP00000513402.1:p.Glu217del
ENST00000697695.1:n.1607_1609del
XM_006722001.2:c.1003_1005del XP_006722064.1:p.Glu335del
XM_006722001.4:c.1003_1005del XP_006722064.1:p.Glu335del
XM_006722002.2:c.939_941del XP_006722065.1:p.Arg313_Asn314delinsSer
XM_006722002.4:c.939_941del XP_006722065.1:p.Arg313_Asn314delinsSer
XM_006722004.2:c.652_654del XP_006722067.1:p.Glu218del
XM_006722004.3:c.652_654del XP_006722067.1:p.Glu218del
XM_006722005.2:c.652_654del XP_006722068.1:p.Glu218del
XM_006722005.3:c.652_654del XP_006722068.1:p.Glu218del
XM_011525092.1:c.652_654del XP_011523394.1:p.Glu218del
XM_011525092.2:c.652_654del XP_011523394.1:p.Glu218del
XM_011525093.1:c.652_654del XP_011523395.1:p.Glu218del
XM_011525093.2:c.652_654del XP_011523395.1:p.Glu218del
XM_011525094.1:c.652_654del XP_011523396.1:p.Glu218del
XM_011525094.2:c.652_654del XP_011523396.1:p.Glu218del
XM_017024914.1:c.649_651del XP_016880403.1:p.Glu217del
XM_017024915.1:c.649_651del XP_016880404.1:p.Glu217del
XM_017024916.1:c.649_651del XP_016880405.1:p.Glu217del
XM_017024917.1:c.649_651del XP_016880406.1:p.Glu217del
XM_017024918.2:c.649_651del XP_016880407.1:p.Glu217del
XM_017024919.1:c.588_590del XP_016880408.1:p.Arg196_Asn197delinsSer
XR_934513.1:n.1218_1220del
XR_934513.3:n.1649_1651del
XR_934514.1:n.1221_1223del
XR_934514.3:n.1652_1654del
XR_934886.1:n.149+5551_149+5553del
XR_934886.2:n.149+5551_149+5553del