Canonical Allele Identifier: CA3261179085
Community Standard Title: NM_058216.3(RAD51C):c.1003_1005del (p.Cys335del)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58732521_58732523del , CM000679.2:g.58732521_58732523del GRCh38
NC_000017.10:g.56809882_56809884del , CM000679.1:g.56809882_56809884del GRCh37
NC_000017.9:g.54164881_54164883del NCBI36
NG_023199.1:g.44920_44922del , LRG_314:g.44920_44922del

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1003_1005del MANE Select NP_478123.1:p.Cys335del
ENST00000337432.9:c.1003_1005del MANE Select ENSP00000336701.4:p.Cys335del
NM_058216.2:c.1003_1005del NP_478123.1:p.Cys335del
NR_103872.1:n.907_909del
NR_103872.2:n.878_880del
ENST00000337432.8:c.1003_1005del ENSP00000336701.4:p.Cys335del
ENST00000413590.5:c.644_646del
ENST00000461271.6:c.652_654del ENSP00000464056.2:p.Cys218del
ENST00000461706.1:n.190_192del
ENST00000475762.5:c.*1639_*1641del ENSP00000432421.1:n.*1639_*1641del
ENST00000482007.5:c.*431_*433del ENSP00000433332.1:n.*431_*433del
ENST00000487525.5:c.*579_*581del ENSP00000431637.1:n.*579_*581del
ENST00000578151.1:n.240-1597_240-1595del
ENST00000581221.5:n.518_520del
ENST00000583539.5:c.1003_1005del ENSP00000463121.1:p.Cys335del
ENST00000584804.1:c.237_239del ENSP00000463658.1:p.Asn79_Ala80delinsLys
ENST00000697680.1:c.*1967_*1969del ENSP00000513392.1:n.*1967_*1969del
ENST00000697681.1:c.*2164_*2166del ENSP00000513393.1:n.*2164_*2166del
ENST00000697683.1:c.*1939_*1941del ENSP00000513395.1:n.*1939_*1941del
ENST00000697685.1:c.*1700_*1702del ENSP00000513396.1:n.*1700_*1702del
ENST00000697686.1:c.774_776del ENSP00000513397.1:p.Asn258_Ala259delinsLys
ENST00000697689.1:c.*1441-1597_*1441-1595del ENSP00000513398.1:n.*1441-1597_*1441-1595del
ENST00000697690.1:c.905-1597_905-1595del ENSP00000513399.1:n.905-1597_905-1595del
ENST00000697691.1:c.*975_*977del ENSP00000513400.1:n.*975_*977del
ENST00000697692.1:c.*1015_*1017del ENSP00000513401.1:n.*1015_*1017del
ENST00000697694.1:c.652_654del ENSP00000513402.1:p.Cys218del
ENST00000697695.1:n.1610_1612del
XM_006722001.2:c.1006_1008del XP_006722064.1:p.Cys336del
XM_006722001.4:c.1006_1008del XP_006722064.1:p.Cys336del
XM_006722002.2:c.942_944del XP_006722065.1:p.Asn314_Ala315delinsLys
XM_006722002.4:c.942_944del XP_006722065.1:p.Asn314_Ala315delinsLys
XM_006722004.2:c.655_657del XP_006722067.1:p.Cys219del
XM_006722004.3:c.655_657del XP_006722067.1:p.Cys219del
XM_006722005.2:c.655_657del XP_006722068.1:p.Cys219del
XM_006722005.3:c.655_657del XP_006722068.1:p.Cys219del
XM_011525092.1:c.655_657del XP_011523394.1:p.Cys219del
XM_011525092.2:c.655_657del XP_011523394.1:p.Cys219del
XM_011525093.1:c.655_657del XP_011523395.1:p.Cys219del
XM_011525093.2:c.655_657del XP_011523395.1:p.Cys219del
XM_011525094.1:c.655_657del XP_011523396.1:p.Cys219del
XM_011525094.2:c.655_657del XP_011523396.1:p.Cys219del
XM_017024914.1:c.652_654del XP_016880403.1:p.Cys218del
XM_017024915.1:c.652_654del XP_016880404.1:p.Cys218del
XM_017024916.1:c.652_654del XP_016880405.1:p.Cys218del
XM_017024917.1:c.652_654del XP_016880406.1:p.Cys218del
XM_017024918.2:c.652_654del XP_016880407.1:p.Cys218del
XM_017024919.1:c.591_593del XP_016880408.1:p.Asn197_Ala198delinsLys
XR_934513.1:n.1221_1223del
XR_934513.3:n.1652_1654del
XR_934514.1:n.1224_1226del
XR_934514.3:n.1655_1657del
XR_934886.1:n.149+5548_149+5550del
XR_934886.2:n.149+5548_149+5550del