Canonical Allele Identifier: CA3057242603
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703325del , CM000679.2:g.58703325del GRCh38
NC_000017.10:g.56780686del , CM000679.1:g.56780686del GRCh37
NC_000017.9:g.54135685del NCBI36
NG_023199.1:g.15724del , LRG_314:g.15724del

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.350del ENSP00000464056.2:p.Ser117Ter
ENST00000697677.1:n.1782del
ENST00000697678.1:n.603del
ENST00000697679.1:n.1775del
ENST00000697680.1:c.*1565del ENSP00000513392.1:n.*1565del
ENST00000697681.1:c.*1717del ENSP00000513393.1:n.*1717del
ENST00000697683.1:c.*1565del ENSP00000513395.1:n.*1565del
ENST00000697684.1:n.761del
ENST00000697685.1:c.*1398del ENSP00000513396.1:n.*1398del
ENST00000697686.1:c.350del ENSP00000513397.1:p.Ser117Ter
ENST00000697687.1:n.580del
ENST00000697688.1:n.747del
ENST00000697689.1:c.*1237del ENSP00000513398.1:n.*1237del
ENST00000697690.1:c.701del ENSP00000513399.1:p.Ser234Ter
ENST00000697691.1:c.*673del ENSP00000513400.1:n.*673del
ENST00000697692.1:c.*713del ENSP00000513401.1:n.*713del
ENST00000697694.1:c.350del ENSP00000513402.1:p.Ser117Ter
ENST00000697695.1:n.1308del
ENST00000337432.9:c.701del MANE Select ENSP00000336701.4:p.Ser234Ter
ENST00000337432.8:c.701del ENSP00000336701.4:p.Ser234Ter
ENST00000413590.5:c.339del
ENST00000425173.5:c.497del ENSP00000407282.1:p.Ser166Ter
ENST00000461271.5:c.350del ENSP00000464056.1:p.Ser117Ter
ENST00000475762.5:c.*1404del ENSP00000432421.1:n.*1404del
ENST00000482007.5:c.*129del ENSP00000433332.1:n.*129del
ENST00000487525.5:c.*129del ENSP00000431637.1:n.*129del
ENST00000487921.5:n.613del
ENST00000583539.5:c.701del ENSP00000463121.1:p.Ser234Ter
ENST00000584617.5:c.423del
NM_058216.2:c.701del NP_478123.1:p.Ser234Ter
NR_103872.1:n.605del
XM_006722001.2:c.701del XP_006722064.1:p.Ser234Ter
XM_006722002.2:c.701del XP_006722065.1:p.Ser234Ter
XM_006722004.2:c.350del XP_006722067.1:p.Ser117Ter
XM_006722005.2:c.350del XP_006722068.1:p.Ser117Ter
XM_011525092.1:c.350del XP_011523394.1:p.Ser117Ter
XM_011525093.1:c.350del XP_011523395.1:p.Ser117Ter
XM_011525094.1:c.350del XP_011523396.1:p.Ser117Ter
XR_934513.1:n.774del
XR_934514.1:n.774del
XM_006722001.4:c.701del XP_006722064.1:p.Ser234Ter
XM_006722002.4:c.701del XP_006722065.1:p.Ser234Ter
XM_006722004.3:c.350del XP_006722067.1:p.Ser117Ter
XM_006722005.3:c.350del XP_006722068.1:p.Ser117Ter
XM_011525092.2:c.350del XP_011523394.1:p.Ser117Ter
XM_011525093.2:c.350del XP_011523395.1:p.Ser117Ter
XM_011525094.2:c.350del XP_011523396.1:p.Ser117Ter
XM_017024914.1:c.350del XP_016880403.1:p.Ser117Ter
XM_017024915.1:c.350del XP_016880404.1:p.Ser117Ter
XM_017024916.1:c.350del XP_016880405.1:p.Ser117Ter
XM_017024917.1:c.350del XP_016880406.1:p.Ser117Ter
XM_017024918.2:c.350del XP_016880407.1:p.Ser117Ter
XM_017024919.1:c.350del XP_016880408.1:p.Ser117Ter
XR_934513.3:n.1205del
XR_934514.3:n.1205del
NM_058216.3:c.701del MANE Select NP_478123.1:p.Ser234Ter
NR_103872.2:n.576del