Canonical Allele Identifier: CA3060598406
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703265_58703266delinsAC , CM000679.2:g.58703265_58703266delinsAC GRCh38
NC_000017.10:g.56780626_56780627delinsAC , CM000679.1:g.56780626_56780627delinsAC GRCh37
NC_000017.9:g.54135625_54135626delinsAC NCBI36
NG_023199.1:g.15664_15665delinsAC , LRG_314:g.15664_15665delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.290_291delinsAC ENSP00000464056.2:p.Arg97His
ENST00000697677.1:n.1722_1723delinsAC
ENST00000697678.1:n.543_544delinsAC
ENST00000697679.1:n.1715_1716delinsAC
ENST00000697680.1:c.*1505_*1506delinsAC ENSP00000513392.1:n.*1505_*1506delinsAC
ENST00000697681.1:c.*1657_*1658delinsAC ENSP00000513393.1:n.*1657_*1658delinsAC
ENST00000697683.1:c.*1505_*1506delinsAC ENSP00000513395.1:n.*1505_*1506delinsAC
ENST00000697684.1:n.701_702delinsAC
ENST00000697685.1:c.*1338_*1339delinsAC ENSP00000513396.1:n.*1338_*1339delinsAC
ENST00000697686.1:c.290_291delinsAC ENSP00000513397.1:p.Arg97His
ENST00000697687.1:n.520_521delinsAC
ENST00000697688.1:n.687_688delinsAC
ENST00000697689.1:c.*1177_*1178delinsAC ENSP00000513398.1:n.*1177_*1178delinsAC
ENST00000697690.1:c.641_642delinsAC ENSP00000513399.1:p.Arg214His
ENST00000697691.1:c.*613_*614delinsAC ENSP00000513400.1:n.*613_*614delinsAC
ENST00000697692.1:c.*653_*654delinsAC ENSP00000513401.1:n.*653_*654delinsAC
ENST00000697694.1:c.290_291delinsAC ENSP00000513402.1:p.Arg97His
ENST00000697695.1:n.1248_1249delinsAC
ENST00000337432.9:c.641_642delinsAC MANE Select ENSP00000336701.4:p.Arg214His
ENST00000337432.8:c.641_642delinsAC ENSP00000336701.4:p.Arg214His
ENST00000413590.5:c.279_280delinsAC
ENST00000425173.5:c.437_438delinsAC ENSP00000407282.1:p.Arg146His
ENST00000461271.5:c.290_291delinsAC ENSP00000464056.1:p.Arg97His
ENST00000475762.5:c.*1344_*1345delinsAC ENSP00000432421.1:n.*1344_*1345delinsAC
ENST00000482007.5:c.*69_*70delinsAC ENSP00000433332.1:n.*69_*70delinsAC
ENST00000487525.5:c.*69_*70delinsAC ENSP00000431637.1:n.*69_*70delinsAC
ENST00000487921.5:n.553_554delinsAC
ENST00000583539.5:c.641_642delinsAC ENSP00000463121.1:p.Arg214His
ENST00000584617.5:c.363_364delinsAC
NM_058216.2:c.641_642delinsAC NP_478123.1:p.Arg214His
NR_103872.1:n.545_546delinsAC
XM_006722001.2:c.641_642delinsAC XP_006722064.1:p.Arg214His
XM_006722002.2:c.641_642delinsAC XP_006722065.1:p.Arg214His
XM_006722004.2:c.290_291delinsAC XP_006722067.1:p.Arg97His
XM_006722005.2:c.290_291delinsAC XP_006722068.1:p.Arg97His
XM_011525092.1:c.290_291delinsAC XP_011523394.1:p.Arg97His
XM_011525093.1:c.290_291delinsAC XP_011523395.1:p.Arg97His
XM_011525094.1:c.290_291delinsAC XP_011523396.1:p.Arg97His
XR_934513.1:n.714_715delinsAC
XR_934514.1:n.714_715delinsAC
XM_006722001.4:c.641_642delinsAC XP_006722064.1:p.Arg214His
XM_006722002.4:c.641_642delinsAC XP_006722065.1:p.Arg214His
XM_006722004.3:c.290_291delinsAC XP_006722067.1:p.Arg97His
XM_006722005.3:c.290_291delinsAC XP_006722068.1:p.Arg97His
XM_011525092.2:c.290_291delinsAC XP_011523394.1:p.Arg97His
XM_011525093.2:c.290_291delinsAC XP_011523395.1:p.Arg97His
XM_011525094.2:c.290_291delinsAC XP_011523396.1:p.Arg97His
XM_017024914.1:c.290_291delinsAC XP_016880403.1:p.Arg97His
XM_017024915.1:c.290_291delinsAC XP_016880404.1:p.Arg97His
XM_017024916.1:c.290_291delinsAC XP_016880405.1:p.Arg97His
XM_017024917.1:c.290_291delinsAC XP_016880406.1:p.Arg97His
XM_017024918.2:c.290_291delinsAC XP_016880407.1:p.Arg97His
XM_017024919.1:c.290_291delinsAC XP_016880408.1:p.Arg97His
XR_934513.3:n.1145_1146delinsAC
XR_934514.3:n.1145_1146delinsAC
NM_058216.3:c.641_642delinsAC MANE Select NP_478123.1:p.Arg214His
NR_103872.2:n.516_517delinsAC