Canonical Allele Identifier: CA3261180310
Community Standard Title: NM_058216.3(RAD51C):c.688_690delinsTTC (p.Leu230Phe)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703312_58703314delinsTTC , CM000679.2:g.58703312_58703314delinsTTC GRCh38
NC_000017.10:g.56780673_56780675delinsTTC , CM000679.1:g.56780673_56780675delinsTTC GRCh37
NC_000017.9:g.54135672_54135674delinsTTC NCBI36
NG_023199.1:g.15711_15713delinsTTC , LRG_314:g.15711_15713delinsTTC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.688_690delinsTTC MANE Select NP_478123.1:p.Leu230Phe
ENST00000337432.9:c.688_690delinsTTC MANE Select ENSP00000336701.4:p.Leu230Phe
NM_058216.2:c.688_690delinsTTC NP_478123.1:p.Leu230Phe
NR_103872.1:n.592_594delinsTTC
NR_103872.2:n.563_565delinsTTC
ENST00000337432.8:c.688_690delinsTTC ENSP00000336701.4:p.Leu230Phe
ENST00000413590.5:c.326_328delinsTTC
ENST00000425173.5:c.484_486delinsTTC ENSP00000407282.1:p.Leu162Phe
ENST00000461271.5:c.337_339delinsTTC ENSP00000464056.1:p.Leu113Phe
ENST00000461271.6:c.337_339delinsTTC ENSP00000464056.2:p.Leu113Phe
ENST00000475762.5:c.*1391_*1393delinsTTC ENSP00000432421.1:n.*1391_*1393delinsTTC
ENST00000482007.5:c.*116_*118delinsTTC ENSP00000433332.1:n.*116_*118delinsTTC
ENST00000487525.5:c.*116_*118delinsTTC ENSP00000431637.1:n.*116_*118delinsTTC
ENST00000487921.5:n.600_602delinsTTC
ENST00000583539.5:c.688_690delinsTTC ENSP00000463121.1:p.Leu230Phe
ENST00000584617.5:c.410_412delinsTTC
ENST00000697677.1:n.1769_1771delinsTTC
ENST00000697678.1:n.590_592delinsTTC
ENST00000697679.1:n.1762_1764delinsTTC
ENST00000697680.1:c.*1552_*1554delinsTTC ENSP00000513392.1:n.*1552_*1554delinsTTC
ENST00000697681.1:c.*1704_*1706delinsTTC ENSP00000513393.1:n.*1704_*1706delinsTTC
ENST00000697683.1:c.*1552_*1554delinsTTC ENSP00000513395.1:n.*1552_*1554delinsTTC
ENST00000697684.1:n.748_750delinsTTC
ENST00000697685.1:c.*1385_*1387delinsTTC ENSP00000513396.1:n.*1385_*1387delinsTTC
ENST00000697686.1:c.337_339delinsTTC ENSP00000513397.1:p.Leu113Phe
ENST00000697687.1:n.567_569delinsTTC
ENST00000697688.1:n.734_736delinsTTC
ENST00000697689.1:c.*1224_*1226delinsTTC ENSP00000513398.1:n.*1224_*1226delinsTTC
ENST00000697690.1:c.688_690delinsTTC ENSP00000513399.1:p.Leu230Phe
ENST00000697691.1:c.*660_*662delinsTTC ENSP00000513400.1:n.*660_*662delinsTTC
ENST00000697692.1:c.*700_*702delinsTTC ENSP00000513401.1:n.*700_*702delinsTTC
ENST00000697694.1:c.337_339delinsTTC ENSP00000513402.1:p.Leu113Phe
ENST00000697695.1:n.1295_1297delinsTTC
XM_006722001.2:c.688_690delinsTTC XP_006722064.1:p.Leu230Phe
XM_006722001.4:c.688_690delinsTTC XP_006722064.1:p.Leu230Phe
XM_006722002.2:c.688_690delinsTTC XP_006722065.1:p.Leu230Phe
XM_006722002.4:c.688_690delinsTTC XP_006722065.1:p.Leu230Phe
XM_006722004.2:c.337_339delinsTTC XP_006722067.1:p.Leu113Phe
XM_006722004.3:c.337_339delinsTTC XP_006722067.1:p.Leu113Phe
XM_006722005.2:c.337_339delinsTTC XP_006722068.1:p.Leu113Phe
XM_006722005.3:c.337_339delinsTTC XP_006722068.1:p.Leu113Phe
XM_011525092.1:c.337_339delinsTTC XP_011523394.1:p.Leu113Phe
XM_011525092.2:c.337_339delinsTTC XP_011523394.1:p.Leu113Phe
XM_011525093.1:c.337_339delinsTTC XP_011523395.1:p.Leu113Phe
XM_011525093.2:c.337_339delinsTTC XP_011523395.1:p.Leu113Phe
XM_011525094.1:c.337_339delinsTTC XP_011523396.1:p.Leu113Phe
XM_011525094.2:c.337_339delinsTTC XP_011523396.1:p.Leu113Phe
XM_017024914.1:c.337_339delinsTTC XP_016880403.1:p.Leu113Phe
XM_017024915.1:c.337_339delinsTTC XP_016880404.1:p.Leu113Phe
XM_017024916.1:c.337_339delinsTTC XP_016880405.1:p.Leu113Phe
XM_017024917.1:c.337_339delinsTTC XP_016880406.1:p.Leu113Phe
XM_017024918.2:c.337_339delinsTTC XP_016880407.1:p.Leu113Phe
XM_017024919.1:c.337_339delinsTTC XP_016880408.1:p.Leu113Phe
XR_934513.1:n.761_763delinsTTC
XR_934513.3:n.1192_1194delinsTTC
XR_934514.1:n.761_763delinsTTC
XR_934514.3:n.1192_1194delinsTTC