Canonical Allele Identifier: CA3261178683
Community Standard Title: NM_058216.3(RAD51C):c.856_858delinsGTC (p.Met286Val)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58720764_58720766delinsGTC , CM000679.2:g.58720764_58720766delinsGTC GRCh38
NC_000017.10:g.56798125_56798127delinsGTC , CM000679.1:g.56798125_56798127delinsGTC GRCh37
NC_000017.9:g.54153124_54153126delinsGTC NCBI36
NG_023199.1:g.33163_33165delinsGTC , LRG_314:g.33163_33165delinsGTC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.856_858delinsGTC MANE Select NP_478123.1:p.Met286Val
ENST00000337432.9:c.856_858delinsGTC MANE Select ENSP00000336701.4:p.Met286Val
NM_058216.2:c.856_858delinsGTC NP_478123.1:p.Met286Val
NR_103872.1:n.760_762delinsGTC
NR_103872.2:n.731_733delinsGTC
ENST00000337432.8:c.856_858delinsGTC ENSP00000336701.4:p.Met286Val
ENST00000413590.5:c.494_496delinsGTC
ENST00000461271.6:c.505_507delinsGTC ENSP00000464056.2:p.Met169Val
ENST00000475762.5:c.*1541-3276_*1541-3274delinsGTC ENSP00000432421.1:n.*1541-3276_*1541-3274delinsGTC
ENST00000482007.5:c.*284_*286delinsGTC ENSP00000433332.1:n.*284_*286delinsGTC
ENST00000487525.5:c.*429_*431delinsGTC ENSP00000431637.1:n.*429_*431delinsGTC
ENST00000578151.1:n.191_193delinsGTC
ENST00000581221.5:n.371_373delinsGTC
ENST00000583539.5:c.856_858delinsGTC ENSP00000463121.1:p.Met286Val
ENST00000584617.5:c.578_580delinsGTC
ENST00000584804.1:c.151_153delinsGTC ENSP00000463658.1:p.Met51Val
ENST00000697678.1:n.758_760delinsGTC
ENST00000697679.1:n.1930_1932delinsGTC
ENST00000697680.1:c.*1820_*1822delinsGTC ENSP00000513392.1:n.*1820_*1822delinsGTC
ENST00000697681.1:c.*2017_*2019delinsGTC ENSP00000513393.1:n.*2017_*2019delinsGTC
ENST00000697683.1:c.*1720_*1722delinsGTC ENSP00000513395.1:n.*1720_*1722delinsGTC
ENST00000697684.1:n.916_918delinsGTC
ENST00000697685.1:c.*1553_*1555delinsGTC ENSP00000513396.1:n.*1553_*1555delinsGTC
ENST00000697686.1:c.505_507delinsGTC ENSP00000513397.1:p.Met169Val
ENST00000697687.1:n.735_737delinsGTC
ENST00000697688.1:n.902_904delinsGTC
ENST00000697689.1:c.*1392_*1394delinsGTC ENSP00000513398.1:n.*1392_*1394delinsGTC
ENST00000697690.1:c.856_858delinsGTC ENSP00000513399.1:p.Met286Val
ENST00000697691.1:c.*828_*830delinsGTC ENSP00000513400.1:n.*828_*830delinsGTC
ENST00000697692.1:c.*868_*870delinsGTC ENSP00000513401.1:n.*868_*870delinsGTC
ENST00000697694.1:c.505_507delinsGTC ENSP00000513402.1:p.Met169Val
ENST00000697695.1:n.1463_1465delinsGTC
XM_006722001.2:c.856_858delinsGTC XP_006722064.1:p.Met286Val
XM_006722001.4:c.856_858delinsGTC XP_006722064.1:p.Met286Val
XM_006722002.2:c.856_858delinsGTC XP_006722065.1:p.Met286Val
XM_006722002.4:c.856_858delinsGTC XP_006722065.1:p.Met286Val
XM_006722004.2:c.505_507delinsGTC XP_006722067.1:p.Met169Val
XM_006722004.3:c.505_507delinsGTC XP_006722067.1:p.Met169Val
XM_006722005.2:c.505_507delinsGTC XP_006722068.1:p.Met169Val
XM_006722005.3:c.505_507delinsGTC XP_006722068.1:p.Met169Val
XM_011525092.1:c.505_507delinsGTC XP_011523394.1:p.Met169Val
XM_011525092.2:c.505_507delinsGTC XP_011523394.1:p.Met169Val
XM_011525093.1:c.505_507delinsGTC XP_011523395.1:p.Met169Val
XM_011525093.2:c.505_507delinsGTC XP_011523395.1:p.Met169Val
XM_011525094.1:c.505_507delinsGTC XP_011523396.1:p.Met169Val
XM_011525094.2:c.505_507delinsGTC XP_011523396.1:p.Met169Val
XM_017024914.1:c.505_507delinsGTC XP_016880403.1:p.Met169Val
XM_017024915.1:c.505_507delinsGTC XP_016880404.1:p.Met169Val
XM_017024916.1:c.505_507delinsGTC XP_016880405.1:p.Met169Val
XM_017024917.1:c.505_507delinsGTC XP_016880406.1:p.Met169Val
XM_017024918.2:c.505_507delinsGTC XP_016880407.1:p.Met169Val
XM_017024919.1:c.505_507delinsGTC XP_016880408.1:p.Met169Val
XR_934513.1:n.1074_1076delinsGTC
XR_934513.3:n.1505_1507delinsGTC
XR_934514.1:n.1074_1076delinsGTC
XR_934514.3:n.1505_1507delinsGTC