Canonical Allele Identifier: CA3261179538
Community Standard Title: NM_058216.3(RAD51C):c.640_642delinsTGC (p.Arg214Cys)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703264_58703266delinsTGC , CM000679.2:g.58703264_58703266delinsTGC GRCh38
NC_000017.10:g.56780625_56780627delinsTGC , CM000679.1:g.56780625_56780627delinsTGC GRCh37
NC_000017.9:g.54135624_54135626delinsTGC NCBI36
NG_023199.1:g.15663_15665delinsTGC , LRG_314:g.15663_15665delinsTGC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.640_642delinsTGC MANE Select NP_478123.1:p.Arg214Cys
ENST00000337432.9:c.640_642delinsTGC MANE Select ENSP00000336701.4:p.Arg214Cys
NM_058216.2:c.640_642delinsTGC NP_478123.1:p.Arg214Cys
NR_103872.1:n.544_546delinsTGC
NR_103872.2:n.515_517delinsTGC
ENST00000337432.8:c.640_642delinsTGC ENSP00000336701.4:p.Arg214Cys
ENST00000413590.5:c.278_280delinsTGC
ENST00000425173.5:c.436_438delinsTGC ENSP00000407282.1:p.Arg146Cys
ENST00000461271.5:c.289_291delinsTGC ENSP00000464056.1:p.Arg97Cys
ENST00000461271.6:c.289_291delinsTGC ENSP00000464056.2:p.Arg97Cys
ENST00000475762.5:c.*1343_*1345delinsTGC ENSP00000432421.1:n.*1343_*1345delinsTGC
ENST00000482007.5:c.*68_*70delinsTGC ENSP00000433332.1:n.*68_*70delinsTGC
ENST00000487525.5:c.*68_*70delinsTGC ENSP00000431637.1:n.*68_*70delinsTGC
ENST00000487921.5:n.552_554delinsTGC
ENST00000583539.5:c.640_642delinsTGC ENSP00000463121.1:p.Arg214Cys
ENST00000584617.5:c.362_364delinsTGC
ENST00000697677.1:n.1721_1723delinsTGC
ENST00000697678.1:n.542_544delinsTGC
ENST00000697679.1:n.1714_1716delinsTGC
ENST00000697680.1:c.*1504_*1506delinsTGC ENSP00000513392.1:n.*1504_*1506delinsTGC
ENST00000697681.1:c.*1656_*1658delinsTGC ENSP00000513393.1:n.*1656_*1658delinsTGC
ENST00000697683.1:c.*1504_*1506delinsTGC ENSP00000513395.1:n.*1504_*1506delinsTGC
ENST00000697684.1:n.700_702delinsTGC
ENST00000697685.1:c.*1337_*1339delinsTGC ENSP00000513396.1:n.*1337_*1339delinsTGC
ENST00000697686.1:c.289_291delinsTGC ENSP00000513397.1:p.Arg97Cys
ENST00000697687.1:n.519_521delinsTGC
ENST00000697688.1:n.686_688delinsTGC
ENST00000697689.1:c.*1176_*1178delinsTGC ENSP00000513398.1:n.*1176_*1178delinsTGC
ENST00000697690.1:c.640_642delinsTGC ENSP00000513399.1:p.Arg214Cys
ENST00000697691.1:c.*612_*614delinsTGC ENSP00000513400.1:n.*612_*614delinsTGC
ENST00000697692.1:c.*652_*654delinsTGC ENSP00000513401.1:n.*652_*654delinsTGC
ENST00000697694.1:c.289_291delinsTGC ENSP00000513402.1:p.Arg97Cys
ENST00000697695.1:n.1247_1249delinsTGC
XM_006722001.2:c.640_642delinsTGC XP_006722064.1:p.Arg214Cys
XM_006722001.4:c.640_642delinsTGC XP_006722064.1:p.Arg214Cys
XM_006722002.2:c.640_642delinsTGC XP_006722065.1:p.Arg214Cys
XM_006722002.4:c.640_642delinsTGC XP_006722065.1:p.Arg214Cys
XM_006722004.2:c.289_291delinsTGC XP_006722067.1:p.Arg97Cys
XM_006722004.3:c.289_291delinsTGC XP_006722067.1:p.Arg97Cys
XM_006722005.2:c.289_291delinsTGC XP_006722068.1:p.Arg97Cys
XM_006722005.3:c.289_291delinsTGC XP_006722068.1:p.Arg97Cys
XM_011525092.1:c.289_291delinsTGC XP_011523394.1:p.Arg97Cys
XM_011525092.2:c.289_291delinsTGC XP_011523394.1:p.Arg97Cys
XM_011525093.1:c.289_291delinsTGC XP_011523395.1:p.Arg97Cys
XM_011525093.2:c.289_291delinsTGC XP_011523395.1:p.Arg97Cys
XM_011525094.1:c.289_291delinsTGC XP_011523396.1:p.Arg97Cys
XM_011525094.2:c.289_291delinsTGC XP_011523396.1:p.Arg97Cys
XM_017024914.1:c.289_291delinsTGC XP_016880403.1:p.Arg97Cys
XM_017024915.1:c.289_291delinsTGC XP_016880404.1:p.Arg97Cys
XM_017024916.1:c.289_291delinsTGC XP_016880405.1:p.Arg97Cys
XM_017024917.1:c.289_291delinsTGC XP_016880406.1:p.Arg97Cys
XM_017024918.2:c.289_291delinsTGC XP_016880407.1:p.Arg97Cys
XM_017024919.1:c.289_291delinsTGC XP_016880408.1:p.Arg97Cys
XR_934513.1:n.713_715delinsTGC
XR_934513.3:n.1144_1146delinsTGC
XR_934514.1:n.713_715delinsTGC
XR_934514.3:n.1144_1146delinsTGC