Canonical Allele Identifier: CA3261180980
Community Standard Title: NM_058216.3(RAD51C):c.476_477delinsTG (p.Asp159Val)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58696764_58696765delinsTG , CM000679.2:g.58696764_58696765delinsTG GRCh38
NC_000017.10:g.56774125_56774126delinsTG , CM000679.1:g.56774125_56774126delinsTG GRCh37
NC_000017.9:g.54129124_54129125delinsTG NCBI36
NG_023199.1:g.9163_9164delinsTG , LRG_314:g.9163_9164delinsTG
NG_047169.1:g.315_316delinsCA

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.476_477delinsTG MANE Select NP_478123.1:p.Asp159Val
ENST00000337432.9:c.476_477delinsTG MANE Select ENSP00000336701.4:p.Asp159Val
NM_058216.2:c.476_477delinsTG NP_478123.1:p.Asp159Val
NR_103872.1:n.475+1575_475+1576delinsTG
NR_103872.2:n.446+1575_446+1576delinsTG
ENST00000337432.8:c.476_477delinsTG ENSP00000336701.4:p.Asp159Val
ENST00000413590.5:c.114_115delinsTG
ENST00000425173.5:c.272_273delinsTG ENSP00000407282.1:p.Asp91Val
ENST00000461271.5:c.125_126delinsTG ENSP00000464056.1:p.Asp42Val
ENST00000461271.6:c.125_126delinsTG ENSP00000464056.2:p.Asp42Val
ENST00000475762.5:c.*1179_*1180delinsTG ENSP00000432421.1:n.*1179_*1180delinsTG
ENST00000482007.5:c.404+1575_404+1576delinsTG ENSP00000433332.1:n.404+1575_404+1576delinsTG
ENST00000487525.5:c.404+1575_404+1576delinsTG ENSP00000431637.1:n.404+1575_404+1576delinsTG
ENST00000487921.5:n.388_389delinsTG
ENST00000583539.5:c.476_477delinsTG ENSP00000463121.1:p.Asp159Val
ENST00000584617.5:c.198_199delinsTG
ENST00000622327.4:c.212_213delinsTG ENSP00000482326.1:p.Asp71Val
ENST00000697675.1:n.3073_3074delinsTG
ENST00000697676.1:n.536_537delinsTG
ENST00000697677.1:n.1557_1558delinsTG
ENST00000697678.1:n.378_379delinsTG
ENST00000697679.1:n.1550_1551delinsTG
ENST00000697680.1:c.*1340_*1341delinsTG ENSP00000513392.1:n.*1340_*1341delinsTG
ENST00000697681.1:c.*1367_*1368delinsTG ENSP00000513393.1:n.*1367_*1368delinsTG
ENST00000697683.1:c.*1340_*1341delinsTG ENSP00000513395.1:n.*1340_*1341delinsTG
ENST00000697684.1:n.536_537delinsTG
ENST00000697685.1:c.*1268+1575_*1268+1576delinsTG ENSP00000513396.1:n.*1268+1575_*1268+1576delinsTG
ENST00000697686.1:c.125_126delinsTG ENSP00000513397.1:p.Asp42Val
ENST00000697687.1:n.450+1575_450+1576delinsTG
ENST00000697688.1:n.522_523delinsTG
ENST00000697689.1:c.*1107+1575_*1107+1576delinsTG ENSP00000513398.1:n.*1107+1575_*1107+1576delinsTG
ENST00000697690.1:c.476_477delinsTG ENSP00000513399.1:p.Asp159Val
ENST00000697691.1:c.*448_*449delinsTG ENSP00000513400.1:n.*448_*449delinsTG
ENST00000697692.1:c.*488_*489delinsTG ENSP00000513401.1:n.*488_*489delinsTG
ENST00000697694.1:c.125_126delinsTG ENSP00000513402.1:p.Asp42Val
ENST00000697695.1:n.1083_1084delinsTG
XM_006722001.2:c.476_477delinsTG XP_006722064.1:p.Asp159Val
XM_006722001.4:c.476_477delinsTG XP_006722064.1:p.Asp159Val
XM_006722002.2:c.476_477delinsTG XP_006722065.1:p.Asp159Val
XM_006722002.4:c.476_477delinsTG XP_006722065.1:p.Asp159Val
XM_006722004.2:c.125_126delinsTG XP_006722067.1:p.Asp42Val
XM_006722004.3:c.125_126delinsTG XP_006722067.1:p.Asp42Val
XM_006722005.2:c.125_126delinsTG XP_006722068.1:p.Asp42Val
XM_006722005.3:c.125_126delinsTG XP_006722068.1:p.Asp42Val
XM_011525092.1:c.125_126delinsTG XP_011523394.1:p.Asp42Val
XM_011525092.2:c.125_126delinsTG XP_011523394.1:p.Asp42Val
XM_011525093.1:c.125_126delinsTG XP_011523395.1:p.Asp42Val
XM_011525093.2:c.125_126delinsTG XP_011523395.1:p.Asp42Val
XM_011525094.1:c.125_126delinsTG XP_011523396.1:p.Asp42Val
XM_011525094.2:c.125_126delinsTG XP_011523396.1:p.Asp42Val
XM_017024914.1:c.125_126delinsTG XP_016880403.1:p.Asp42Val
XM_017024915.1:c.125_126delinsTG XP_016880404.1:p.Asp42Val
XM_017024916.1:c.125_126delinsTG XP_016880405.1:p.Asp42Val
XM_017024917.1:c.125_126delinsTG XP_016880406.1:p.Asp42Val
XM_017024918.2:c.125_126delinsTG XP_016880407.1:p.Asp42Val
XM_017024919.1:c.125_126delinsTG XP_016880408.1:p.Asp42Val
XR_934513.1:n.549_550delinsTG
XR_934513.3:n.980_981delinsTG
XR_934514.1:n.549_550delinsTG
XR_934514.3:n.980_981delinsTG