Canonical Allele Identifier: CA3261180389
Community Standard Title: NM_058216.3(RAD51C):c.406_408delinsGTC (p.Met136Val)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58696694_58696696delinsGTC , CM000679.2:g.58696694_58696696delinsGTC GRCh38
NC_000017.10:g.56774055_56774057delinsGTC , CM000679.1:g.56774055_56774057delinsGTC GRCh37
NC_000017.9:g.54129054_54129056delinsGTC NCBI36
NG_023199.1:g.9093_9095delinsGTC , LRG_314:g.9093_9095delinsGTC
NG_047169.1:g.384_386delinsGAC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.406_408delinsGTC MANE Select NP_478123.1:p.Met136Val
ENST00000337432.9:c.406_408delinsGTC MANE Select ENSP00000336701.4:p.Met136Val
NM_058216.2:c.406_408delinsGTC NP_478123.1:p.Met136Val
NR_103872.1:n.475+1505_475+1507delinsGTC
NR_103872.2:n.446+1505_446+1507delinsGTC
ENST00000337432.8:c.406_408delinsGTC ENSP00000336701.4:p.Met136Val
ENST00000413590.5:c.44_46delinsGTC
ENST00000425173.5:c.202_204delinsGTC ENSP00000407282.1:p.Met68Val
ENST00000461271.5:c.55_57delinsGTC ENSP00000464056.1:p.Met19Val
ENST00000461271.6:c.55_57delinsGTC ENSP00000464056.2:p.Met19Val
ENST00000475762.5:c.*1109_*1111delinsGTC ENSP00000432421.1:n.*1109_*1111delinsGTC
ENST00000482007.5:c.404+1505_404+1507delinsGTC ENSP00000433332.1:n.404+1505_404+1507delinsGTC
ENST00000487525.5:c.404+1505_404+1507delinsGTC ENSP00000431637.1:n.404+1505_404+1507delinsGTC
ENST00000487921.5:n.318_320delinsGTC
ENST00000583539.5:c.406_408delinsGTC ENSP00000463121.1:p.Met136Val
ENST00000584617.5:c.128_130delinsGTC
ENST00000622327.4:c.142_144delinsGTC ENSP00000482326.1:p.Met48Val
ENST00000697675.1:n.3003_3005delinsGTC
ENST00000697676.1:n.466_468delinsGTC
ENST00000697677.1:n.1487_1489delinsGTC
ENST00000697678.1:n.308_310delinsGTC
ENST00000697679.1:n.1480_1482delinsGTC
ENST00000697680.1:c.*1270_*1272delinsGTC ENSP00000513392.1:n.*1270_*1272delinsGTC
ENST00000697681.1:c.*1297_*1299delinsGTC ENSP00000513393.1:n.*1297_*1299delinsGTC
ENST00000697683.1:c.*1270_*1272delinsGTC ENSP00000513395.1:n.*1270_*1272delinsGTC
ENST00000697684.1:n.466_468delinsGTC
ENST00000697685.1:c.*1268+1505_*1268+1507delinsGTC ENSP00000513396.1:n.*1268+1505_*1268+1507delinsGTC
ENST00000697686.1:c.55_57delinsGTC ENSP00000513397.1:p.Met19Val
ENST00000697687.1:n.450+1505_450+1507delinsGTC
ENST00000697688.1:n.452_454delinsGTC
ENST00000697689.1:c.*1107+1505_*1107+1507delinsGTC ENSP00000513398.1:n.*1107+1505_*1107+1507delinsGTC
ENST00000697690.1:c.406_408delinsGTC ENSP00000513399.1:p.Met136Val
ENST00000697691.1:c.*378_*380delinsGTC ENSP00000513400.1:n.*378_*380delinsGTC
ENST00000697692.1:c.*418_*420delinsGTC ENSP00000513401.1:n.*418_*420delinsGTC
ENST00000697694.1:c.55_57delinsGTC ENSP00000513402.1:p.Met19Val
ENST00000697695.1:n.1013_1015delinsGTC
XM_006722001.2:c.406_408delinsGTC XP_006722064.1:p.Met136Val
XM_006722001.4:c.406_408delinsGTC XP_006722064.1:p.Met136Val
XM_006722002.2:c.406_408delinsGTC XP_006722065.1:p.Met136Val
XM_006722002.4:c.406_408delinsGTC XP_006722065.1:p.Met136Val
XM_006722004.2:c.55_57delinsGTC XP_006722067.1:p.Met19Val
XM_006722004.3:c.55_57delinsGTC XP_006722067.1:p.Met19Val
XM_006722005.2:c.55_57delinsGTC XP_006722068.1:p.Met19Val
XM_006722005.3:c.55_57delinsGTC XP_006722068.1:p.Met19Val
XM_011525092.1:c.55_57delinsGTC XP_011523394.1:p.Met19Val
XM_011525092.2:c.55_57delinsGTC XP_011523394.1:p.Met19Val
XM_011525093.1:c.55_57delinsGTC XP_011523395.1:p.Met19Val
XM_011525093.2:c.55_57delinsGTC XP_011523395.1:p.Met19Val
XM_011525094.1:c.55_57delinsGTC XP_011523396.1:p.Met19Val
XM_011525094.2:c.55_57delinsGTC XP_011523396.1:p.Met19Val
XM_017024914.1:c.55_57delinsGTC XP_016880403.1:p.Met19Val
XM_017024915.1:c.55_57delinsGTC XP_016880404.1:p.Met19Val
XM_017024916.1:c.55_57delinsGTC XP_016880405.1:p.Met19Val
XM_017024917.1:c.55_57delinsGTC XP_016880406.1:p.Met19Val
XM_017024918.2:c.55_57delinsGTC XP_016880407.1:p.Met19Val
XM_017024919.1:c.55_57delinsGTC XP_016880408.1:p.Met19Val
XR_934513.1:n.479_481delinsGTC
XR_934513.3:n.910_912delinsGTC
XR_934514.1:n.479_481delinsGTC
XR_934514.3:n.910_912delinsGTC