Canonical Allele Identifier: CA3261180648
Community Standard Title: NM_058216.3(RAD51C):c.427_429delinsAGA (p.Gln143Arg)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58696715_58696717delinsAGA , CM000679.2:g.58696715_58696717delinsAGA GRCh38
NC_000017.10:g.56774076_56774078delinsAGA , CM000679.1:g.56774076_56774078delinsAGA GRCh37
NC_000017.9:g.54129075_54129077delinsAGA NCBI36
NG_023199.1:g.9114_9116delinsAGA , LRG_314:g.9114_9116delinsAGA
NG_047169.1:g.363_365delinsTCT

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.427_429delinsAGA MANE Select NP_478123.1:p.Gln143Arg
ENST00000337432.9:c.427_429delinsAGA MANE Select ENSP00000336701.4:p.Gln143Arg
NM_058216.2:c.427_429delinsAGA NP_478123.1:p.Gln143Arg
NR_103872.1:n.475+1526_475+1528delinsAGA
NR_103872.2:n.446+1526_446+1528delinsAGA
ENST00000337432.8:c.427_429delinsAGA ENSP00000336701.4:p.Gln143Arg
ENST00000413590.5:c.65_67delinsAGA
ENST00000425173.5:c.223_225delinsAGA ENSP00000407282.1:p.Gln75Arg
ENST00000461271.5:c.76_78delinsAGA ENSP00000464056.1:p.Gln26Arg
ENST00000461271.6:c.76_78delinsAGA ENSP00000464056.2:p.Gln26Arg
ENST00000475762.5:c.*1130_*1132delinsAGA ENSP00000432421.1:n.*1130_*1132delinsAGA
ENST00000482007.5:c.404+1526_404+1528delinsAGA ENSP00000433332.1:n.404+1526_404+1528delinsAGA
ENST00000487525.5:c.404+1526_404+1528delinsAGA ENSP00000431637.1:n.404+1526_404+1528delinsAGA
ENST00000487921.5:n.339_341delinsAGA
ENST00000583539.5:c.427_429delinsAGA ENSP00000463121.1:p.Gln143Arg
ENST00000584617.5:c.149_151delinsAGA
ENST00000622327.4:c.163_165delinsAGA ENSP00000482326.1:p.Gln55Arg
ENST00000697675.1:n.3024_3026delinsAGA
ENST00000697676.1:n.487_489delinsAGA
ENST00000697677.1:n.1508_1510delinsAGA
ENST00000697678.1:n.329_331delinsAGA
ENST00000697679.1:n.1501_1503delinsAGA
ENST00000697680.1:c.*1291_*1293delinsAGA ENSP00000513392.1:n.*1291_*1293delinsAGA
ENST00000697681.1:c.*1318_*1320delinsAGA ENSP00000513393.1:n.*1318_*1320delinsAGA
ENST00000697683.1:c.*1291_*1293delinsAGA ENSP00000513395.1:n.*1291_*1293delinsAGA
ENST00000697684.1:n.487_489delinsAGA
ENST00000697685.1:c.*1268+1526_*1268+1528delinsAGA ENSP00000513396.1:n.*1268+1526_*1268+1528delinsAGA
ENST00000697686.1:c.76_78delinsAGA ENSP00000513397.1:p.Gln26Arg
ENST00000697687.1:n.450+1526_450+1528delinsAGA
ENST00000697688.1:n.473_475delinsAGA
ENST00000697689.1:c.*1107+1526_*1107+1528delinsAGA ENSP00000513398.1:n.*1107+1526_*1107+1528delinsAGA
ENST00000697690.1:c.427_429delinsAGA ENSP00000513399.1:p.Gln143Arg
ENST00000697691.1:c.*399_*401delinsAGA ENSP00000513400.1:n.*399_*401delinsAGA
ENST00000697692.1:c.*439_*441delinsAGA ENSP00000513401.1:n.*439_*441delinsAGA
ENST00000697694.1:c.76_78delinsAGA ENSP00000513402.1:p.Gln26Arg
ENST00000697695.1:n.1034_1036delinsAGA
XM_006722001.2:c.427_429delinsAGA XP_006722064.1:p.Gln143Arg
XM_006722001.4:c.427_429delinsAGA XP_006722064.1:p.Gln143Arg
XM_006722002.2:c.427_429delinsAGA XP_006722065.1:p.Gln143Arg
XM_006722002.4:c.427_429delinsAGA XP_006722065.1:p.Gln143Arg
XM_006722004.2:c.76_78delinsAGA XP_006722067.1:p.Gln26Arg
XM_006722004.3:c.76_78delinsAGA XP_006722067.1:p.Gln26Arg
XM_006722005.2:c.76_78delinsAGA XP_006722068.1:p.Gln26Arg
XM_006722005.3:c.76_78delinsAGA XP_006722068.1:p.Gln26Arg
XM_011525092.1:c.76_78delinsAGA XP_011523394.1:p.Gln26Arg
XM_011525092.2:c.76_78delinsAGA XP_011523394.1:p.Gln26Arg
XM_011525093.1:c.76_78delinsAGA XP_011523395.1:p.Gln26Arg
XM_011525093.2:c.76_78delinsAGA XP_011523395.1:p.Gln26Arg
XM_011525094.1:c.76_78delinsAGA XP_011523396.1:p.Gln26Arg
XM_011525094.2:c.76_78delinsAGA XP_011523396.1:p.Gln26Arg
XM_017024914.1:c.76_78delinsAGA XP_016880403.1:p.Gln26Arg
XM_017024915.1:c.76_78delinsAGA XP_016880404.1:p.Gln26Arg
XM_017024916.1:c.76_78delinsAGA XP_016880405.1:p.Gln26Arg
XM_017024917.1:c.76_78delinsAGA XP_016880406.1:p.Gln26Arg
XM_017024918.2:c.76_78delinsAGA XP_016880407.1:p.Gln26Arg
XM_017024919.1:c.76_78delinsAGA XP_016880408.1:p.Gln26Arg
XR_934513.1:n.500_502delinsAGA
XR_934513.3:n.931_933delinsAGA
XR_934514.1:n.500_502delinsAGA
XR_934514.3:n.931_933delinsAGA