Canonical Allele Identifier: CA3060598413
Community Standard Title: NM_058216.3(RAD51C):c.776_777delinsGC (p.Thr259Ser)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709929_58709930delinsGC , CM000679.2:g.58709929_58709930delinsGC GRCh38
NC_000017.10:g.56787290_56787291delinsGC , CM000679.1:g.56787290_56787291delinsGC GRCh37
NC_000017.9:g.54142289_54142290delinsGC NCBI36
NG_023199.1:g.22328_22329delinsGC , LRG_314:g.22328_22329delinsGC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.776_777delinsGC MANE Select NP_478123.1:p.Thr259Ser
ENST00000337432.9:c.776_777delinsGC MANE Select ENSP00000336701.4:p.Thr259Ser
NM_058216.2:c.776_777delinsGC NP_478123.1:p.Thr259Ser
NR_103872.1:n.680_681delinsGC
NR_103872.2:n.651_652delinsGC
ENST00000337432.8:c.776_777delinsGC ENSP00000336701.4:p.Thr259Ser
ENST00000413590.5:c.414_415delinsGC
ENST00000461271.6:c.425_426delinsGC ENSP00000464056.2:p.Thr142Ser
ENST00000475762.5:c.*1479_*1480delinsGC ENSP00000432421.1:n.*1479_*1480delinsGC
ENST00000482007.5:c.*204_*205delinsGC ENSP00000433332.1:n.*204_*205delinsGC
ENST00000487525.5:c.*349_*350delinsGC ENSP00000431637.1:n.*349_*350delinsGC
ENST00000578151.1:n.111_112delinsGC
ENST00000581221.5:n.291_292delinsGC
ENST00000583539.5:c.776_777delinsGC ENSP00000463121.1:p.Thr259Ser
ENST00000584617.5:c.498_499delinsGC
ENST00000584804.1:c.71_72delinsGC ENSP00000463658.1:p.Thr24Ser
ENST00000697678.1:n.678_679delinsGC
ENST00000697679.1:n.1850_1851delinsGC
ENST00000697680.1:c.*1640_*1641delinsGC ENSP00000513392.1:n.*1640_*1641delinsGC
ENST00000697681.1:c.*1937_*1938delinsGC ENSP00000513393.1:n.*1937_*1938delinsGC
ENST00000697683.1:c.*1640_*1641delinsGC ENSP00000513395.1:n.*1640_*1641delinsGC
ENST00000697684.1:n.836_837delinsGC
ENST00000697685.1:c.*1473_*1474delinsGC ENSP00000513396.1:n.*1473_*1474delinsGC
ENST00000697686.1:c.425_426delinsGC ENSP00000513397.1:p.Thr142Ser
ENST00000697687.1:n.655_656delinsGC
ENST00000697688.1:n.822_823delinsGC
ENST00000697689.1:c.*1312_*1313delinsGC ENSP00000513398.1:n.*1312_*1313delinsGC
ENST00000697690.1:c.776_777delinsGC ENSP00000513399.1:p.Thr259Ser
ENST00000697691.1:c.*748_*749delinsGC ENSP00000513400.1:n.*748_*749delinsGC
ENST00000697692.1:c.*788_*789delinsGC ENSP00000513401.1:n.*788_*789delinsGC
ENST00000697694.1:c.425_426delinsGC ENSP00000513402.1:p.Thr142Ser
ENST00000697695.1:n.1383_1384delinsGC
XM_006722001.2:c.776_777delinsGC XP_006722064.1:p.Thr259Ser
XM_006722001.4:c.776_777delinsGC XP_006722064.1:p.Thr259Ser
XM_006722002.2:c.776_777delinsGC XP_006722065.1:p.Thr259Ser
XM_006722002.4:c.776_777delinsGC XP_006722065.1:p.Thr259Ser
XM_006722004.2:c.425_426delinsGC XP_006722067.1:p.Thr142Ser
XM_006722004.3:c.425_426delinsGC XP_006722067.1:p.Thr142Ser
XM_006722005.2:c.425_426delinsGC XP_006722068.1:p.Thr142Ser
XM_006722005.3:c.425_426delinsGC XP_006722068.1:p.Thr142Ser
XM_011525092.1:c.425_426delinsGC XP_011523394.1:p.Thr142Ser
XM_011525092.2:c.425_426delinsGC XP_011523394.1:p.Thr142Ser
XM_011525093.1:c.425_426delinsGC XP_011523395.1:p.Thr142Ser
XM_011525093.2:c.425_426delinsGC XP_011523395.1:p.Thr142Ser
XM_011525094.1:c.425_426delinsGC XP_011523396.1:p.Thr142Ser
XM_011525094.2:c.425_426delinsGC XP_011523396.1:p.Thr142Ser
XM_017024914.1:c.425_426delinsGC XP_016880403.1:p.Thr142Ser
XM_017024915.1:c.425_426delinsGC XP_016880404.1:p.Thr142Ser
XM_017024916.1:c.425_426delinsGC XP_016880405.1:p.Thr142Ser
XM_017024917.1:c.425_426delinsGC XP_016880406.1:p.Thr142Ser
XM_017024918.2:c.425_426delinsGC XP_016880407.1:p.Thr142Ser
XM_017024919.1:c.425_426delinsGC XP_016880408.1:p.Thr142Ser
XR_934513.1:n.994_995delinsGC
XR_934513.3:n.1425_1426delinsGC
XR_934514.1:n.994_995delinsGC
XR_934514.3:n.1425_1426delinsGC