Canonical Allele Identifier: CA3261179751
Community Standard Title: NM_058216.3(RAD51C):c.775_777delinsGCC (p.Thr259Ala)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709928_58709930delinsGCC , CM000679.2:g.58709928_58709930delinsGCC GRCh38
NC_000017.10:g.56787289_56787291delinsGCC , CM000679.1:g.56787289_56787291delinsGCC GRCh37
NC_000017.9:g.54142288_54142290delinsGCC NCBI36
NG_023199.1:g.22327_22329delinsGCC , LRG_314:g.22327_22329delinsGCC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.775_777delinsGCC MANE Select NP_478123.1:p.Thr259Ala
ENST00000337432.9:c.775_777delinsGCC MANE Select ENSP00000336701.4:p.Thr259Ala
NM_058216.2:c.775_777delinsGCC NP_478123.1:p.Thr259Ala
NR_103872.1:n.679_681delinsGCC
NR_103872.2:n.650_652delinsGCC
ENST00000337432.8:c.775_777delinsGCC ENSP00000336701.4:p.Thr259Ala
ENST00000413590.5:c.413_415delinsGCC
ENST00000461271.6:c.424_426delinsGCC ENSP00000464056.2:p.Thr142Ala
ENST00000475762.5:c.*1478_*1480delinsGCC ENSP00000432421.1:n.*1478_*1480delinsGCC
ENST00000482007.5:c.*203_*205delinsGCC ENSP00000433332.1:n.*203_*205delinsGCC
ENST00000487525.5:c.*348_*350delinsGCC ENSP00000431637.1:n.*348_*350delinsGCC
ENST00000578151.1:n.110_112delinsGCC
ENST00000581221.5:n.290_292delinsGCC
ENST00000583539.5:c.775_777delinsGCC ENSP00000463121.1:p.Thr259Ala
ENST00000584617.5:c.497_499delinsGCC
ENST00000584804.1:c.70_72delinsGCC ENSP00000463658.1:p.Thr24Ala
ENST00000697678.1:n.677_679delinsGCC
ENST00000697679.1:n.1849_1851delinsGCC
ENST00000697680.1:c.*1639_*1641delinsGCC ENSP00000513392.1:n.*1639_*1641delinsGCC
ENST00000697681.1:c.*1936_*1938delinsGCC ENSP00000513393.1:n.*1936_*1938delinsGCC
ENST00000697683.1:c.*1639_*1641delinsGCC ENSP00000513395.1:n.*1639_*1641delinsGCC
ENST00000697684.1:n.835_837delinsGCC
ENST00000697685.1:c.*1472_*1474delinsGCC ENSP00000513396.1:n.*1472_*1474delinsGCC
ENST00000697686.1:c.424_426delinsGCC ENSP00000513397.1:p.Thr142Ala
ENST00000697687.1:n.654_656delinsGCC
ENST00000697688.1:n.821_823delinsGCC
ENST00000697689.1:c.*1311_*1313delinsGCC ENSP00000513398.1:n.*1311_*1313delinsGCC
ENST00000697690.1:c.775_777delinsGCC ENSP00000513399.1:p.Thr259Ala
ENST00000697691.1:c.*747_*749delinsGCC ENSP00000513400.1:n.*747_*749delinsGCC
ENST00000697692.1:c.*787_*789delinsGCC ENSP00000513401.1:n.*787_*789delinsGCC
ENST00000697694.1:c.424_426delinsGCC ENSP00000513402.1:p.Thr142Ala
ENST00000697695.1:n.1382_1384delinsGCC
XM_006722001.2:c.775_777delinsGCC XP_006722064.1:p.Thr259Ala
XM_006722001.4:c.775_777delinsGCC XP_006722064.1:p.Thr259Ala
XM_006722002.2:c.775_777delinsGCC XP_006722065.1:p.Thr259Ala
XM_006722002.4:c.775_777delinsGCC XP_006722065.1:p.Thr259Ala
XM_006722004.2:c.424_426delinsGCC XP_006722067.1:p.Thr142Ala
XM_006722004.3:c.424_426delinsGCC XP_006722067.1:p.Thr142Ala
XM_006722005.2:c.424_426delinsGCC XP_006722068.1:p.Thr142Ala
XM_006722005.3:c.424_426delinsGCC XP_006722068.1:p.Thr142Ala
XM_011525092.1:c.424_426delinsGCC XP_011523394.1:p.Thr142Ala
XM_011525092.2:c.424_426delinsGCC XP_011523394.1:p.Thr142Ala
XM_011525093.1:c.424_426delinsGCC XP_011523395.1:p.Thr142Ala
XM_011525093.2:c.424_426delinsGCC XP_011523395.1:p.Thr142Ala
XM_011525094.1:c.424_426delinsGCC XP_011523396.1:p.Thr142Ala
XM_011525094.2:c.424_426delinsGCC XP_011523396.1:p.Thr142Ala
XM_017024914.1:c.424_426delinsGCC XP_016880403.1:p.Thr142Ala
XM_017024915.1:c.424_426delinsGCC XP_016880404.1:p.Thr142Ala
XM_017024916.1:c.424_426delinsGCC XP_016880405.1:p.Thr142Ala
XM_017024917.1:c.424_426delinsGCC XP_016880406.1:p.Thr142Ala
XM_017024918.2:c.424_426delinsGCC XP_016880407.1:p.Thr142Ala
XM_017024919.1:c.424_426delinsGCC XP_016880408.1:p.Thr142Ala
XR_934513.1:n.993_995delinsGCC
XR_934513.3:n.1424_1426delinsGCC
XR_934514.1:n.993_995delinsGCC
XR_934514.3:n.1424_1426delinsGCC