Canonical Allele Identifier: CA3261180870
Community Standard Title: NM_058216.3(RAD51C):c.458_459delinsAC (p.Gly153Asp)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58696746_58696747delinsAC , CM000679.2:g.58696746_58696747delinsAC GRCh38
NC_000017.10:g.56774107_56774108delinsAC , CM000679.1:g.56774107_56774108delinsAC GRCh37
NC_000017.9:g.54129106_54129107delinsAC NCBI36
NG_023199.1:g.9145_9146delinsAC , LRG_314:g.9145_9146delinsAC
NG_047169.1:g.333_334delinsGT

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.458_459delinsAC MANE Select NP_478123.1:p.Gly153Asp
ENST00000337432.9:c.458_459delinsAC MANE Select ENSP00000336701.4:p.Gly153Asp
NM_058216.2:c.458_459delinsAC NP_478123.1:p.Gly153Asp
NR_103872.1:n.475+1557_475+1558delinsAC
NR_103872.2:n.446+1557_446+1558delinsAC
ENST00000337432.8:c.458_459delinsAC ENSP00000336701.4:p.Gly153Asp
ENST00000413590.5:c.96_97delinsAC
ENST00000425173.5:c.254_255delinsAC ENSP00000407282.1:p.Gly85Asp
ENST00000461271.5:c.107_108delinsAC ENSP00000464056.1:p.Gly36Asp
ENST00000461271.6:c.107_108delinsAC ENSP00000464056.2:p.Gly36Asp
ENST00000475762.5:c.*1161_*1162delinsAC ENSP00000432421.1:n.*1161_*1162delinsAC
ENST00000482007.5:c.404+1557_404+1558delinsAC ENSP00000433332.1:n.404+1557_404+1558delinsAC
ENST00000487525.5:c.404+1557_404+1558delinsAC ENSP00000431637.1:n.404+1557_404+1558delinsAC
ENST00000487921.5:n.370_371delinsAC
ENST00000583539.5:c.458_459delinsAC ENSP00000463121.1:p.Gly153Asp
ENST00000584617.5:c.180_181delinsAC
ENST00000622327.4:c.194_195delinsAC ENSP00000482326.1:p.Gly65Asp
ENST00000697675.1:n.3055_3056delinsAC
ENST00000697676.1:n.518_519delinsAC
ENST00000697677.1:n.1539_1540delinsAC
ENST00000697678.1:n.360_361delinsAC
ENST00000697679.1:n.1532_1533delinsAC
ENST00000697680.1:c.*1322_*1323delinsAC ENSP00000513392.1:n.*1322_*1323delinsAC
ENST00000697681.1:c.*1349_*1350delinsAC ENSP00000513393.1:n.*1349_*1350delinsAC
ENST00000697683.1:c.*1322_*1323delinsAC ENSP00000513395.1:n.*1322_*1323delinsAC
ENST00000697684.1:n.518_519delinsAC
ENST00000697685.1:c.*1268+1557_*1268+1558delinsAC ENSP00000513396.1:n.*1268+1557_*1268+1558delinsAC
ENST00000697686.1:c.107_108delinsAC ENSP00000513397.1:p.Gly36Asp
ENST00000697687.1:n.450+1557_450+1558delinsAC
ENST00000697688.1:n.504_505delinsAC
ENST00000697689.1:c.*1107+1557_*1107+1558delinsAC ENSP00000513398.1:n.*1107+1557_*1107+1558delinsAC
ENST00000697690.1:c.458_459delinsAC ENSP00000513399.1:p.Gly153Asp
ENST00000697691.1:c.*430_*431delinsAC ENSP00000513400.1:n.*430_*431delinsAC
ENST00000697692.1:c.*470_*471delinsAC ENSP00000513401.1:n.*470_*471delinsAC
ENST00000697694.1:c.107_108delinsAC ENSP00000513402.1:p.Gly36Asp
ENST00000697695.1:n.1065_1066delinsAC
XM_006722001.2:c.458_459delinsAC XP_006722064.1:p.Gly153Asp
XM_006722001.4:c.458_459delinsAC XP_006722064.1:p.Gly153Asp
XM_006722002.2:c.458_459delinsAC XP_006722065.1:p.Gly153Asp
XM_006722002.4:c.458_459delinsAC XP_006722065.1:p.Gly153Asp
XM_006722004.2:c.107_108delinsAC XP_006722067.1:p.Gly36Asp
XM_006722004.3:c.107_108delinsAC XP_006722067.1:p.Gly36Asp
XM_006722005.2:c.107_108delinsAC XP_006722068.1:p.Gly36Asp
XM_006722005.3:c.107_108delinsAC XP_006722068.1:p.Gly36Asp
XM_011525092.1:c.107_108delinsAC XP_011523394.1:p.Gly36Asp
XM_011525092.2:c.107_108delinsAC XP_011523394.1:p.Gly36Asp
XM_011525093.1:c.107_108delinsAC XP_011523395.1:p.Gly36Asp
XM_011525093.2:c.107_108delinsAC XP_011523395.1:p.Gly36Asp
XM_011525094.1:c.107_108delinsAC XP_011523396.1:p.Gly36Asp
XM_011525094.2:c.107_108delinsAC XP_011523396.1:p.Gly36Asp
XM_017024914.1:c.107_108delinsAC XP_016880403.1:p.Gly36Asp
XM_017024915.1:c.107_108delinsAC XP_016880404.1:p.Gly36Asp
XM_017024916.1:c.107_108delinsAC XP_016880405.1:p.Gly36Asp
XM_017024917.1:c.107_108delinsAC XP_016880406.1:p.Gly36Asp
XM_017024918.2:c.107_108delinsAC XP_016880407.1:p.Gly36Asp
XM_017024919.1:c.107_108delinsAC XP_016880408.1:p.Gly36Asp
XR_934513.1:n.531_532delinsAC
XR_934513.3:n.962_963delinsAC
XR_934514.1:n.531_532delinsAC
XR_934514.3:n.962_963delinsAC