Canonical Allele Identifier: CA3261179024
Community Standard Title: NM_058216.3(RAD51C):c.728_729delinsAC (p.Gly243Asp)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709881_58709882delinsAC , CM000679.2:g.58709881_58709882delinsAC GRCh38
NC_000017.10:g.56787242_56787243delinsAC , CM000679.1:g.56787242_56787243delinsAC GRCh37
NC_000017.9:g.54142241_54142242delinsAC NCBI36
NG_023199.1:g.22280_22281delinsAC , LRG_314:g.22280_22281delinsAC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.728_729delinsAC MANE Select NP_478123.1:p.Gly243Asp
ENST00000337432.9:c.728_729delinsAC MANE Select ENSP00000336701.4:p.Gly243Asp
NM_058216.2:c.728_729delinsAC NP_478123.1:p.Gly243Asp
NR_103872.1:n.632_633delinsAC
NR_103872.2:n.603_604delinsAC
ENST00000337432.8:c.728_729delinsAC ENSP00000336701.4:p.Gly243Asp
ENST00000413590.5:c.366_367delinsAC
ENST00000461271.5:c.377_378delinsAC ENSP00000464056.1:p.Gly126Asp
ENST00000461271.6:c.377_378delinsAC ENSP00000464056.2:p.Gly126Asp
ENST00000475762.5:c.*1431_*1432delinsAC ENSP00000432421.1:n.*1431_*1432delinsAC
ENST00000482007.5:c.*156_*157delinsAC ENSP00000433332.1:n.*156_*157delinsAC
ENST00000487525.5:c.*301_*302delinsAC ENSP00000431637.1:n.*301_*302delinsAC
ENST00000578151.1:n.63_64delinsAC
ENST00000581221.5:n.243_244delinsAC
ENST00000583539.5:c.728_729delinsAC ENSP00000463121.1:p.Gly243Asp
ENST00000584617.5:c.450_451delinsAC
ENST00000584804.1:c.23_24delinsAC ENSP00000463658.1:p.Gly8Asp
ENST00000697678.1:n.630_631delinsAC
ENST00000697679.1:n.1802_1803delinsAC
ENST00000697680.1:c.*1592_*1593delinsAC ENSP00000513392.1:n.*1592_*1593delinsAC
ENST00000697681.1:c.*1889_*1890delinsAC ENSP00000513393.1:n.*1889_*1890delinsAC
ENST00000697683.1:c.*1592_*1593delinsAC ENSP00000513395.1:n.*1592_*1593delinsAC
ENST00000697684.1:n.788_789delinsAC
ENST00000697685.1:c.*1425_*1426delinsAC ENSP00000513396.1:n.*1425_*1426delinsAC
ENST00000697686.1:c.377_378delinsAC ENSP00000513397.1:p.Gly126Asp
ENST00000697687.1:n.607_608delinsAC
ENST00000697688.1:n.774_775delinsAC
ENST00000697689.1:c.*1264_*1265delinsAC ENSP00000513398.1:n.*1264_*1265delinsAC
ENST00000697690.1:c.728_729delinsAC ENSP00000513399.1:p.Gly243Asp
ENST00000697691.1:c.*700_*701delinsAC ENSP00000513400.1:n.*700_*701delinsAC
ENST00000697692.1:c.*740_*741delinsAC ENSP00000513401.1:n.*740_*741delinsAC
ENST00000697694.1:c.377_378delinsAC ENSP00000513402.1:p.Gly126Asp
ENST00000697695.1:n.1335_1336delinsAC
XM_006722001.2:c.728_729delinsAC XP_006722064.1:p.Gly243Asp
XM_006722001.4:c.728_729delinsAC XP_006722064.1:p.Gly243Asp
XM_006722002.2:c.728_729delinsAC XP_006722065.1:p.Gly243Asp
XM_006722002.4:c.728_729delinsAC XP_006722065.1:p.Gly243Asp
XM_006722004.2:c.377_378delinsAC XP_006722067.1:p.Gly126Asp
XM_006722004.3:c.377_378delinsAC XP_006722067.1:p.Gly126Asp
XM_006722005.2:c.377_378delinsAC XP_006722068.1:p.Gly126Asp
XM_006722005.3:c.377_378delinsAC XP_006722068.1:p.Gly126Asp
XM_011525092.1:c.377_378delinsAC XP_011523394.1:p.Gly126Asp
XM_011525092.2:c.377_378delinsAC XP_011523394.1:p.Gly126Asp
XM_011525093.1:c.377_378delinsAC XP_011523395.1:p.Gly126Asp
XM_011525093.2:c.377_378delinsAC XP_011523395.1:p.Gly126Asp
XM_011525094.1:c.377_378delinsAC XP_011523396.1:p.Gly126Asp
XM_011525094.2:c.377_378delinsAC XP_011523396.1:p.Gly126Asp
XM_017024914.1:c.377_378delinsAC XP_016880403.1:p.Gly126Asp
XM_017024915.1:c.377_378delinsAC XP_016880404.1:p.Gly126Asp
XM_017024916.1:c.377_378delinsAC XP_016880405.1:p.Gly126Asp
XM_017024917.1:c.377_378delinsAC XP_016880406.1:p.Gly126Asp
XM_017024918.2:c.377_378delinsAC XP_016880407.1:p.Gly126Asp
XM_017024919.1:c.377_378delinsAC XP_016880408.1:p.Gly126Asp
XR_934513.1:n.946_947delinsAC
XR_934513.3:n.1377_1378delinsAC
XR_934514.1:n.946_947delinsAC
XR_934514.3:n.1377_1378delinsAC