Canonical Allele Identifier: CA3057243421
Community Standard Title: NM_058216.3(RAD51C):c.1065_1066delinsGC (p.Cys355_Ser356delinsTrpPro)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734156_58734157delinsGC , CM000679.2:g.58734156_58734157delinsGC GRCh38
NC_000017.10:g.56811517_56811518delinsGC , CM000679.1:g.56811517_56811518delinsGC GRCh37
NC_000017.9:g.54166516_54166517delinsGC NCBI36
NG_023199.1:g.46555_46556delinsGC , LRG_314:g.46555_46556delinsGC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1065_1066delinsGC MANE Select NP_478123.1:p.Cys355_Ser356delinsTrpPro
ENST00000337432.9:c.1065_1066delinsGC MANE Select ENSP00000336701.4:p.Cys355_Ser356delinsTrpPro
NM_058216.2:c.1065_1066delinsGC NP_478123.1:p.Cys355_Ser356delinsTrpPro
NR_103872.1:n.969_970delinsGC
NR_103872.2:n.940_941delinsGC
ENST00000337432.8:c.1065_1066delinsGC ENSP00000336701.4:p.Cys355_Ser356delinsTrpPro
ENST00000413590.5:c.706_707delinsGC
ENST00000461271.6:c.*1597_*1598delinsGC ENSP00000464056.2:n.*1597_*1598delinsGC
ENST00000461706.1:n.252_253delinsGC
ENST00000475762.5:c.*1701_*1702delinsGC ENSP00000432421.1:n.*1701_*1702delinsGC
ENST00000482007.5:c.*493_*494delinsGC ENSP00000433332.1:n.*493_*494delinsGC
ENST00000487525.5:c.*641_*642delinsGC ENSP00000431637.1:n.*641_*642delinsGC
ENST00000578151.1:n.278_279delinsGC
ENST00000581221.5:n.580_581delinsGC
ENST00000584804.1:c.299_300delinsGC ENSP00000463658.1:p.Val100Gly
ENST00000697680.1:c.*2029_*2030delinsGC ENSP00000513392.1:n.*2029_*2030delinsGC
ENST00000697681.1:c.*2226_*2227delinsGC ENSP00000513393.1:n.*2226_*2227delinsGC
ENST00000697683.1:c.*2001_*2002delinsGC ENSP00000513395.1:n.*2001_*2002delinsGC
ENST00000697685.1:c.*1762_*1763delinsGC ENSP00000513396.1:n.*1762_*1763delinsGC
ENST00000697686.1:c.836_837delinsGC ENSP00000513397.1:p.Val279Gly
ENST00000697689.1:c.*1479_*1480delinsGC ENSP00000513398.1:n.*1479_*1480delinsGC
ENST00000697690.1:c.*25_*26delinsGC ENSP00000513399.1:n.*25_*26delinsGC
ENST00000697691.1:c.*1037_*1038delinsGC ENSP00000513400.1:n.*1037_*1038delinsGC
ENST00000697692.1:c.*1077_*1078delinsGC ENSP00000513401.1:n.*1077_*1078delinsGC
ENST00000697694.1:c.714_715delinsGC ENSP00000513402.1:p.Cys238_Ser239delinsTrpPro
ENST00000697695.1:n.1672_1673delinsGC
XM_006722001.2:c.1068_1069delinsGC XP_006722064.1:p.Cys356_Ser357delinsTrpPro
XM_006722001.4:c.1068_1069delinsGC XP_006722064.1:p.Cys356_Ser357delinsTrpPro
XM_006722002.2:c.1004_1005delinsGC XP_006722065.1:p.Val335Gly
XM_006722002.4:c.1004_1005delinsGC XP_006722065.1:p.Val335Gly
XM_006722004.2:c.717_718delinsGC XP_006722067.1:p.Cys239_Ser240delinsTrpPro
XM_006722004.3:c.717_718delinsGC XP_006722067.1:p.Cys239_Ser240delinsTrpPro
XM_006722005.2:c.717_718delinsGC XP_006722068.1:p.Cys239_Ser240delinsTrpPro
XM_006722005.3:c.717_718delinsGC XP_006722068.1:p.Cys239_Ser240delinsTrpPro
XM_011525092.1:c.717_718delinsGC XP_011523394.1:p.Cys239_Ser240delinsTrpPro
XM_011525092.2:c.717_718delinsGC XP_011523394.1:p.Cys239_Ser240delinsTrpPro
XM_011525093.1:c.717_718delinsGC XP_011523395.1:p.Cys239_Ser240delinsTrpPro
XM_011525093.2:c.717_718delinsGC XP_011523395.1:p.Cys239_Ser240delinsTrpPro
XM_011525094.1:c.717_718delinsGC XP_011523396.1:p.Cys239_Ser240delinsTrpPro
XM_011525094.2:c.717_718delinsGC XP_011523396.1:p.Cys239_Ser240delinsTrpPro
XM_017024914.1:c.714_715delinsGC XP_016880403.1:p.Cys238_Ser239delinsTrpPro
XM_017024915.1:c.714_715delinsGC XP_016880404.1:p.Cys238_Ser239delinsTrpPro
XM_017024916.1:c.714_715delinsGC XP_016880405.1:p.Cys238_Ser239delinsTrpPro
XM_017024917.1:c.714_715delinsGC XP_016880406.1:p.Cys238_Ser239delinsTrpPro
XM_017024918.2:c.714_715delinsGC XP_016880407.1:p.Cys238_Ser239delinsTrpPro
XM_017024919.1:c.653_654delinsGC XP_016880408.1:p.Val218Gly
XR_934513.1:n.1283_1284delinsGC
XR_934513.3:n.1714_1715delinsGC
XR_934514.1:n.1286_1287delinsGC
XR_934514.3:n.1717_1718delinsGC
XR_934886.1:n.149+3914_149+3915delinsGC
XR_934886.2:n.149+3914_149+3915delinsGC