Canonical Allele Identifier: CA3057243522
Community Standard Title: NM_058216.3(RAD51C):c.1065_1066delinsGG (p.Cys355_Ser356delinsTrpAla)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734156_58734157delinsGG , CM000679.2:g.58734156_58734157delinsGG GRCh38
NC_000017.10:g.56811517_56811518delinsGG , CM000679.1:g.56811517_56811518delinsGG GRCh37
NC_000017.9:g.54166516_54166517delinsGG NCBI36
NG_023199.1:g.46555_46556delinsGG , LRG_314:g.46555_46556delinsGG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1065_1066delinsGG MANE Select NP_478123.1:p.Cys355_Ser356delinsTrpAla
ENST00000337432.9:c.1065_1066delinsGG MANE Select ENSP00000336701.4:p.Cys355_Ser356delinsTrpAla
NM_058216.2:c.1065_1066delinsGG NP_478123.1:p.Cys355_Ser356delinsTrpAla
NR_103872.1:n.969_970delinsGG
NR_103872.2:n.940_941delinsGG
ENST00000337432.8:c.1065_1066delinsGG ENSP00000336701.4:p.Cys355_Ser356delinsTrpAla
ENST00000413590.5:c.706_707delinsGG
ENST00000461271.6:c.*1597_*1598delinsGG ENSP00000464056.2:n.*1597_*1598delinsGG
ENST00000461706.1:n.252_253delinsGG
ENST00000475762.5:c.*1701_*1702delinsGG ENSP00000432421.1:n.*1701_*1702delinsGG
ENST00000482007.5:c.*493_*494delinsGG ENSP00000433332.1:n.*493_*494delinsGG
ENST00000487525.5:c.*641_*642delinsGG ENSP00000431637.1:n.*641_*642delinsGG
ENST00000578151.1:n.278_279delinsGG
ENST00000581221.5:n.580_581delinsGG
ENST00000584804.1:c.299_300delinsGG ENSP00000463658.1:p.Val100Gly
ENST00000697680.1:c.*2029_*2030delinsGG ENSP00000513392.1:n.*2029_*2030delinsGG
ENST00000697681.1:c.*2226_*2227delinsGG ENSP00000513393.1:n.*2226_*2227delinsGG
ENST00000697683.1:c.*2001_*2002delinsGG ENSP00000513395.1:n.*2001_*2002delinsGG
ENST00000697685.1:c.*1762_*1763delinsGG ENSP00000513396.1:n.*1762_*1763delinsGG
ENST00000697686.1:c.836_837delinsGG ENSP00000513397.1:p.Val279Gly
ENST00000697689.1:c.*1479_*1480delinsGG ENSP00000513398.1:n.*1479_*1480delinsGG
ENST00000697690.1:c.*25_*26delinsGG ENSP00000513399.1:n.*25_*26delinsGG
ENST00000697691.1:c.*1037_*1038delinsGG ENSP00000513400.1:n.*1037_*1038delinsGG
ENST00000697692.1:c.*1077_*1078delinsGG ENSP00000513401.1:n.*1077_*1078delinsGG
ENST00000697694.1:c.714_715delinsGG ENSP00000513402.1:p.Cys238_Ser239delinsTrpAla
ENST00000697695.1:n.1672_1673delinsGG
XM_006722001.2:c.1068_1069delinsGG XP_006722064.1:p.Cys356_Ser357delinsTrpAla
XM_006722001.4:c.1068_1069delinsGG XP_006722064.1:p.Cys356_Ser357delinsTrpAla
XM_006722002.2:c.1004_1005delinsGG XP_006722065.1:p.Val335Gly
XM_006722002.4:c.1004_1005delinsGG XP_006722065.1:p.Val335Gly
XM_006722004.2:c.717_718delinsGG XP_006722067.1:p.Cys239_Ser240delinsTrpAla
XM_006722004.3:c.717_718delinsGG XP_006722067.1:p.Cys239_Ser240delinsTrpAla
XM_006722005.2:c.717_718delinsGG XP_006722068.1:p.Cys239_Ser240delinsTrpAla
XM_006722005.3:c.717_718delinsGG XP_006722068.1:p.Cys239_Ser240delinsTrpAla
XM_011525092.1:c.717_718delinsGG XP_011523394.1:p.Cys239_Ser240delinsTrpAla
XM_011525092.2:c.717_718delinsGG XP_011523394.1:p.Cys239_Ser240delinsTrpAla
XM_011525093.1:c.717_718delinsGG XP_011523395.1:p.Cys239_Ser240delinsTrpAla
XM_011525093.2:c.717_718delinsGG XP_011523395.1:p.Cys239_Ser240delinsTrpAla
XM_011525094.1:c.717_718delinsGG XP_011523396.1:p.Cys239_Ser240delinsTrpAla
XM_011525094.2:c.717_718delinsGG XP_011523396.1:p.Cys239_Ser240delinsTrpAla
XM_017024914.1:c.714_715delinsGG XP_016880403.1:p.Cys238_Ser239delinsTrpAla
XM_017024915.1:c.714_715delinsGG XP_016880404.1:p.Cys238_Ser239delinsTrpAla
XM_017024916.1:c.714_715delinsGG XP_016880405.1:p.Cys238_Ser239delinsTrpAla
XM_017024917.1:c.714_715delinsGG XP_016880406.1:p.Cys238_Ser239delinsTrpAla
XM_017024918.2:c.714_715delinsGG XP_016880407.1:p.Cys238_Ser239delinsTrpAla
XM_017024919.1:c.653_654delinsGG XP_016880408.1:p.Val218Gly
XR_934513.1:n.1283_1284delinsGG
XR_934513.3:n.1714_1715delinsGG
XR_934514.1:n.1286_1287delinsGG
XR_934514.3:n.1717_1718delinsGG
XR_934886.1:n.149+3914_149+3915delinsCC
XR_934886.2:n.149+3914_149+3915delinsCC