Canonical Allele Identifier: CA3261180328
Community Standard Title: NM_058216.3(RAD51C):c.1072_1074del (p.Gln358del)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734163_58734165del , CM000679.2:g.58734163_58734165del GRCh38
NC_000017.10:g.56811524_56811526del , CM000679.1:g.56811524_56811526del GRCh37
NC_000017.9:g.54166523_54166525del NCBI36
NG_023199.1:g.46562_46564del , LRG_314:g.46562_46564del

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1072_1074del MANE Select NP_478123.1:p.Gln358del
ENST00000337432.9:c.1072_1074del MANE Select ENSP00000336701.4:p.Gln358del
NM_058216.2:c.1072_1074del NP_478123.1:p.Gln358del
NR_103872.1:n.976_978del
NR_103872.2:n.947_949del
ENST00000337432.8:c.1072_1074del ENSP00000336701.4:p.Gln358del
ENST00000413590.5:c.713_715del
ENST00000461271.6:c.*1604_*1606del ENSP00000464056.2:n.*1604_*1606del
ENST00000461706.1:n.259_261del
ENST00000475762.5:c.*1708_*1710del ENSP00000432421.1:n.*1708_*1710del
ENST00000482007.5:c.*500_*502del ENSP00000433332.1:n.*500_*502del
ENST00000487525.5:c.*648_*650del ENSP00000431637.1:n.*648_*650del
ENST00000578151.1:n.285_287del
ENST00000581221.5:n.587_589del
ENST00000584804.1:c.306_308del ENSP00000463658.1:p.Cys102Ter
ENST00000697680.1:c.*2036_*2038del ENSP00000513392.1:n.*2036_*2038del
ENST00000697681.1:c.*2233_*2235del ENSP00000513393.1:n.*2233_*2235del
ENST00000697683.1:c.*2008_*2010del ENSP00000513395.1:n.*2008_*2010del
ENST00000697685.1:c.*1769_*1771del ENSP00000513396.1:n.*1769_*1771del
ENST00000697686.1:c.843_845del ENSP00000513397.1:p.Cys281Ter
ENST00000697689.1:c.*1486_*1488del ENSP00000513398.1:n.*1486_*1488del
ENST00000697690.1:c.*32_*34del ENSP00000513399.1:n.*32_*34del
ENST00000697691.1:c.*1044_*1046del ENSP00000513400.1:n.*1044_*1046del
ENST00000697692.1:c.*1084_*1086del ENSP00000513401.1:n.*1084_*1086del
ENST00000697694.1:c.721_723del ENSP00000513402.1:p.Gln241del
ENST00000697695.1:n.1679_1681del
XM_006722001.2:c.1075_1077del XP_006722064.1:p.Gln359del
XM_006722001.4:c.1075_1077del XP_006722064.1:p.Gln359del
XM_006722002.2:c.1011_1013del XP_006722065.1:p.Cys337Ter
XM_006722002.4:c.1011_1013del XP_006722065.1:p.Cys337Ter
XM_006722004.2:c.724_726del XP_006722067.1:p.Gln242del
XM_006722004.3:c.724_726del XP_006722067.1:p.Gln242del
XM_006722005.2:c.724_726del XP_006722068.1:p.Gln242del
XM_006722005.3:c.724_726del XP_006722068.1:p.Gln242del
XM_011525092.1:c.724_726del XP_011523394.1:p.Gln242del
XM_011525092.2:c.724_726del XP_011523394.1:p.Gln242del
XM_011525093.1:c.724_726del XP_011523395.1:p.Gln242del
XM_011525093.2:c.724_726del XP_011523395.1:p.Gln242del
XM_011525094.1:c.724_726del XP_011523396.1:p.Gln242del
XM_011525094.2:c.724_726del XP_011523396.1:p.Gln242del
XM_017024914.1:c.721_723del XP_016880403.1:p.Gln241del
XM_017024915.1:c.721_723del XP_016880404.1:p.Gln241del
XM_017024916.1:c.721_723del XP_016880405.1:p.Gln241del
XM_017024917.1:c.721_723del XP_016880406.1:p.Gln241del
XM_017024918.2:c.721_723del XP_016880407.1:p.Gln241del
XM_017024919.1:c.660_662del XP_016880408.1:p.Cys220Ter
XR_934513.1:n.1290_1292del
XR_934513.3:n.1721_1723del
XR_934514.1:n.1293_1295del
XR_934514.3:n.1724_1726del
XR_934886.1:n.149+3906_149+3908del
XR_934886.2:n.149+3906_149+3908del