Canonical Allele Identifier: CA3057243493
Community Standard Title: NM_058216.3(RAD51C):c.1033_1034delinsTC (p.Gly345Ser)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734124_58734125delinsTC , CM000679.2:g.58734124_58734125delinsTC GRCh38
NC_000017.10:g.56811485_56811486delinsTC , CM000679.1:g.56811485_56811486delinsTC GRCh37
NC_000017.9:g.54166484_54166485delinsTC NCBI36
NG_023199.1:g.46523_46524delinsTC , LRG_314:g.46523_46524delinsTC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1033_1034delinsTC MANE Select NP_478123.1:p.Gly345Ser
ENST00000337432.9:c.1033_1034delinsTC MANE Select ENSP00000336701.4:p.Gly345Ser
NM_058216.2:c.1033_1034delinsTC NP_478123.1:p.Gly345Ser
NR_103872.1:n.937_938delinsTC
NR_103872.2:n.908_909delinsTC
ENST00000337432.8:c.1033_1034delinsTC ENSP00000336701.4:p.Gly345Ser
ENST00000413590.5:c.674_675delinsTC
ENST00000461271.6:c.*1565_*1566delinsTC ENSP00000464056.2:n.*1565_*1566delinsTC
ENST00000461706.1:n.220_221delinsTC
ENST00000475762.5:c.*1669_*1670delinsTC ENSP00000432421.1:n.*1669_*1670delinsTC
ENST00000482007.5:c.*461_*462delinsTC ENSP00000433332.1:n.*461_*462delinsTC
ENST00000487525.5:c.*609_*610delinsTC ENSP00000431637.1:n.*609_*610delinsTC
ENST00000578151.1:n.246_247delinsTC
ENST00000581221.5:n.548_549delinsTC
ENST00000584804.1:c.267_268delinsTC ENSP00000463658.1:p.Arg89_Asp90delinsSerHis
ENST00000697680.1:c.*1997_*1998delinsTC ENSP00000513392.1:n.*1997_*1998delinsTC
ENST00000697681.1:c.*2194_*2195delinsTC ENSP00000513393.1:n.*2194_*2195delinsTC
ENST00000697683.1:c.*1969_*1970delinsTC ENSP00000513395.1:n.*1969_*1970delinsTC
ENST00000697685.1:c.*1730_*1731delinsTC ENSP00000513396.1:n.*1730_*1731delinsTC
ENST00000697686.1:c.804_805delinsTC ENSP00000513397.1:p.Arg268_Asp269delinsSerHis
ENST00000697689.1:c.*1447_*1448delinsTC ENSP00000513398.1:n.*1447_*1448delinsTC
ENST00000697690.1:c.911_912delinsTC ENSP00000513399.1:p.Gly304Val
ENST00000697691.1:c.*1005_*1006delinsTC ENSP00000513400.1:n.*1005_*1006delinsTC
ENST00000697692.1:c.*1045_*1046delinsTC ENSP00000513401.1:n.*1045_*1046delinsTC
ENST00000697694.1:c.682_683delinsTC ENSP00000513402.1:p.Gly228Ser
ENST00000697695.1:n.1640_1641delinsTC
XM_006722001.2:c.1036_1037delinsTC XP_006722064.1:p.Gly346Ser
XM_006722001.4:c.1036_1037delinsTC XP_006722064.1:p.Gly346Ser
XM_006722002.2:c.972_973delinsTC XP_006722065.1:p.Arg324_Asp325delinsSerHis
XM_006722002.4:c.972_973delinsTC XP_006722065.1:p.Arg324_Asp325delinsSerHis
XM_006722004.2:c.685_686delinsTC XP_006722067.1:p.Gly229Ser
XM_006722004.3:c.685_686delinsTC XP_006722067.1:p.Gly229Ser
XM_006722005.2:c.685_686delinsTC XP_006722068.1:p.Gly229Ser
XM_006722005.3:c.685_686delinsTC XP_006722068.1:p.Gly229Ser
XM_011525092.1:c.685_686delinsTC XP_011523394.1:p.Gly229Ser
XM_011525092.2:c.685_686delinsTC XP_011523394.1:p.Gly229Ser
XM_011525093.1:c.685_686delinsTC XP_011523395.1:p.Gly229Ser
XM_011525093.2:c.685_686delinsTC XP_011523395.1:p.Gly229Ser
XM_011525094.1:c.685_686delinsTC XP_011523396.1:p.Gly229Ser
XM_011525094.2:c.685_686delinsTC XP_011523396.1:p.Gly229Ser
XM_017024914.1:c.682_683delinsTC XP_016880403.1:p.Gly228Ser
XM_017024915.1:c.682_683delinsTC XP_016880404.1:p.Gly228Ser
XM_017024916.1:c.682_683delinsTC XP_016880405.1:p.Gly228Ser
XM_017024917.1:c.682_683delinsTC XP_016880406.1:p.Gly228Ser
XM_017024918.2:c.682_683delinsTC XP_016880407.1:p.Gly228Ser
XM_017024919.1:c.621_622delinsTC XP_016880408.1:p.Arg207_Asp208delinsSerHis
XR_934513.1:n.1251_1252delinsTC
XR_934513.3:n.1682_1683delinsTC
XR_934514.1:n.1254_1255delinsTC
XR_934514.3:n.1685_1686delinsTC
XR_934886.1:n.149+3946_149+3947delinsGA
XR_934886.2:n.149+3946_149+3947delinsGA