Canonical Allele Identifier: CA3261179651
Community Standard Title: NM_058216.3(RAD51C):c.1033_1034delinsTA (p.Gly345Ter)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734124_58734125delinsTA , CM000679.2:g.58734124_58734125delinsTA GRCh38
NC_000017.10:g.56811485_56811486delinsTA , CM000679.1:g.56811485_56811486delinsTA GRCh37
NC_000017.9:g.54166484_54166485delinsTA NCBI36
NG_023199.1:g.46523_46524delinsTA , LRG_314:g.46523_46524delinsTA

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1033_1034delinsTA MANE Select NP_478123.1:p.Gly345Ter
ENST00000337432.9:c.1033_1034delinsTA MANE Select ENSP00000336701.4:p.Gly345Ter
NM_058216.2:c.1033_1034delinsTA NP_478123.1:p.Gly345Ter
NR_103872.1:n.937_938delinsTA
NR_103872.2:n.908_909delinsTA
ENST00000337432.8:c.1033_1034delinsTA ENSP00000336701.4:p.Gly345Ter
ENST00000413590.5:c.674_675delinsTA
ENST00000461271.6:c.*1565_*1566delinsTA ENSP00000464056.2:n.*1565_*1566delinsTA
ENST00000461706.1:n.220_221delinsTA
ENST00000475762.5:c.*1669_*1670delinsTA ENSP00000432421.1:n.*1669_*1670delinsTA
ENST00000482007.5:c.*461_*462delinsTA ENSP00000433332.1:n.*461_*462delinsTA
ENST00000487525.5:c.*609_*610delinsTA ENSP00000431637.1:n.*609_*610delinsTA
ENST00000578151.1:n.246_247delinsTA
ENST00000581221.5:n.548_549delinsTA
ENST00000584804.1:c.267_268delinsTA ENSP00000463658.1:p.Arg89_Asp90delinsSerAsn
ENST00000697680.1:c.*1997_*1998delinsTA ENSP00000513392.1:n.*1997_*1998delinsTA
ENST00000697681.1:c.*2194_*2195delinsTA ENSP00000513393.1:n.*2194_*2195delinsTA
ENST00000697683.1:c.*1969_*1970delinsTA ENSP00000513395.1:n.*1969_*1970delinsTA
ENST00000697685.1:c.*1730_*1731delinsTA ENSP00000513396.1:n.*1730_*1731delinsTA
ENST00000697686.1:c.804_805delinsTA ENSP00000513397.1:p.Arg268_Asp269delinsSerAsn
ENST00000697689.1:c.*1447_*1448delinsTA ENSP00000513398.1:n.*1447_*1448delinsTA
ENST00000697690.1:c.911_912delinsTA ENSP00000513399.1:p.Gly304Val
ENST00000697691.1:c.*1005_*1006delinsTA ENSP00000513400.1:n.*1005_*1006delinsTA
ENST00000697692.1:c.*1045_*1046delinsTA ENSP00000513401.1:n.*1045_*1046delinsTA
ENST00000697694.1:c.682_683delinsTA ENSP00000513402.1:p.Gly228Ter
ENST00000697695.1:n.1640_1641delinsTA
XM_006722001.2:c.1036_1037delinsTA XP_006722064.1:p.Gly346Ter
XM_006722001.4:c.1036_1037delinsTA XP_006722064.1:p.Gly346Ter
XM_006722002.2:c.972_973delinsTA XP_006722065.1:p.Arg324_Asp325delinsSerAsn
XM_006722002.4:c.972_973delinsTA XP_006722065.1:p.Arg324_Asp325delinsSerAsn
XM_006722004.2:c.685_686delinsTA XP_006722067.1:p.Gly229Ter
XM_006722004.3:c.685_686delinsTA XP_006722067.1:p.Gly229Ter
XM_006722005.2:c.685_686delinsTA XP_006722068.1:p.Gly229Ter
XM_006722005.3:c.685_686delinsTA XP_006722068.1:p.Gly229Ter
XM_011525092.1:c.685_686delinsTA XP_011523394.1:p.Gly229Ter
XM_011525092.2:c.685_686delinsTA XP_011523394.1:p.Gly229Ter
XM_011525093.1:c.685_686delinsTA XP_011523395.1:p.Gly229Ter
XM_011525093.2:c.685_686delinsTA XP_011523395.1:p.Gly229Ter
XM_011525094.1:c.685_686delinsTA XP_011523396.1:p.Gly229Ter
XM_011525094.2:c.685_686delinsTA XP_011523396.1:p.Gly229Ter
XM_017024914.1:c.682_683delinsTA XP_016880403.1:p.Gly228Ter
XM_017024915.1:c.682_683delinsTA XP_016880404.1:p.Gly228Ter
XM_017024916.1:c.682_683delinsTA XP_016880405.1:p.Gly228Ter
XM_017024917.1:c.682_683delinsTA XP_016880406.1:p.Gly228Ter
XM_017024918.2:c.682_683delinsTA XP_016880407.1:p.Gly228Ter
XM_017024919.1:c.621_622delinsTA XP_016880408.1:p.Arg207_Asp208delinsSerAsn
XR_934513.1:n.1251_1252delinsTA
XR_934513.3:n.1682_1683delinsTA
XR_934514.1:n.1254_1255delinsTA
XR_934514.3:n.1685_1686delinsTA
XR_934886.1:n.149+3946_149+3947delinsTA
XR_934886.2:n.149+3946_149+3947delinsTA