Canonical Allele Identifier: CA3057243412
Community Standard Title: NM_058216.3(RAD51C):c.1033_1034delinsCC (p.Gly345Pro)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734124_58734125delinsCC , CM000679.2:g.58734124_58734125delinsCC GRCh38
NC_000017.10:g.56811485_56811486delinsCC , CM000679.1:g.56811485_56811486delinsCC GRCh37
NC_000017.9:g.54166484_54166485delinsCC NCBI36
NG_023199.1:g.46523_46524delinsCC , LRG_314:g.46523_46524delinsCC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1033_1034delinsCC MANE Select NP_478123.1:p.Gly345Pro
ENST00000337432.9:c.1033_1034delinsCC MANE Select ENSP00000336701.4:p.Gly345Pro
NM_058216.2:c.1033_1034delinsCC NP_478123.1:p.Gly345Pro
NR_103872.1:n.937_938delinsCC
NR_103872.2:n.908_909delinsCC
ENST00000337432.8:c.1033_1034delinsCC ENSP00000336701.4:p.Gly345Pro
ENST00000413590.5:c.674_675delinsCC
ENST00000461271.6:c.*1565_*1566delinsCC ENSP00000464056.2:n.*1565_*1566delinsCC
ENST00000461706.1:n.220_221delinsCC
ENST00000475762.5:c.*1669_*1670delinsCC ENSP00000432421.1:n.*1669_*1670delinsCC
ENST00000482007.5:c.*461_*462delinsCC ENSP00000433332.1:n.*461_*462delinsCC
ENST00000487525.5:c.*609_*610delinsCC ENSP00000431637.1:n.*609_*610delinsCC
ENST00000578151.1:n.246_247delinsCC
ENST00000581221.5:n.548_549delinsCC
ENST00000584804.1:c.267_268delinsCC ENSP00000463658.1:p.Arg89_Asp90delinsSerHis
ENST00000697680.1:c.*1997_*1998delinsCC ENSP00000513392.1:n.*1997_*1998delinsCC
ENST00000697681.1:c.*2194_*2195delinsCC ENSP00000513393.1:n.*2194_*2195delinsCC
ENST00000697683.1:c.*1969_*1970delinsCC ENSP00000513395.1:n.*1969_*1970delinsCC
ENST00000697685.1:c.*1730_*1731delinsCC ENSP00000513396.1:n.*1730_*1731delinsCC
ENST00000697686.1:c.804_805delinsCC ENSP00000513397.1:p.Arg268_Asp269delinsSerHis
ENST00000697689.1:c.*1447_*1448delinsCC ENSP00000513398.1:n.*1447_*1448delinsCC
ENST00000697690.1:c.911_912delinsCC ENSP00000513399.1:p.Gly304Ala
ENST00000697691.1:c.*1005_*1006delinsCC ENSP00000513400.1:n.*1005_*1006delinsCC
ENST00000697692.1:c.*1045_*1046delinsCC ENSP00000513401.1:n.*1045_*1046delinsCC
ENST00000697694.1:c.682_683delinsCC ENSP00000513402.1:p.Gly228Pro
ENST00000697695.1:n.1640_1641delinsCC
XM_006722001.2:c.1036_1037delinsCC XP_006722064.1:p.Gly346Pro
XM_006722001.4:c.1036_1037delinsCC XP_006722064.1:p.Gly346Pro
XM_006722002.2:c.972_973delinsCC XP_006722065.1:p.Arg324_Asp325delinsSerHis
XM_006722002.4:c.972_973delinsCC XP_006722065.1:p.Arg324_Asp325delinsSerHis
XM_006722004.2:c.685_686delinsCC XP_006722067.1:p.Gly229Pro
XM_006722004.3:c.685_686delinsCC XP_006722067.1:p.Gly229Pro
XM_006722005.2:c.685_686delinsCC XP_006722068.1:p.Gly229Pro
XM_006722005.3:c.685_686delinsCC XP_006722068.1:p.Gly229Pro
XM_011525092.1:c.685_686delinsCC XP_011523394.1:p.Gly229Pro
XM_011525092.2:c.685_686delinsCC XP_011523394.1:p.Gly229Pro
XM_011525093.1:c.685_686delinsCC XP_011523395.1:p.Gly229Pro
XM_011525093.2:c.685_686delinsCC XP_011523395.1:p.Gly229Pro
XM_011525094.1:c.685_686delinsCC XP_011523396.1:p.Gly229Pro
XM_011525094.2:c.685_686delinsCC XP_011523396.1:p.Gly229Pro
XM_017024914.1:c.682_683delinsCC XP_016880403.1:p.Gly228Pro
XM_017024915.1:c.682_683delinsCC XP_016880404.1:p.Gly228Pro
XM_017024916.1:c.682_683delinsCC XP_016880405.1:p.Gly228Pro
XM_017024917.1:c.682_683delinsCC XP_016880406.1:p.Gly228Pro
XM_017024918.2:c.682_683delinsCC XP_016880407.1:p.Gly228Pro
XM_017024919.1:c.621_622delinsCC XP_016880408.1:p.Arg207_Asp208delinsSerHis
XR_934513.1:n.1251_1252delinsCC
XR_934513.3:n.1682_1683delinsCC
XR_934514.1:n.1254_1255delinsCC
XR_934514.3:n.1685_1686delinsCC
XR_934886.1:n.149+3946_149+3947delinsGG
XR_934886.2:n.149+3946_149+3947delinsGG