Canonical Allele Identifier: CA3261179974
Community Standard Title: NM_058216.3(RAD51C):c.1051_1053delinsTTC (p.Val351Phe)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734142_58734144delinsTTC , CM000679.2:g.58734142_58734144delinsTTC GRCh38
NC_000017.10:g.56811503_56811505delinsTTC , CM000679.1:g.56811503_56811505delinsTTC GRCh37
NC_000017.9:g.54166502_54166504delinsTTC NCBI36
NG_023199.1:g.46541_46543delinsTTC , LRG_314:g.46541_46543delinsTTC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1051_1053delinsTTC MANE Select NP_478123.1:p.Val351Phe
ENST00000337432.9:c.1051_1053delinsTTC MANE Select ENSP00000336701.4:p.Val351Phe
NM_058216.2:c.1051_1053delinsTTC NP_478123.1:p.Val351Phe
NR_103872.1:n.955_957delinsTTC
NR_103872.2:n.926_928delinsTTC
ENST00000337432.8:c.1051_1053delinsTTC ENSP00000336701.4:p.Val351Phe
ENST00000413590.5:c.692_694delinsTTC
ENST00000461271.6:c.*1583_*1585delinsTTC ENSP00000464056.2:n.*1583_*1585delinsTTC
ENST00000461706.1:n.238_240delinsTTC
ENST00000475762.5:c.*1687_*1689delinsTTC ENSP00000432421.1:n.*1687_*1689delinsTTC
ENST00000482007.5:c.*479_*481delinsTTC ENSP00000433332.1:n.*479_*481delinsTTC
ENST00000487525.5:c.*627_*629delinsTTC ENSP00000431637.1:n.*627_*629delinsTTC
ENST00000578151.1:n.264_266delinsTTC
ENST00000581221.5:n.566_568delinsTTC
ENST00000584804.1:c.285_287delinsTTC ENSP00000463658.1:p.Leu95_Leu96delinsPheSer
ENST00000697680.1:c.*2015_*2017delinsTTC ENSP00000513392.1:n.*2015_*2017delinsTTC
ENST00000697681.1:c.*2212_*2214delinsTTC ENSP00000513393.1:n.*2212_*2214delinsTTC
ENST00000697683.1:c.*1987_*1989delinsTTC ENSP00000513395.1:n.*1987_*1989delinsTTC
ENST00000697685.1:c.*1748_*1750delinsTTC ENSP00000513396.1:n.*1748_*1750delinsTTC
ENST00000697686.1:c.822_824delinsTTC ENSP00000513397.1:p.Leu274_Leu275delinsPheSer
ENST00000697689.1:c.*1465_*1467delinsTTC ENSP00000513398.1:n.*1465_*1467delinsTTC
ENST00000697690.1:c.*11_*13delinsTTC ENSP00000513399.1:n.*11_*13delinsTTC
ENST00000697691.1:c.*1023_*1025delinsTTC ENSP00000513400.1:n.*1023_*1025delinsTTC
ENST00000697692.1:c.*1063_*1065delinsTTC ENSP00000513401.1:n.*1063_*1065delinsTTC
ENST00000697694.1:c.700_702delinsTTC ENSP00000513402.1:p.Val234Phe
ENST00000697695.1:n.1658_1660delinsTTC
XM_006722001.2:c.1054_1056delinsTTC XP_006722064.1:p.Val352Phe
XM_006722001.4:c.1054_1056delinsTTC XP_006722064.1:p.Val352Phe
XM_006722002.2:c.990_992delinsTTC XP_006722065.1:p.Leu330_Leu331delinsPheSer
XM_006722002.4:c.990_992delinsTTC XP_006722065.1:p.Leu330_Leu331delinsPheSer
XM_006722004.2:c.703_705delinsTTC XP_006722067.1:p.Val235Phe
XM_006722004.3:c.703_705delinsTTC XP_006722067.1:p.Val235Phe
XM_006722005.2:c.703_705delinsTTC XP_006722068.1:p.Val235Phe
XM_006722005.3:c.703_705delinsTTC XP_006722068.1:p.Val235Phe
XM_011525092.1:c.703_705delinsTTC XP_011523394.1:p.Val235Phe
XM_011525092.2:c.703_705delinsTTC XP_011523394.1:p.Val235Phe
XM_011525093.1:c.703_705delinsTTC XP_011523395.1:p.Val235Phe
XM_011525093.2:c.703_705delinsTTC XP_011523395.1:p.Val235Phe
XM_011525094.1:c.703_705delinsTTC XP_011523396.1:p.Val235Phe
XM_011525094.2:c.703_705delinsTTC XP_011523396.1:p.Val235Phe
XM_017024914.1:c.700_702delinsTTC XP_016880403.1:p.Val234Phe
XM_017024915.1:c.700_702delinsTTC XP_016880404.1:p.Val234Phe
XM_017024916.1:c.700_702delinsTTC XP_016880405.1:p.Val234Phe
XM_017024917.1:c.700_702delinsTTC XP_016880406.1:p.Val234Phe
XM_017024918.2:c.700_702delinsTTC XP_016880407.1:p.Val234Phe
XM_017024919.1:c.639_641delinsTTC XP_016880408.1:p.Leu213_Leu214delinsPheSer
XR_934513.1:n.1269_1271delinsTTC
XR_934513.3:n.1700_1702delinsTTC
XR_934514.1:n.1272_1274delinsTTC
XR_934514.3:n.1703_1705delinsTTC
XR_934886.1:n.149+3927_149+3929delinsGAA
XR_934886.2:n.149+3927_149+3929delinsGAA