Canonical Allele Identifier: CA3261179978
Community Standard Title: NM_058216.3(RAD51C):c.1051_1053delinsCTG (p.Val351Leu)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734142_58734144delinsCTG , CM000679.2:g.58734142_58734144delinsCTG GRCh38
NC_000017.10:g.56811503_56811505delinsCTG , CM000679.1:g.56811503_56811505delinsCTG GRCh37
NC_000017.9:g.54166502_54166504delinsCTG NCBI36
NG_023199.1:g.46541_46543delinsCTG , LRG_314:g.46541_46543delinsCTG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1051_1053delinsCTG MANE Select NP_478123.1:p.Val351Leu
ENST00000337432.9:c.1051_1053delinsCTG MANE Select ENSP00000336701.4:p.Val351Leu
NM_058216.2:c.1051_1053delinsCTG NP_478123.1:p.Val351Leu
NR_103872.1:n.955_957delinsCTG
NR_103872.2:n.926_928delinsCTG
ENST00000337432.8:c.1051_1053delinsCTG ENSP00000336701.4:p.Val351Leu
ENST00000413590.5:c.692_694delinsCTG
ENST00000461271.6:c.*1583_*1585delinsCTG ENSP00000464056.2:n.*1583_*1585delinsCTG
ENST00000461706.1:n.238_240delinsCTG
ENST00000475762.5:c.*1687_*1689delinsCTG ENSP00000432421.1:n.*1687_*1689delinsCTG
ENST00000482007.5:c.*479_*481delinsCTG ENSP00000433332.1:n.*479_*481delinsCTG
ENST00000487525.5:c.*627_*629delinsCTG ENSP00000431637.1:n.*627_*629delinsCTG
ENST00000578151.1:n.264_266delinsCTG
ENST00000581221.5:n.566_568delinsCTG
ENST00000584804.1:c.285_287delinsCTG ENSP00000463658.1:p.Leu95PhefsTer2
ENST00000697680.1:c.*2015_*2017delinsCTG ENSP00000513392.1:n.*2015_*2017delinsCTG
ENST00000697681.1:c.*2212_*2214delinsCTG ENSP00000513393.1:n.*2212_*2214delinsCTG
ENST00000697683.1:c.*1987_*1989delinsCTG ENSP00000513395.1:n.*1987_*1989delinsCTG
ENST00000697685.1:c.*1748_*1750delinsCTG ENSP00000513396.1:n.*1748_*1750delinsCTG
ENST00000697686.1:c.822_824delinsCTG ENSP00000513397.1:p.Leu274PhefsTer2
ENST00000697689.1:c.*1465_*1467delinsCTG ENSP00000513398.1:n.*1465_*1467delinsCTG
ENST00000697690.1:c.*11_*13delinsCTG ENSP00000513399.1:n.*11_*13delinsCTG
ENST00000697691.1:c.*1023_*1025delinsCTG ENSP00000513400.1:n.*1023_*1025delinsCTG
ENST00000697692.1:c.*1063_*1065delinsCTG ENSP00000513401.1:n.*1063_*1065delinsCTG
ENST00000697694.1:c.700_702delinsCTG ENSP00000513402.1:p.Val234Leu
ENST00000697695.1:n.1658_1660delinsCTG
XM_006722001.2:c.1054_1056delinsCTG XP_006722064.1:p.Val352Leu
XM_006722001.4:c.1054_1056delinsCTG XP_006722064.1:p.Val352Leu
XM_006722002.2:c.990_992delinsCTG XP_006722065.1:p.Leu330PhefsTer2
XM_006722002.4:c.990_992delinsCTG XP_006722065.1:p.Leu330PhefsTer2
XM_006722004.2:c.703_705delinsCTG XP_006722067.1:p.Val235Leu
XM_006722004.3:c.703_705delinsCTG XP_006722067.1:p.Val235Leu
XM_006722005.2:c.703_705delinsCTG XP_006722068.1:p.Val235Leu
XM_006722005.3:c.703_705delinsCTG XP_006722068.1:p.Val235Leu
XM_011525092.1:c.703_705delinsCTG XP_011523394.1:p.Val235Leu
XM_011525092.2:c.703_705delinsCTG XP_011523394.1:p.Val235Leu
XM_011525093.1:c.703_705delinsCTG XP_011523395.1:p.Val235Leu
XM_011525093.2:c.703_705delinsCTG XP_011523395.1:p.Val235Leu
XM_011525094.1:c.703_705delinsCTG XP_011523396.1:p.Val235Leu
XM_011525094.2:c.703_705delinsCTG XP_011523396.1:p.Val235Leu
XM_017024914.1:c.700_702delinsCTG XP_016880403.1:p.Val234Leu
XM_017024915.1:c.700_702delinsCTG XP_016880404.1:p.Val234Leu
XM_017024916.1:c.700_702delinsCTG XP_016880405.1:p.Val234Leu
XM_017024917.1:c.700_702delinsCTG XP_016880406.1:p.Val234Leu
XM_017024918.2:c.700_702delinsCTG XP_016880407.1:p.Val234Leu
XM_017024919.1:c.639_641delinsCTG XP_016880408.1:p.Leu213PhefsTer2
XR_934513.1:n.1269_1271delinsCTG
XR_934513.3:n.1700_1702delinsCTG
XR_934514.1:n.1272_1274delinsCTG
XR_934514.3:n.1703_1705delinsCTG
XR_934886.1:n.149+3927_149+3929delinsCAG
XR_934886.2:n.149+3927_149+3929delinsCAG