Canonical Allele Identifier: CA3057243379
Community Standard Title: NM_058216.3(RAD51C):c.1059_1061del (p.Ala354del)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734150_58734152del , CM000679.2:g.58734150_58734152del GRCh38
NC_000017.10:g.56811511_56811513del , CM000679.1:g.56811511_56811513del GRCh37
NC_000017.9:g.54166510_54166512del NCBI36
NG_023199.1:g.46549_46551del , LRG_314:g.46549_46551del

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1059_1061del MANE Select NP_478123.1:p.Ala354del
ENST00000337432.9:c.1059_1061del MANE Select ENSP00000336701.4:p.Ala354del
NM_058216.2:c.1059_1061del NP_478123.1:p.Ala354del
NR_103872.1:n.963_965del
NR_103872.2:n.934_936del
ENST00000337432.8:c.1059_1061del ENSP00000336701.4:p.Ala354del
ENST00000413590.5:c.700_702del
ENST00000461271.6:c.*1591_*1593del ENSP00000464056.2:n.*1591_*1593del
ENST00000461706.1:n.246_248del
ENST00000475762.5:c.*1695_*1697del ENSP00000432421.1:n.*1695_*1697del
ENST00000482007.5:c.*487_*489del ENSP00000433332.1:n.*487_*489del
ENST00000487525.5:c.*635_*637del ENSP00000431637.1:n.*635_*637del
ENST00000578151.1:n.272_274del
ENST00000581221.5:n.574_576del
ENST00000584804.1:c.293_295del ENSP00000463658.1:p.Leu98del
ENST00000697680.1:c.*2023_*2025del ENSP00000513392.1:n.*2023_*2025del
ENST00000697681.1:c.*2220_*2222del ENSP00000513393.1:n.*2220_*2222del
ENST00000697683.1:c.*1995_*1997del ENSP00000513395.1:n.*1995_*1997del
ENST00000697685.1:c.*1756_*1758del ENSP00000513396.1:n.*1756_*1758del
ENST00000697686.1:c.830_832del ENSP00000513397.1:p.Leu277del
ENST00000697689.1:c.*1473_*1475del ENSP00000513398.1:n.*1473_*1475del
ENST00000697690.1:c.*19_*21del ENSP00000513399.1:n.*19_*21del
ENST00000697691.1:c.*1031_*1033del ENSP00000513400.1:n.*1031_*1033del
ENST00000697692.1:c.*1071_*1073del ENSP00000513401.1:n.*1071_*1073del
ENST00000697694.1:c.708_710del ENSP00000513402.1:p.Ala237del
ENST00000697695.1:n.1666_1668del
XM_006722001.2:c.1062_1064del XP_006722064.1:p.Ala355del
XM_006722001.4:c.1062_1064del XP_006722064.1:p.Ala355del
XM_006722002.2:c.998_1000del XP_006722065.1:p.Leu333del
XM_006722002.4:c.998_1000del XP_006722065.1:p.Leu333del
XM_006722004.2:c.711_713del XP_006722067.1:p.Ala238del
XM_006722004.3:c.711_713del XP_006722067.1:p.Ala238del
XM_006722005.2:c.711_713del XP_006722068.1:p.Ala238del
XM_006722005.3:c.711_713del XP_006722068.1:p.Ala238del
XM_011525092.1:c.711_713del XP_011523394.1:p.Ala238del
XM_011525092.2:c.711_713del XP_011523394.1:p.Ala238del
XM_011525093.1:c.711_713del XP_011523395.1:p.Ala238del
XM_011525093.2:c.711_713del XP_011523395.1:p.Ala238del
XM_011525094.1:c.711_713del XP_011523396.1:p.Ala238del
XM_011525094.2:c.711_713del XP_011523396.1:p.Ala238del
XM_017024914.1:c.708_710del XP_016880403.1:p.Ala237del
XM_017024915.1:c.708_710del XP_016880404.1:p.Ala237del
XM_017024916.1:c.708_710del XP_016880405.1:p.Ala237del
XM_017024917.1:c.708_710del XP_016880406.1:p.Ala237del
XM_017024918.2:c.708_710del XP_016880407.1:p.Ala237del
XM_017024919.1:c.647_649del XP_016880408.1:p.Leu216del
XR_934513.1:n.1277_1279del
XR_934513.3:n.1708_1710del
XR_934514.1:n.1280_1282del
XR_934514.3:n.1711_1713del
XR_934886.1:n.149+3920_149+3922del
XR_934886.2:n.149+3920_149+3922del