Canonical Allele Identifier: CA3057243156
Community Standard Title: NM_058216.3(RAD51C):c.979_981del (p.Tyr327del)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58732497_58732499del , CM000679.2:g.58732497_58732499del GRCh38
NC_000017.10:g.56809858_56809860del , CM000679.1:g.56809858_56809860del GRCh37
NC_000017.9:g.54164857_54164859del NCBI36
NG_023199.1:g.44896_44898del , LRG_314:g.44896_44898del

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.979_981del MANE Select NP_478123.1:p.Tyr327del
ENST00000337432.9:c.979_981del MANE Select ENSP00000336701.4:p.Tyr327del
NM_058216.2:c.979_981del NP_478123.1:p.Tyr327del
NR_103872.1:n.883_885del
NR_103872.2:n.854_856del
ENST00000337432.8:c.979_981del ENSP00000336701.4:p.Tyr327del
ENST00000413590.5:c.620_622del
ENST00000461271.6:c.628_630del ENSP00000464056.2:p.Tyr210del
ENST00000461706.1:n.166_168del
ENST00000475762.5:c.*1615_*1617del ENSP00000432421.1:n.*1615_*1617del
ENST00000482007.5:c.*407_*409del ENSP00000433332.1:n.*407_*409del
ENST00000487525.5:c.*555_*557del ENSP00000431637.1:n.*555_*557del
ENST00000578151.1:n.240-1621_240-1619del
ENST00000581221.5:n.494_496del
ENST00000583539.5:c.979_981del ENSP00000463121.1:p.Tyr327del
ENST00000584617.5:c.701_703del
ENST00000584804.1:c.213_215del ENSP00000463658.1:p.Cys71Ter
ENST00000697680.1:c.*1943_*1945del ENSP00000513392.1:n.*1943_*1945del
ENST00000697681.1:c.*2140_*2142del ENSP00000513393.1:n.*2140_*2142del
ENST00000697683.1:c.*1915_*1917del ENSP00000513395.1:n.*1915_*1917del
ENST00000697685.1:c.*1676_*1678del ENSP00000513396.1:n.*1676_*1678del
ENST00000697686.1:c.750_752del ENSP00000513397.1:p.Cys250Ter
ENST00000697689.1:c.*1441-1621_*1441-1619del ENSP00000513398.1:n.*1441-1621_*1441-1619del
ENST00000697690.1:c.905-1621_905-1619del ENSP00000513399.1:n.905-1621_905-1619del
ENST00000697691.1:c.*951_*953del ENSP00000513400.1:n.*951_*953del
ENST00000697692.1:c.*991_*993del ENSP00000513401.1:n.*991_*993del
ENST00000697694.1:c.628_630del ENSP00000513402.1:p.Tyr210del
ENST00000697695.1:n.1586_1588del
XM_006722001.2:c.982_984del XP_006722064.1:p.Tyr328del
XM_006722001.4:c.982_984del XP_006722064.1:p.Tyr328del
XM_006722002.2:c.918_920del XP_006722065.1:p.Cys306Ter
XM_006722002.4:c.918_920del XP_006722065.1:p.Cys306Ter
XM_006722004.2:c.631_633del XP_006722067.1:p.Tyr211del
XM_006722004.3:c.631_633del XP_006722067.1:p.Tyr211del
XM_006722005.2:c.631_633del XP_006722068.1:p.Tyr211del
XM_006722005.3:c.631_633del XP_006722068.1:p.Tyr211del
XM_011525092.1:c.631_633del XP_011523394.1:p.Tyr211del
XM_011525092.2:c.631_633del XP_011523394.1:p.Tyr211del
XM_011525093.1:c.631_633del XP_011523395.1:p.Tyr211del
XM_011525093.2:c.631_633del XP_011523395.1:p.Tyr211del
XM_011525094.1:c.631_633del XP_011523396.1:p.Tyr211del
XM_011525094.2:c.631_633del XP_011523396.1:p.Tyr211del
XM_017024914.1:c.628_630del XP_016880403.1:p.Tyr210del
XM_017024915.1:c.628_630del XP_016880404.1:p.Tyr210del
XM_017024916.1:c.628_630del XP_016880405.1:p.Tyr210del
XM_017024917.1:c.628_630del XP_016880406.1:p.Tyr210del
XM_017024918.2:c.628_630del XP_016880407.1:p.Tyr210del
XM_017024919.1:c.567_569del XP_016880408.1:p.Cys189Ter
XR_934513.1:n.1197_1199del
XR_934513.3:n.1628_1630del
XR_934514.1:n.1200_1202del
XR_934514.3:n.1631_1633del
XR_934886.1:n.149+5572_149+5574del
XR_934886.2:n.149+5572_149+5574del