Canonical Allele Identifier: CA3261179102
Community Standard Title: NM_058216.3(RAD51C):c.1004_1005delinsAT (p.Cys335Tyr)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58732522_58732523delinsAT , CM000679.2:g.58732522_58732523delinsAT GRCh38
NC_000017.10:g.56809883_56809884delinsAT , CM000679.1:g.56809883_56809884delinsAT GRCh37
NC_000017.9:g.54164882_54164883delinsAT NCBI36
NG_023199.1:g.44921_44922delinsAT , LRG_314:g.44921_44922delinsAT

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1004_1005delinsAT MANE Select NP_478123.1:p.Cys335Tyr
ENST00000337432.9:c.1004_1005delinsAT MANE Select ENSP00000336701.4:p.Cys335Tyr
NM_058216.2:c.1004_1005delinsAT NP_478123.1:p.Cys335Tyr
NR_103872.1:n.908_909delinsAT
NR_103872.2:n.879_880delinsAT
ENST00000337432.8:c.1004_1005delinsAT ENSP00000336701.4:p.Cys335Tyr
ENST00000413590.5:c.645_646delinsAT
ENST00000461271.6:c.653_654delinsAT ENSP00000464056.2:p.Cys218Tyr
ENST00000461706.1:n.191_192delinsAT
ENST00000475762.5:c.*1640_*1641delinsAT ENSP00000432421.1:n.*1640_*1641delinsAT
ENST00000482007.5:c.*432_*433delinsAT ENSP00000433332.1:n.*432_*433delinsAT
ENST00000487525.5:c.*580_*581delinsAT ENSP00000431637.1:n.*580_*581delinsAT
ENST00000578151.1:n.240-1596_240-1595delinsAT
ENST00000581221.5:n.519_520delinsAT
ENST00000583539.5:c.1004_1005delinsAT ENSP00000463121.1:p.Cys335Tyr
ENST00000584804.1:c.238_239delinsAT ENSP00000463658.1:p.Ala80Ile
ENST00000697680.1:c.*1968_*1969delinsAT ENSP00000513392.1:n.*1968_*1969delinsAT
ENST00000697681.1:c.*2165_*2166delinsAT ENSP00000513393.1:n.*2165_*2166delinsAT
ENST00000697683.1:c.*1940_*1941delinsAT ENSP00000513395.1:n.*1940_*1941delinsAT
ENST00000697685.1:c.*1701_*1702delinsAT ENSP00000513396.1:n.*1701_*1702delinsAT
ENST00000697686.1:c.775_776delinsAT ENSP00000513397.1:p.Ala259Ile
ENST00000697689.1:c.*1441-1596_*1441-1595delinsAT ENSP00000513398.1:n.*1441-1596_*1441-1595delinsAT
ENST00000697690.1:c.905-1596_905-1595delinsAT ENSP00000513399.1:n.905-1596_905-1595delinsAT
ENST00000697691.1:c.*976_*977delinsAT ENSP00000513400.1:n.*976_*977delinsAT
ENST00000697692.1:c.*1016_*1017delinsAT ENSP00000513401.1:n.*1016_*1017delinsAT
ENST00000697694.1:c.653_654delinsAT ENSP00000513402.1:p.Cys218Tyr
ENST00000697695.1:n.1611_1612delinsAT
XM_006722001.2:c.1007_1008delinsAT XP_006722064.1:p.Cys336Tyr
XM_006722001.4:c.1007_1008delinsAT XP_006722064.1:p.Cys336Tyr
XM_006722002.2:c.943_944delinsAT XP_006722065.1:p.Ala315Ile
XM_006722002.4:c.943_944delinsAT XP_006722065.1:p.Ala315Ile
XM_006722004.2:c.656_657delinsAT XP_006722067.1:p.Cys219Tyr
XM_006722004.3:c.656_657delinsAT XP_006722067.1:p.Cys219Tyr
XM_006722005.2:c.656_657delinsAT XP_006722068.1:p.Cys219Tyr
XM_006722005.3:c.656_657delinsAT XP_006722068.1:p.Cys219Tyr
XM_011525092.1:c.656_657delinsAT XP_011523394.1:p.Cys219Tyr
XM_011525092.2:c.656_657delinsAT XP_011523394.1:p.Cys219Tyr
XM_011525093.1:c.656_657delinsAT XP_011523395.1:p.Cys219Tyr
XM_011525093.2:c.656_657delinsAT XP_011523395.1:p.Cys219Tyr
XM_011525094.1:c.656_657delinsAT XP_011523396.1:p.Cys219Tyr
XM_011525094.2:c.656_657delinsAT XP_011523396.1:p.Cys219Tyr
XM_017024914.1:c.653_654delinsAT XP_016880403.1:p.Cys218Tyr
XM_017024915.1:c.653_654delinsAT XP_016880404.1:p.Cys218Tyr
XM_017024916.1:c.653_654delinsAT XP_016880405.1:p.Cys218Tyr
XM_017024917.1:c.653_654delinsAT XP_016880406.1:p.Cys218Tyr
XM_017024918.2:c.653_654delinsAT XP_016880407.1:p.Cys218Tyr
XM_017024919.1:c.592_593delinsAT XP_016880408.1:p.Ala198Ile
XR_934513.1:n.1222_1223delinsAT
XR_934513.3:n.1653_1654delinsAT
XR_934514.1:n.1225_1226delinsAT
XR_934514.3:n.1656_1657delinsAT
XR_934886.1:n.149+5548_149+5549delinsAT
XR_934886.2:n.149+5548_149+5549delinsAT