Canonical Allele Identifier: CA3261180501
Community Standard Title: NM_058216.3(RAD51C):c.826_828delinsTAT (p.His276Tyr)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709979_58709981delinsTAT , CM000679.2:g.58709979_58709981delinsTAT GRCh38
NC_000017.10:g.56787340_56787342delinsTAT , CM000679.1:g.56787340_56787342delinsTAT GRCh37
NC_000017.9:g.54142339_54142341delinsTAT NCBI36
NG_023199.1:g.22378_22380delinsTAT , LRG_314:g.22378_22380delinsTAT

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.826_828delinsTAT MANE Select NP_478123.1:p.His276Tyr
ENST00000337432.9:c.826_828delinsTAT MANE Select ENSP00000336701.4:p.His276Tyr
NM_058216.2:c.826_828delinsTAT NP_478123.1:p.His276Tyr
NR_103872.1:n.730_732delinsTAT
NR_103872.2:n.701_703delinsTAT
ENST00000337432.8:c.826_828delinsTAT ENSP00000336701.4:p.His276Tyr
ENST00000413590.5:c.464_466delinsTAT
ENST00000461271.6:c.475_477delinsTAT ENSP00000464056.2:p.His159Tyr
ENST00000475762.5:c.*1529_*1531delinsTAT ENSP00000432421.1:n.*1529_*1531delinsTAT
ENST00000482007.5:c.*254_*256delinsTAT ENSP00000433332.1:n.*254_*256delinsTAT
ENST00000487525.5:c.*399_*401delinsTAT ENSP00000431637.1:n.*399_*401delinsTAT
ENST00000578151.1:n.161_163delinsTAT
ENST00000581221.5:n.341_343delinsTAT
ENST00000583539.5:c.826_828delinsTAT ENSP00000463121.1:p.His276Tyr
ENST00000584617.5:c.548_550delinsTAT
ENST00000584804.1:c.121_123delinsTAT ENSP00000463658.1:p.His41Tyr
ENST00000697678.1:n.728_730delinsTAT
ENST00000697679.1:n.1900_1902delinsTAT
ENST00000697680.1:c.*1690_*1692delinsTAT ENSP00000513392.1:n.*1690_*1692delinsTAT
ENST00000697681.1:c.*1987_*1989delinsTAT ENSP00000513393.1:n.*1987_*1989delinsTAT
ENST00000697683.1:c.*1690_*1692delinsTAT ENSP00000513395.1:n.*1690_*1692delinsTAT
ENST00000697684.1:n.886_888delinsTAT
ENST00000697685.1:c.*1523_*1525delinsTAT ENSP00000513396.1:n.*1523_*1525delinsTAT
ENST00000697686.1:c.475_477delinsTAT ENSP00000513397.1:p.His159Tyr
ENST00000697687.1:n.705_707delinsTAT
ENST00000697688.1:n.872_874delinsTAT
ENST00000697689.1:c.*1362_*1364delinsTAT ENSP00000513398.1:n.*1362_*1364delinsTAT
ENST00000697690.1:c.826_828delinsTAT ENSP00000513399.1:p.His276Tyr
ENST00000697691.1:c.*798_*800delinsTAT ENSP00000513400.1:n.*798_*800delinsTAT
ENST00000697692.1:c.*838_*840delinsTAT ENSP00000513401.1:n.*838_*840delinsTAT
ENST00000697694.1:c.475_477delinsTAT ENSP00000513402.1:p.His159Tyr
ENST00000697695.1:n.1433_1435delinsTAT
XM_006722001.2:c.826_828delinsTAT XP_006722064.1:p.His276Tyr
XM_006722001.4:c.826_828delinsTAT XP_006722064.1:p.His276Tyr
XM_006722002.2:c.826_828delinsTAT XP_006722065.1:p.His276Tyr
XM_006722002.4:c.826_828delinsTAT XP_006722065.1:p.His276Tyr
XM_006722004.2:c.475_477delinsTAT XP_006722067.1:p.His159Tyr
XM_006722004.3:c.475_477delinsTAT XP_006722067.1:p.His159Tyr
XM_006722005.2:c.475_477delinsTAT XP_006722068.1:p.His159Tyr
XM_006722005.3:c.475_477delinsTAT XP_006722068.1:p.His159Tyr
XM_011525092.1:c.475_477delinsTAT XP_011523394.1:p.His159Tyr
XM_011525092.2:c.475_477delinsTAT XP_011523394.1:p.His159Tyr
XM_011525093.1:c.475_477delinsTAT XP_011523395.1:p.His159Tyr
XM_011525093.2:c.475_477delinsTAT XP_011523395.1:p.His159Tyr
XM_011525094.1:c.475_477delinsTAT XP_011523396.1:p.His159Tyr
XM_011525094.2:c.475_477delinsTAT XP_011523396.1:p.His159Tyr
XM_017024914.1:c.475_477delinsTAT XP_016880403.1:p.His159Tyr
XM_017024915.1:c.475_477delinsTAT XP_016880404.1:p.His159Tyr
XM_017024916.1:c.475_477delinsTAT XP_016880405.1:p.His159Tyr
XM_017024917.1:c.475_477delinsTAT XP_016880406.1:p.His159Tyr
XM_017024918.2:c.475_477delinsTAT XP_016880407.1:p.His159Tyr
XM_017024919.1:c.475_477delinsTAT XP_016880408.1:p.His159Tyr
XR_934513.1:n.1044_1046delinsTAT
XR_934513.3:n.1475_1477delinsTAT
XR_934514.1:n.1044_1046delinsTAT
XR_934514.3:n.1475_1477delinsTAT