Canonical Allele Identifier: CA3261180499
Community Standard Title: NM_058216.3(RAD51C):c.826_828delinsAAT (p.His276Asn)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709979_58709981delinsAAT , CM000679.2:g.58709979_58709981delinsAAT GRCh38
NC_000017.10:g.56787340_56787342delinsAAT , CM000679.1:g.56787340_56787342delinsAAT GRCh37
NC_000017.9:g.54142339_54142341delinsAAT NCBI36
NG_023199.1:g.22378_22380delinsAAT , LRG_314:g.22378_22380delinsAAT

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.826_828delinsAAT MANE Select NP_478123.1:p.His276Asn
ENST00000337432.9:c.826_828delinsAAT MANE Select ENSP00000336701.4:p.His276Asn
NM_058216.2:c.826_828delinsAAT NP_478123.1:p.His276Asn
NR_103872.1:n.730_732delinsAAT
NR_103872.2:n.701_703delinsAAT
ENST00000337432.8:c.826_828delinsAAT ENSP00000336701.4:p.His276Asn
ENST00000413590.5:c.464_466delinsAAT
ENST00000461271.6:c.475_477delinsAAT ENSP00000464056.2:p.His159Asn
ENST00000475762.5:c.*1529_*1531delinsAAT ENSP00000432421.1:n.*1529_*1531delinsAAT
ENST00000482007.5:c.*254_*256delinsAAT ENSP00000433332.1:n.*254_*256delinsAAT
ENST00000487525.5:c.*399_*401delinsAAT ENSP00000431637.1:n.*399_*401delinsAAT
ENST00000578151.1:n.161_163delinsAAT
ENST00000581221.5:n.341_343delinsAAT
ENST00000583539.5:c.826_828delinsAAT ENSP00000463121.1:p.His276Asn
ENST00000584617.5:c.548_550delinsAAT
ENST00000584804.1:c.121_123delinsAAT ENSP00000463658.1:p.His41Asn
ENST00000697678.1:n.728_730delinsAAT
ENST00000697679.1:n.1900_1902delinsAAT
ENST00000697680.1:c.*1690_*1692delinsAAT ENSP00000513392.1:n.*1690_*1692delinsAAT
ENST00000697681.1:c.*1987_*1989delinsAAT ENSP00000513393.1:n.*1987_*1989delinsAAT
ENST00000697683.1:c.*1690_*1692delinsAAT ENSP00000513395.1:n.*1690_*1692delinsAAT
ENST00000697684.1:n.886_888delinsAAT
ENST00000697685.1:c.*1523_*1525delinsAAT ENSP00000513396.1:n.*1523_*1525delinsAAT
ENST00000697686.1:c.475_477delinsAAT ENSP00000513397.1:p.His159Asn
ENST00000697687.1:n.705_707delinsAAT
ENST00000697688.1:n.872_874delinsAAT
ENST00000697689.1:c.*1362_*1364delinsAAT ENSP00000513398.1:n.*1362_*1364delinsAAT
ENST00000697690.1:c.826_828delinsAAT ENSP00000513399.1:p.His276Asn
ENST00000697691.1:c.*798_*800delinsAAT ENSP00000513400.1:n.*798_*800delinsAAT
ENST00000697692.1:c.*838_*840delinsAAT ENSP00000513401.1:n.*838_*840delinsAAT
ENST00000697694.1:c.475_477delinsAAT ENSP00000513402.1:p.His159Asn
ENST00000697695.1:n.1433_1435delinsAAT
XM_006722001.2:c.826_828delinsAAT XP_006722064.1:p.His276Asn
XM_006722001.4:c.826_828delinsAAT XP_006722064.1:p.His276Asn
XM_006722002.2:c.826_828delinsAAT XP_006722065.1:p.His276Asn
XM_006722002.4:c.826_828delinsAAT XP_006722065.1:p.His276Asn
XM_006722004.2:c.475_477delinsAAT XP_006722067.1:p.His159Asn
XM_006722004.3:c.475_477delinsAAT XP_006722067.1:p.His159Asn
XM_006722005.2:c.475_477delinsAAT XP_006722068.1:p.His159Asn
XM_006722005.3:c.475_477delinsAAT XP_006722068.1:p.His159Asn
XM_011525092.1:c.475_477delinsAAT XP_011523394.1:p.His159Asn
XM_011525092.2:c.475_477delinsAAT XP_011523394.1:p.His159Asn
XM_011525093.1:c.475_477delinsAAT XP_011523395.1:p.His159Asn
XM_011525093.2:c.475_477delinsAAT XP_011523395.1:p.His159Asn
XM_011525094.1:c.475_477delinsAAT XP_011523396.1:p.His159Asn
XM_011525094.2:c.475_477delinsAAT XP_011523396.1:p.His159Asn
XM_017024914.1:c.475_477delinsAAT XP_016880403.1:p.His159Asn
XM_017024915.1:c.475_477delinsAAT XP_016880404.1:p.His159Asn
XM_017024916.1:c.475_477delinsAAT XP_016880405.1:p.His159Asn
XM_017024917.1:c.475_477delinsAAT XP_016880406.1:p.His159Asn
XM_017024918.2:c.475_477delinsAAT XP_016880407.1:p.His159Asn
XM_017024919.1:c.475_477delinsAAT XP_016880408.1:p.His159Asn
XR_934513.1:n.1044_1046delinsAAT
XR_934513.3:n.1475_1477delinsAAT
XR_934514.1:n.1044_1046delinsAAT
XR_934514.3:n.1475_1477delinsAAT