Canonical Allele Identifier: CA3261178761
Community Standard Title: NM_058216.3(RAD51C):c.19_21delinsTGT (p.Arg7Cys)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692662_58692664delinsTGT , CM000679.2:g.58692662_58692664delinsTGT GRCh38
NC_000017.10:g.56770023_56770025delinsTGT , CM000679.1:g.56770023_56770025delinsTGT GRCh37
NC_000017.9:g.54125022_54125024delinsTGT NCBI36
NG_023199.1:g.5061_5063delinsTGT , LRG_314:g.5061_5063delinsTGT
NG_047169.1:g.4416_4418delinsACA

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.19_21delinsTGT MANE Select NP_478123.1:p.Arg7Cys
ENST00000337432.9:c.19_21delinsTGT MANE Select ENSP00000336701.4:p.Arg7Cys
NM_002876.3:c.19_21delinsTGT NP_002867.1:p.Arg7Cys
NM_002876.4:c.19_21delinsTGT NP_002867.1:p.Arg7Cys
NM_058216.2:c.19_21delinsTGT NP_478123.1:p.Arg7Cys
NR_103872.1:n.90_92delinsTGT
NR_103872.2:n.61_63delinsTGT
NR_103873.1:n.90_92delinsTGT
ENST00000337432.8:c.19_21delinsTGT ENSP00000336701.4:p.Arg7Cys
ENST00000421782.3:c.19_21delinsTGT ENSP00000391450.2:p.Arg7Cys
ENST00000461271.5:c.-230_-228delinsTGT ENSP00000464056.1:n.-230_-228delinsTGT
ENST00000461271.6:c.-230_-228delinsTGT ENSP00000464056.2:n.-230_-228delinsTGT
ENST00000475762.5:c.19_21delinsTGT ENSP00000432421.1:p.Arg7Cys
ENST00000476741.2:n.61_63delinsTGT
ENST00000482007.5:c.19_21delinsTGT ENSP00000433332.1:p.Arg7Cys
ENST00000486827.1:c.19_21delinsTGT ENSP00000436761.1:p.Arg7Cys
ENST00000487525.5:c.19_21delinsTGT ENSP00000431637.1:p.Arg7Cys
ENST00000487921.5:n.57+30_57+32delinsTGT
ENST00000583539.5:c.19_21delinsTGT ENSP00000463121.1:p.Arg7Cys
ENST00000697675.1:n.90_92delinsTGT
ENST00000697676.1:n.79_81delinsTGT
ENST00000697677.1:n.77_79delinsTGT
ENST00000697678.1:n.47+30_47+32delinsTGT
ENST00000697679.1:n.70_72delinsTGT
ENST00000697680.1:c.19_21delinsTGT ENSP00000513392.1:p.Arg7Cys
ENST00000697681.1:c.19_21delinsTGT ENSP00000513393.1:p.Arg7Cys
ENST00000697683.1:c.19_21delinsTGT ENSP00000513395.1:p.Arg7Cys
ENST00000697684.1:n.79_81delinsTGT
ENST00000697685.1:c.19_21delinsTGT ENSP00000513396.1:p.Arg7Cys
ENST00000697686.1:c.-207+30_-207+32delinsTGT ENSP00000513397.1:n.-207+30_-207+32delinsTGT
ENST00000697687.1:n.65_67delinsTGT
ENST00000697688.1:n.65_67delinsTGT
ENST00000697689.1:c.19_21delinsTGT ENSP00000513398.1:p.Arg7Cys
ENST00000697690.1:c.19_21delinsTGT ENSP00000513399.1:p.Arg7Cys
ENST00000697691.1:c.19_21delinsTGT ENSP00000513400.1:p.Arg7Cys
ENST00000697692.1:c.19_21delinsTGT ENSP00000513401.1:p.Arg7Cys
XM_006722001.2:c.19_21delinsTGT XP_006722064.1:p.Arg7Cys
XM_006722001.4:c.19_21delinsTGT XP_006722064.1:p.Arg7Cys
XM_006722002.2:c.19_21delinsTGT XP_006722065.1:p.Arg7Cys
XM_006722002.4:c.19_21delinsTGT XP_006722065.1:p.Arg7Cys
XM_006722004.2:c.-230_-228delinsTGT XP_006722067.1:n.-230_-228delinsTGT
XM_006722004.3:c.-230_-228delinsTGT XP_006722067.1:n.-230_-228delinsTGT
XM_006722005.2:c.-207+30_-207+32delinsTGT XP_006722068.1:n.-207+30_-207+32delinsTGT
XM_006722005.3:c.-207+30_-207+32delinsTGT XP_006722068.1:n.-207+30_-207+32delinsTGT
XM_011525092.1:c.-530_-528delinsTGT XP_011523394.1:n.-530_-528delinsTGT
XM_011525093.1:c.-691_-689delinsTGT XP_011523395.1:n.-691_-689delinsTGT
XM_017024914.1:c.-230_-228delinsTGT XP_016880403.1:n.-230_-228delinsTGT
XM_017024916.1:c.-530_-528delinsTGT XP_016880405.1:n.-530_-528delinsTGT
XM_017024917.1:c.-207+30_-207+32delinsTGT XP_016880406.1:n.-207+30_-207+32delinsTGT
XM_017024918.2:c.-504_-502delinsTGT XP_016880407.1:n.-504_-502delinsTGT
XR_934513.1:n.92_94delinsTGT
XR_934513.3:n.523_525delinsTGT
XR_934514.1:n.92_94delinsTGT
XR_934514.3:n.523_525delinsTGT