Canonical Allele Identifier: CA3261178822
Community Standard Title: NM_058216.3(RAD51C):c.20_21delinsCT (p.Arg7Pro)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692663_58692664delinsCT , CM000679.2:g.58692663_58692664delinsCT GRCh38
NC_000017.10:g.56770024_56770025delinsCT , CM000679.1:g.56770024_56770025delinsCT GRCh37
NC_000017.9:g.54125023_54125024delinsCT NCBI36
NG_023199.1:g.5062_5063delinsCT , LRG_314:g.5062_5063delinsCT
NG_047169.1:g.4416_4417delinsAG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.20_21delinsCT MANE Select NP_478123.1:p.Arg7Pro
ENST00000337432.9:c.20_21delinsCT MANE Select ENSP00000336701.4:p.Arg7Pro
NM_002876.3:c.20_21delinsCT NP_002867.1:p.Arg7Pro
NM_002876.4:c.20_21delinsCT NP_002867.1:p.Arg7Pro
NM_058216.2:c.20_21delinsCT NP_478123.1:p.Arg7Pro
NR_103872.1:n.91_92delinsCT
NR_103872.2:n.62_63delinsCT
NR_103873.1:n.91_92delinsCT
ENST00000337432.8:c.20_21delinsCT ENSP00000336701.4:p.Arg7Pro
ENST00000421782.3:c.20_21delinsCT ENSP00000391450.2:p.Arg7Pro
ENST00000461271.5:c.-229_-228delinsCT ENSP00000464056.1:n.-229_-228delinsCT
ENST00000461271.6:c.-229_-228delinsCT ENSP00000464056.2:n.-229_-228delinsCT
ENST00000475762.5:c.20_21delinsCT ENSP00000432421.1:p.Arg7Pro
ENST00000476741.2:n.62_63delinsCT
ENST00000482007.5:c.20_21delinsCT ENSP00000433332.1:p.Arg7Pro
ENST00000486827.1:c.20_21delinsCT ENSP00000436761.1:p.Arg7Pro
ENST00000487525.5:c.20_21delinsCT ENSP00000431637.1:p.Arg7Pro
ENST00000487921.5:n.57+31_57+32delinsCT
ENST00000583539.5:c.20_21delinsCT ENSP00000463121.1:p.Arg7Pro
ENST00000584617.5:c.1_2delinsCT
ENST00000697675.1:n.91_92delinsCT
ENST00000697676.1:n.80_81delinsCT
ENST00000697677.1:n.78_79delinsCT
ENST00000697678.1:n.47+31_47+32delinsCT
ENST00000697679.1:n.71_72delinsCT
ENST00000697680.1:c.20_21delinsCT ENSP00000513392.1:p.Arg7Pro
ENST00000697681.1:c.20_21delinsCT ENSP00000513393.1:p.Arg7Pro
ENST00000697683.1:c.20_21delinsCT ENSP00000513395.1:p.Arg7Pro
ENST00000697684.1:n.80_81delinsCT
ENST00000697685.1:c.20_21delinsCT ENSP00000513396.1:p.Arg7Pro
ENST00000697686.1:c.-207+31_-207+32delinsCT ENSP00000513397.1:n.-207+31_-207+32delinsCT
ENST00000697687.1:n.66_67delinsCT
ENST00000697688.1:n.66_67delinsCT
ENST00000697689.1:c.20_21delinsCT ENSP00000513398.1:p.Arg7Pro
ENST00000697690.1:c.20_21delinsCT ENSP00000513399.1:p.Arg7Pro
ENST00000697691.1:c.20_21delinsCT ENSP00000513400.1:p.Arg7Pro
ENST00000697692.1:c.20_21delinsCT ENSP00000513401.1:p.Arg7Pro
XM_006722001.2:c.20_21delinsCT XP_006722064.1:p.Arg7Pro
XM_006722001.4:c.20_21delinsCT XP_006722064.1:p.Arg7Pro
XM_006722002.2:c.20_21delinsCT XP_006722065.1:p.Arg7Pro
XM_006722002.4:c.20_21delinsCT XP_006722065.1:p.Arg7Pro
XM_006722004.2:c.-229_-228delinsCT XP_006722067.1:n.-229_-228delinsCT
XM_006722004.3:c.-229_-228delinsCT XP_006722067.1:n.-229_-228delinsCT
XM_006722005.2:c.-207+31_-207+32delinsCT XP_006722068.1:n.-207+31_-207+32delinsCT
XM_006722005.3:c.-207+31_-207+32delinsCT XP_006722068.1:n.-207+31_-207+32delinsCT
XM_011525092.1:c.-529_-528delinsCT XP_011523394.1:n.-529_-528delinsCT
XM_011525093.1:c.-690_-689delinsCT XP_011523395.1:n.-690_-689delinsCT
XM_017024914.1:c.-229_-228delinsCT XP_016880403.1:n.-229_-228delinsCT
XM_017024916.1:c.-529_-528delinsCT XP_016880405.1:n.-529_-528delinsCT
XM_017024917.1:c.-207+31_-207+32delinsCT XP_016880406.1:n.-207+31_-207+32delinsCT
XM_017024918.2:c.-503_-502delinsCT XP_016880407.1:n.-503_-502delinsCT
XR_934513.1:n.93_94delinsCT
XR_934513.3:n.524_525delinsCT
XR_934514.1:n.93_94delinsCT
XR_934514.3:n.524_525delinsCT