Canonical Allele Identifier: CA3261179724
Community Standard Title: NM_058216.3(RAD51C):c.82_84delinsCTC (p.Val28Leu)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692725_58692727delinsCTC , CM000679.2:g.58692725_58692727delinsCTC GRCh38
NC_000017.10:g.56770086_56770088delinsCTC , CM000679.1:g.56770086_56770088delinsCTC GRCh37
NC_000017.9:g.54125085_54125087delinsCTC NCBI36
NG_023199.1:g.5124_5126delinsCTC , LRG_314:g.5124_5126delinsCTC
NG_047169.1:g.4353_4355delinsGAG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.82_84delinsCTC MANE Select NP_478123.1:p.Val28Leu
ENST00000337432.9:c.82_84delinsCTC MANE Select ENSP00000336701.4:p.Val28Leu
NM_002876.3:c.82_84delinsCTC NP_002867.1:p.Val28Leu
NM_002876.4:c.82_84delinsCTC NP_002867.1:p.Val28Leu
NM_058216.2:c.82_84delinsCTC NP_478123.1:p.Val28Leu
NR_103872.1:n.153_155delinsCTC
NR_103872.2:n.124_126delinsCTC
NR_103873.1:n.113+40_113+42delinsCTC
ENST00000337432.8:c.82_84delinsCTC ENSP00000336701.4:p.Val28Leu
ENST00000421782.3:c.82_84delinsCTC ENSP00000391450.2:p.Val28Leu
ENST00000461271.5:c.-207+40_-207+42delinsCTC ENSP00000464056.1:n.-207+40_-207+42delinsCTC
ENST00000461271.6:c.-207+40_-207+42delinsCTC ENSP00000464056.2:n.-207+40_-207+42delinsCTC
ENST00000475762.5:c.82_84delinsCTC ENSP00000432421.1:p.Val28Leu
ENST00000476741.2:n.124_126delinsCTC
ENST00000482007.5:c.82_84delinsCTC ENSP00000433332.1:p.Val28Leu
ENST00000486827.1:c.82_84delinsCTC ENSP00000436761.1:p.Val28Leu
ENST00000487525.5:c.82_84delinsCTC ENSP00000431637.1:p.Val28Leu
ENST00000487921.5:n.57+93_57+95delinsCTC
ENST00000583539.5:c.82_84delinsCTC ENSP00000463121.1:p.Val28Leu
ENST00000584617.5:c.63_65delinsCTC
ENST00000697675.1:n.153_155delinsCTC
ENST00000697676.1:n.142_144delinsCTC
ENST00000697677.1:n.140_142delinsCTC
ENST00000697678.1:n.47+93_47+95delinsCTC
ENST00000697679.1:n.133_135delinsCTC
ENST00000697680.1:c.82_84delinsCTC ENSP00000513392.1:p.Val28Leu
ENST00000697681.1:c.82_84delinsCTC ENSP00000513393.1:p.Val28Leu
ENST00000697683.1:c.82_84delinsCTC ENSP00000513395.1:p.Val28Leu
ENST00000697684.1:n.142_144delinsCTC
ENST00000697685.1:c.82_84delinsCTC ENSP00000513396.1:p.Val28Leu
ENST00000697686.1:c.-207+93_-207+95delinsCTC ENSP00000513397.1:n.-207+93_-207+95delinsCTC
ENST00000697687.1:n.128_130delinsCTC
ENST00000697688.1:n.128_130delinsCTC
ENST00000697689.1:c.82_84delinsCTC ENSP00000513398.1:p.Val28Leu
ENST00000697690.1:c.82_84delinsCTC ENSP00000513399.1:p.Val28Leu
ENST00000697691.1:c.42+40_42+42delinsCTC ENSP00000513400.1:n.42+40_42+42delinsCTC
ENST00000697692.1:c.82_84delinsCTC ENSP00000513401.1:p.Val28Leu
XM_006722001.2:c.82_84delinsCTC XP_006722064.1:p.Val28Leu
XM_006722001.4:c.82_84delinsCTC XP_006722064.1:p.Val28Leu
XM_006722002.2:c.82_84delinsCTC XP_006722065.1:p.Val28Leu
XM_006722002.4:c.82_84delinsCTC XP_006722065.1:p.Val28Leu
XM_006722004.2:c.-207+40_-207+42delinsCTC XP_006722067.1:n.-207+40_-207+42delinsCTC
XM_006722004.3:c.-207+40_-207+42delinsCTC XP_006722067.1:n.-207+40_-207+42delinsCTC
XM_006722005.2:c.-207+93_-207+95delinsCTC XP_006722068.1:n.-207+93_-207+95delinsCTC
XM_006722005.3:c.-207+93_-207+95delinsCTC XP_006722068.1:n.-207+93_-207+95delinsCTC
XM_011525092.1:c.-507+40_-507+42delinsCTC XP_011523394.1:n.-507+40_-507+42delinsCTC
XM_011525092.2:c.-507+40_-507+42delinsCTC XP_011523394.1:n.-507+40_-507+42delinsCTC
XM_011525093.1:c.-668+40_-668+42delinsCTC XP_011523395.1:n.-668+40_-668+42delinsCTC
XM_011525093.2:c.-668+40_-668+42delinsCTC XP_011523395.1:n.-668+40_-668+42delinsCTC
XM_017024914.1:c.-207+40_-207+42delinsCTC XP_016880403.1:n.-207+40_-207+42delinsCTC
XM_017024916.1:c.-507+40_-507+42delinsCTC XP_016880405.1:n.-507+40_-507+42delinsCTC
XM_017024917.1:c.-207+93_-207+95delinsCTC XP_016880406.1:n.-207+93_-207+95delinsCTC
XM_017024918.2:c.-441_-439delinsCTC XP_016880407.1:n.-441_-439delinsCTC
XM_017024919.1:c.-668+40_-668+42delinsCTC XP_016880408.1:n.-668+40_-668+42delinsCTC
XR_934513.1:n.155_157delinsCTC
XR_934513.3:n.586_588delinsCTC
XR_934514.1:n.155_157delinsCTC
XR_934514.3:n.586_588delinsCTC