Canonical Allele Identifier: CA3261179395
Community Standard Title: NM_058216.3(RAD51C):c.59_60delinsGC (p.Ser20Cys)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692702_58692703delinsGC , CM000679.2:g.58692702_58692703delinsGC GRCh38
NC_000017.10:g.56770063_56770064delinsGC , CM000679.1:g.56770063_56770064delinsGC GRCh37
NC_000017.9:g.54125062_54125063delinsGC NCBI36
NG_023199.1:g.5101_5102delinsGC , LRG_314:g.5101_5102delinsGC
NG_047169.1:g.4377_4378delinsGC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.59_60delinsGC MANE Select NP_478123.1:p.Ser20Cys
ENST00000337432.9:c.59_60delinsGC MANE Select ENSP00000336701.4:p.Ser20Cys
NM_002876.3:c.59_60delinsGC NP_002867.1:p.Ser20Cys
NM_002876.4:c.59_60delinsGC NP_002867.1:p.Ser20Cys
NM_058216.2:c.59_60delinsGC NP_478123.1:p.Ser20Cys
NR_103872.1:n.130_131delinsGC
NR_103872.2:n.101_102delinsGC
NR_103873.1:n.113+17_113+18delinsGC
ENST00000337432.8:c.59_60delinsGC ENSP00000336701.4:p.Ser20Cys
ENST00000421782.3:c.59_60delinsGC ENSP00000391450.2:p.Ser20Cys
ENST00000461271.5:c.-207+17_-207+18delinsGC ENSP00000464056.1:n.-207+17_-207+18delinsGC
ENST00000461271.6:c.-207+17_-207+18delinsGC ENSP00000464056.2:n.-207+17_-207+18delinsGC
ENST00000475762.5:c.59_60delinsGC ENSP00000432421.1:p.Ser20Cys
ENST00000476741.2:n.101_102delinsGC
ENST00000482007.5:c.59_60delinsGC ENSP00000433332.1:p.Ser20Cys
ENST00000486827.1:c.59_60delinsGC ENSP00000436761.1:p.Ser20Cys
ENST00000487525.5:c.59_60delinsGC ENSP00000431637.1:p.Ser20Cys
ENST00000487921.5:n.57+70_57+71delinsGC
ENST00000583539.5:c.59_60delinsGC ENSP00000463121.1:p.Ser20Cys
ENST00000584617.5:c.40_41delinsGC
ENST00000697675.1:n.130_131delinsGC
ENST00000697676.1:n.119_120delinsGC
ENST00000697677.1:n.117_118delinsGC
ENST00000697678.1:n.47+70_47+71delinsGC
ENST00000697679.1:n.110_111delinsGC
ENST00000697680.1:c.59_60delinsGC ENSP00000513392.1:p.Ser20Cys
ENST00000697681.1:c.59_60delinsGC ENSP00000513393.1:p.Ser20Cys
ENST00000697683.1:c.59_60delinsGC ENSP00000513395.1:p.Ser20Cys
ENST00000697684.1:n.119_120delinsGC
ENST00000697685.1:c.59_60delinsGC ENSP00000513396.1:p.Ser20Cys
ENST00000697686.1:c.-207+70_-207+71delinsGC ENSP00000513397.1:n.-207+70_-207+71delinsGC
ENST00000697687.1:n.105_106delinsGC
ENST00000697688.1:n.105_106delinsGC
ENST00000697689.1:c.59_60delinsGC ENSP00000513398.1:p.Ser20Cys
ENST00000697690.1:c.59_60delinsGC ENSP00000513399.1:p.Ser20Cys
ENST00000697691.1:c.42+17_42+18delinsGC ENSP00000513400.1:n.42+17_42+18delinsGC
ENST00000697692.1:c.59_60delinsGC ENSP00000513401.1:p.Ser20Cys
XM_006722001.2:c.59_60delinsGC XP_006722064.1:p.Ser20Cys
XM_006722001.4:c.59_60delinsGC XP_006722064.1:p.Ser20Cys
XM_006722002.2:c.59_60delinsGC XP_006722065.1:p.Ser20Cys
XM_006722002.4:c.59_60delinsGC XP_006722065.1:p.Ser20Cys
XM_006722004.2:c.-207+17_-207+18delinsGC XP_006722067.1:n.-207+17_-207+18delinsGC
XM_006722004.3:c.-207+17_-207+18delinsGC XP_006722067.1:n.-207+17_-207+18delinsGC
XM_006722005.2:c.-207+70_-207+71delinsGC XP_006722068.1:n.-207+70_-207+71delinsGC
XM_006722005.3:c.-207+70_-207+71delinsGC XP_006722068.1:n.-207+70_-207+71delinsGC
XM_011525092.1:c.-507+17_-507+18delinsGC XP_011523394.1:n.-507+17_-507+18delinsGC
XM_011525092.2:c.-507+17_-507+18delinsGC XP_011523394.1:n.-507+17_-507+18delinsGC
XM_011525093.1:c.-668+17_-668+18delinsGC XP_011523395.1:n.-668+17_-668+18delinsGC
XM_011525093.2:c.-668+17_-668+18delinsGC XP_011523395.1:n.-668+17_-668+18delinsGC
XM_017024914.1:c.-207+17_-207+18delinsGC XP_016880403.1:n.-207+17_-207+18delinsGC
XM_017024916.1:c.-507+17_-507+18delinsGC XP_016880405.1:n.-507+17_-507+18delinsGC
XM_017024917.1:c.-207+70_-207+71delinsGC XP_016880406.1:n.-207+70_-207+71delinsGC
XM_017024918.2:c.-464_-463delinsGC XP_016880407.1:n.-464_-463delinsGC
XM_017024919.1:c.-668+17_-668+18delinsGC XP_016880408.1:n.-668+17_-668+18delinsGC
XR_934513.1:n.132_133delinsGC
XR_934513.3:n.563_564delinsGC
XR_934514.1:n.132_133delinsGC
XR_934514.3:n.563_564delinsGC