Canonical Allele Identifier: CA3261179364
Community Standard Title: NM_058216.3(RAD51C):c.752_753delinsGA (p.Asp251Gly)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709905_58709906delinsGA , CM000679.2:g.58709905_58709906delinsGA GRCh38
NC_000017.10:g.56787266_56787267delinsGA , CM000679.1:g.56787266_56787267delinsGA GRCh37
NC_000017.9:g.54142265_54142266delinsGA NCBI36
NG_023199.1:g.22304_22305delinsGA , LRG_314:g.22304_22305delinsGA

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.752_753delinsGA MANE Select NP_478123.1:p.Asp251Gly
ENST00000337432.9:c.752_753delinsGA MANE Select ENSP00000336701.4:p.Asp251Gly
NM_058216.2:c.752_753delinsGA NP_478123.1:p.Asp251Gly
NR_103872.1:n.656_657delinsGA
NR_103872.2:n.627_628delinsGA
ENST00000337432.8:c.752_753delinsGA ENSP00000336701.4:p.Asp251Gly
ENST00000413590.5:c.390_391delinsGA
ENST00000461271.5:c.401_402delinsGA ENSP00000464056.1:p.Asp134Gly
ENST00000461271.6:c.401_402delinsGA ENSP00000464056.2:p.Asp134Gly
ENST00000475762.5:c.*1455_*1456delinsGA ENSP00000432421.1:n.*1455_*1456delinsGA
ENST00000482007.5:c.*180_*181delinsGA ENSP00000433332.1:n.*180_*181delinsGA
ENST00000487525.5:c.*325_*326delinsGA ENSP00000431637.1:n.*325_*326delinsGA
ENST00000578151.1:n.87_88delinsGA
ENST00000581221.5:n.267_268delinsGA
ENST00000583539.5:c.752_753delinsGA ENSP00000463121.1:p.Asp251Gly
ENST00000584617.5:c.474_475delinsGA
ENST00000584804.1:c.47_48delinsGA ENSP00000463658.1:p.Asp16Gly
ENST00000697678.1:n.654_655delinsGA
ENST00000697679.1:n.1826_1827delinsGA
ENST00000697680.1:c.*1616_*1617delinsGA ENSP00000513392.1:n.*1616_*1617delinsGA
ENST00000697681.1:c.*1913_*1914delinsGA ENSP00000513393.1:n.*1913_*1914delinsGA
ENST00000697683.1:c.*1616_*1617delinsGA ENSP00000513395.1:n.*1616_*1617delinsGA
ENST00000697684.1:n.812_813delinsGA
ENST00000697685.1:c.*1449_*1450delinsGA ENSP00000513396.1:n.*1449_*1450delinsGA
ENST00000697686.1:c.401_402delinsGA ENSP00000513397.1:p.Asp134Gly
ENST00000697687.1:n.631_632delinsGA
ENST00000697688.1:n.798_799delinsGA
ENST00000697689.1:c.*1288_*1289delinsGA ENSP00000513398.1:n.*1288_*1289delinsGA
ENST00000697690.1:c.752_753delinsGA ENSP00000513399.1:p.Asp251Gly
ENST00000697691.1:c.*724_*725delinsGA ENSP00000513400.1:n.*724_*725delinsGA
ENST00000697692.1:c.*764_*765delinsGA ENSP00000513401.1:n.*764_*765delinsGA
ENST00000697694.1:c.401_402delinsGA ENSP00000513402.1:p.Asp134Gly
ENST00000697695.1:n.1359_1360delinsGA
XM_006722001.2:c.752_753delinsGA XP_006722064.1:p.Asp251Gly
XM_006722001.4:c.752_753delinsGA XP_006722064.1:p.Asp251Gly
XM_006722002.2:c.752_753delinsGA XP_006722065.1:p.Asp251Gly
XM_006722002.4:c.752_753delinsGA XP_006722065.1:p.Asp251Gly
XM_006722004.2:c.401_402delinsGA XP_006722067.1:p.Asp134Gly
XM_006722004.3:c.401_402delinsGA XP_006722067.1:p.Asp134Gly
XM_006722005.2:c.401_402delinsGA XP_006722068.1:p.Asp134Gly
XM_006722005.3:c.401_402delinsGA XP_006722068.1:p.Asp134Gly
XM_011525092.1:c.401_402delinsGA XP_011523394.1:p.Asp134Gly
XM_011525092.2:c.401_402delinsGA XP_011523394.1:p.Asp134Gly
XM_011525093.1:c.401_402delinsGA XP_011523395.1:p.Asp134Gly
XM_011525093.2:c.401_402delinsGA XP_011523395.1:p.Asp134Gly
XM_011525094.1:c.401_402delinsGA XP_011523396.1:p.Asp134Gly
XM_011525094.2:c.401_402delinsGA XP_011523396.1:p.Asp134Gly
XM_017024914.1:c.401_402delinsGA XP_016880403.1:p.Asp134Gly
XM_017024915.1:c.401_402delinsGA XP_016880404.1:p.Asp134Gly
XM_017024916.1:c.401_402delinsGA XP_016880405.1:p.Asp134Gly
XM_017024917.1:c.401_402delinsGA XP_016880406.1:p.Asp134Gly
XM_017024918.2:c.401_402delinsGA XP_016880407.1:p.Asp134Gly
XM_017024919.1:c.401_402delinsGA XP_016880408.1:p.Asp134Gly
XR_934513.1:n.970_971delinsGA
XR_934513.3:n.1401_1402delinsGA
XR_934514.1:n.970_971delinsGA
XR_934514.3:n.1401_1402delinsGA