Canonical Allele Identifier: CA3261179495
Community Standard Title: NM_058216.3(RAD51C):c.758_759delinsGC (p.Asp253Gly)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709911_58709912delinsGC , CM000679.2:g.58709911_58709912delinsGC GRCh38
NC_000017.10:g.56787272_56787273delinsGC , CM000679.1:g.56787272_56787273delinsGC GRCh37
NC_000017.9:g.54142271_54142272delinsGC NCBI36
NG_023199.1:g.22310_22311delinsGC , LRG_314:g.22310_22311delinsGC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.758_759delinsGC MANE Select NP_478123.1:p.Asp253Gly
ENST00000337432.9:c.758_759delinsGC MANE Select ENSP00000336701.4:p.Asp253Gly
NM_058216.2:c.758_759delinsGC NP_478123.1:p.Asp253Gly
NR_103872.1:n.662_663delinsGC
NR_103872.2:n.633_634delinsGC
ENST00000337432.8:c.758_759delinsGC ENSP00000336701.4:p.Asp253Gly
ENST00000413590.5:c.396_397delinsGC
ENST00000461271.6:c.407_408delinsGC ENSP00000464056.2:p.Asp136Gly
ENST00000475762.5:c.*1461_*1462delinsGC ENSP00000432421.1:n.*1461_*1462delinsGC
ENST00000482007.5:c.*186_*187delinsGC ENSP00000433332.1:n.*186_*187delinsGC
ENST00000487525.5:c.*331_*332delinsGC ENSP00000431637.1:n.*331_*332delinsGC
ENST00000578151.1:n.93_94delinsGC
ENST00000581221.5:n.273_274delinsGC
ENST00000583539.5:c.758_759delinsGC ENSP00000463121.1:p.Asp253Gly
ENST00000584617.5:c.480_481delinsGC
ENST00000584804.1:c.53_54delinsGC ENSP00000463658.1:p.Asp18Gly
ENST00000697678.1:n.660_661delinsGC
ENST00000697679.1:n.1832_1833delinsGC
ENST00000697680.1:c.*1622_*1623delinsGC ENSP00000513392.1:n.*1622_*1623delinsGC
ENST00000697681.1:c.*1919_*1920delinsGC ENSP00000513393.1:n.*1919_*1920delinsGC
ENST00000697683.1:c.*1622_*1623delinsGC ENSP00000513395.1:n.*1622_*1623delinsGC
ENST00000697684.1:n.818_819delinsGC
ENST00000697685.1:c.*1455_*1456delinsGC ENSP00000513396.1:n.*1455_*1456delinsGC
ENST00000697686.1:c.407_408delinsGC ENSP00000513397.1:p.Asp136Gly
ENST00000697687.1:n.637_638delinsGC
ENST00000697688.1:n.804_805delinsGC
ENST00000697689.1:c.*1294_*1295delinsGC ENSP00000513398.1:n.*1294_*1295delinsGC
ENST00000697690.1:c.758_759delinsGC ENSP00000513399.1:p.Asp253Gly
ENST00000697691.1:c.*730_*731delinsGC ENSP00000513400.1:n.*730_*731delinsGC
ENST00000697692.1:c.*770_*771delinsGC ENSP00000513401.1:n.*770_*771delinsGC
ENST00000697694.1:c.407_408delinsGC ENSP00000513402.1:p.Asp136Gly
ENST00000697695.1:n.1365_1366delinsGC
XM_006722001.2:c.758_759delinsGC XP_006722064.1:p.Asp253Gly
XM_006722001.4:c.758_759delinsGC XP_006722064.1:p.Asp253Gly
XM_006722002.2:c.758_759delinsGC XP_006722065.1:p.Asp253Gly
XM_006722002.4:c.758_759delinsGC XP_006722065.1:p.Asp253Gly
XM_006722004.2:c.407_408delinsGC XP_006722067.1:p.Asp136Gly
XM_006722004.3:c.407_408delinsGC XP_006722067.1:p.Asp136Gly
XM_006722005.2:c.407_408delinsGC XP_006722068.1:p.Asp136Gly
XM_006722005.3:c.407_408delinsGC XP_006722068.1:p.Asp136Gly
XM_011525092.1:c.407_408delinsGC XP_011523394.1:p.Asp136Gly
XM_011525092.2:c.407_408delinsGC XP_011523394.1:p.Asp136Gly
XM_011525093.1:c.407_408delinsGC XP_011523395.1:p.Asp136Gly
XM_011525093.2:c.407_408delinsGC XP_011523395.1:p.Asp136Gly
XM_011525094.1:c.407_408delinsGC XP_011523396.1:p.Asp136Gly
XM_011525094.2:c.407_408delinsGC XP_011523396.1:p.Asp136Gly
XM_017024914.1:c.407_408delinsGC XP_016880403.1:p.Asp136Gly
XM_017024915.1:c.407_408delinsGC XP_016880404.1:p.Asp136Gly
XM_017024916.1:c.407_408delinsGC XP_016880405.1:p.Asp136Gly
XM_017024917.1:c.407_408delinsGC XP_016880406.1:p.Asp136Gly
XM_017024918.2:c.407_408delinsGC XP_016880407.1:p.Asp136Gly
XM_017024919.1:c.407_408delinsGC XP_016880408.1:p.Asp136Gly
XR_934513.1:n.976_977delinsGC
XR_934513.3:n.1407_1408delinsGC
XR_934514.1:n.976_977delinsGC
XR_934514.3:n.1407_1408delinsGC