Canonical Allele Identifier: CA3261180371
Community Standard Title: NM_058216.3(RAD51C):c.1075_1077delinsGCC (p.Thr359Ala)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734166_58734168delinsGCC , CM000679.2:g.58734166_58734168delinsGCC GRCh38
NC_000017.10:g.56811527_56811529delinsGCC , CM000679.1:g.56811527_56811529delinsGCC GRCh37
NC_000017.9:g.54166526_54166528delinsGCC NCBI36
NG_023199.1:g.46565_46567delinsGCC , LRG_314:g.46565_46567delinsGCC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1075_1077delinsGCC MANE Select NP_478123.1:p.Thr359Ala
ENST00000337432.9:c.1075_1077delinsGCC MANE Select ENSP00000336701.4:p.Thr359Ala
NM_058216.2:c.1075_1077delinsGCC NP_478123.1:p.Thr359Ala
NR_103872.1:n.979_981delinsGCC
NR_103872.2:n.950_952delinsGCC
ENST00000337432.8:c.1075_1077delinsGCC ENSP00000336701.4:p.Thr359Ala
ENST00000413590.5:c.716_718delinsGCC
ENST00000461271.6:c.*1607_*1609delinsGCC ENSP00000464056.2:n.*1607_*1609delinsGCC
ENST00000461706.1:n.262_264delinsGCC
ENST00000475762.5:c.*1711_*1713delinsGCC ENSP00000432421.1:n.*1711_*1713delinsGCC
ENST00000482007.5:c.*503_*505delinsGCC ENSP00000433332.1:n.*503_*505delinsGCC
ENST00000487525.5:c.*651_*653delinsGCC ENSP00000431637.1:n.*651_*653delinsGCC
ENST00000578151.1:n.288_290delinsGCC
ENST00000581221.5:n.590_592delinsGCC
ENST00000584804.1:c.309_311delinsGCC ENSP00000463658.1:p.Gln104Pro
ENST00000697680.1:c.*2039_*2041delinsGCC ENSP00000513392.1:n.*2039_*2041delinsGCC
ENST00000697681.1:c.*2236_*2238delinsGCC ENSP00000513393.1:n.*2236_*2238delinsGCC
ENST00000697683.1:c.*2011_*2013delinsGCC ENSP00000513395.1:n.*2011_*2013delinsGCC
ENST00000697685.1:c.*1772_*1774delinsGCC ENSP00000513396.1:n.*1772_*1774delinsGCC
ENST00000697686.1:c.846_848delinsGCC ENSP00000513397.1:p.Gln283Pro
ENST00000697689.1:c.*1489_*1491delinsGCC ENSP00000513398.1:n.*1489_*1491delinsGCC
ENST00000697690.1:c.*35_*37delinsGCC ENSP00000513399.1:n.*35_*37delinsGCC
ENST00000697691.1:c.*1047_*1049delinsGCC ENSP00000513400.1:n.*1047_*1049delinsGCC
ENST00000697692.1:c.*1087_*1089delinsGCC ENSP00000513401.1:n.*1087_*1089delinsGCC
ENST00000697694.1:c.724_726delinsGCC ENSP00000513402.1:p.Thr242Ala
ENST00000697695.1:n.1682_1684delinsGCC
XM_006722001.2:c.1078_1080delinsGCC XP_006722064.1:p.Thr360Ala
XM_006722001.4:c.1078_1080delinsGCC XP_006722064.1:p.Thr360Ala
XM_006722002.2:c.1014_1016delinsGCC XP_006722065.1:p.Gln339Pro
XM_006722002.4:c.1014_1016delinsGCC XP_006722065.1:p.Gln339Pro
XM_006722004.2:c.727_729delinsGCC XP_006722067.1:p.Thr243Ala
XM_006722004.3:c.727_729delinsGCC XP_006722067.1:p.Thr243Ala
XM_006722005.2:c.727_729delinsGCC XP_006722068.1:p.Thr243Ala
XM_006722005.3:c.727_729delinsGCC XP_006722068.1:p.Thr243Ala
XM_011525092.1:c.727_729delinsGCC XP_011523394.1:p.Thr243Ala
XM_011525092.2:c.727_729delinsGCC XP_011523394.1:p.Thr243Ala
XM_011525093.1:c.727_729delinsGCC XP_011523395.1:p.Thr243Ala
XM_011525093.2:c.727_729delinsGCC XP_011523395.1:p.Thr243Ala
XM_011525094.1:c.727_729delinsGCC XP_011523396.1:p.Thr243Ala
XM_011525094.2:c.727_729delinsGCC XP_011523396.1:p.Thr243Ala
XM_017024914.1:c.724_726delinsGCC XP_016880403.1:p.Thr242Ala
XM_017024915.1:c.724_726delinsGCC XP_016880404.1:p.Thr242Ala
XM_017024916.1:c.724_726delinsGCC XP_016880405.1:p.Thr242Ala
XM_017024917.1:c.724_726delinsGCC XP_016880406.1:p.Thr242Ala
XM_017024918.2:c.724_726delinsGCC XP_016880407.1:p.Thr242Ala
XM_017024919.1:c.663_665delinsGCC XP_016880408.1:p.Gln222Pro
XR_934513.1:n.1293_1295delinsGCC
XR_934513.3:n.1724_1726delinsGCC
XR_934514.1:n.1296_1298delinsGCC
XR_934514.3:n.1727_1729delinsGCC
XR_934886.1:n.149+3903_149+3905delinsGGC
XR_934886.2:n.149+3903_149+3905delinsGGC