Canonical Allele Identifier: CA3261180930
Community Standard Title: NM_058216.3(RAD51C):c.467_468delinsAC (p.Val156Asp)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58696755_58696756delinsAC , CM000679.2:g.58696755_58696756delinsAC GRCh38
NC_000017.10:g.56774116_56774117delinsAC , CM000679.1:g.56774116_56774117delinsAC GRCh37
NC_000017.9:g.54129115_54129116delinsAC NCBI36
NG_023199.1:g.9154_9155delinsAC , LRG_314:g.9154_9155delinsAC
NG_047169.1:g.324_325delinsGT

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.467_468delinsAC MANE Select NP_478123.1:p.Val156Asp
ENST00000337432.9:c.467_468delinsAC MANE Select ENSP00000336701.4:p.Val156Asp
NM_058216.2:c.467_468delinsAC NP_478123.1:p.Val156Asp
NR_103872.1:n.475+1566_475+1567delinsAC
NR_103872.2:n.446+1566_446+1567delinsAC
ENST00000337432.8:c.467_468delinsAC ENSP00000336701.4:p.Val156Asp
ENST00000413590.5:c.105_106delinsAC
ENST00000425173.5:c.263_264delinsAC ENSP00000407282.1:p.Val88Asp
ENST00000461271.5:c.116_117delinsAC ENSP00000464056.1:p.Val39Asp
ENST00000461271.6:c.116_117delinsAC ENSP00000464056.2:p.Val39Asp
ENST00000475762.5:c.*1170_*1171delinsAC ENSP00000432421.1:n.*1170_*1171delinsAC
ENST00000482007.5:c.404+1566_404+1567delinsAC ENSP00000433332.1:n.404+1566_404+1567delinsAC
ENST00000487525.5:c.404+1566_404+1567delinsAC ENSP00000431637.1:n.404+1566_404+1567delinsAC
ENST00000487921.5:n.379_380delinsAC
ENST00000583539.5:c.467_468delinsAC ENSP00000463121.1:p.Val156Asp
ENST00000584617.5:c.189_190delinsAC
ENST00000622327.4:c.203_204delinsAC ENSP00000482326.1:p.Val68Asp
ENST00000697675.1:n.3064_3065delinsAC
ENST00000697676.1:n.527_528delinsAC
ENST00000697677.1:n.1548_1549delinsAC
ENST00000697678.1:n.369_370delinsAC
ENST00000697679.1:n.1541_1542delinsAC
ENST00000697680.1:c.*1331_*1332delinsAC ENSP00000513392.1:n.*1331_*1332delinsAC
ENST00000697681.1:c.*1358_*1359delinsAC ENSP00000513393.1:n.*1358_*1359delinsAC
ENST00000697683.1:c.*1331_*1332delinsAC ENSP00000513395.1:n.*1331_*1332delinsAC
ENST00000697684.1:n.527_528delinsAC
ENST00000697685.1:c.*1268+1566_*1268+1567delinsAC ENSP00000513396.1:n.*1268+1566_*1268+1567delinsAC
ENST00000697686.1:c.116_117delinsAC ENSP00000513397.1:p.Val39Asp
ENST00000697687.1:n.450+1566_450+1567delinsAC
ENST00000697688.1:n.513_514delinsAC
ENST00000697689.1:c.*1107+1566_*1107+1567delinsAC ENSP00000513398.1:n.*1107+1566_*1107+1567delinsAC
ENST00000697690.1:c.467_468delinsAC ENSP00000513399.1:p.Val156Asp
ENST00000697691.1:c.*439_*440delinsAC ENSP00000513400.1:n.*439_*440delinsAC
ENST00000697692.1:c.*479_*480delinsAC ENSP00000513401.1:n.*479_*480delinsAC
ENST00000697694.1:c.116_117delinsAC ENSP00000513402.1:p.Val39Asp
ENST00000697695.1:n.1074_1075delinsAC
XM_006722001.2:c.467_468delinsAC XP_006722064.1:p.Val156Asp
XM_006722001.4:c.467_468delinsAC XP_006722064.1:p.Val156Asp
XM_006722002.2:c.467_468delinsAC XP_006722065.1:p.Val156Asp
XM_006722002.4:c.467_468delinsAC XP_006722065.1:p.Val156Asp
XM_006722004.2:c.116_117delinsAC XP_006722067.1:p.Val39Asp
XM_006722004.3:c.116_117delinsAC XP_006722067.1:p.Val39Asp
XM_006722005.2:c.116_117delinsAC XP_006722068.1:p.Val39Asp
XM_006722005.3:c.116_117delinsAC XP_006722068.1:p.Val39Asp
XM_011525092.1:c.116_117delinsAC XP_011523394.1:p.Val39Asp
XM_011525092.2:c.116_117delinsAC XP_011523394.1:p.Val39Asp
XM_011525093.1:c.116_117delinsAC XP_011523395.1:p.Val39Asp
XM_011525093.2:c.116_117delinsAC XP_011523395.1:p.Val39Asp
XM_011525094.1:c.116_117delinsAC XP_011523396.1:p.Val39Asp
XM_011525094.2:c.116_117delinsAC XP_011523396.1:p.Val39Asp
XM_017024914.1:c.116_117delinsAC XP_016880403.1:p.Val39Asp
XM_017024915.1:c.116_117delinsAC XP_016880404.1:p.Val39Asp
XM_017024916.1:c.116_117delinsAC XP_016880405.1:p.Val39Asp
XM_017024917.1:c.116_117delinsAC XP_016880406.1:p.Val39Asp
XM_017024918.2:c.116_117delinsAC XP_016880407.1:p.Val39Asp
XM_017024919.1:c.116_117delinsAC XP_016880408.1:p.Val39Asp
XR_934513.1:n.540_541delinsAC
XR_934513.3:n.971_972delinsAC
XR_934514.1:n.540_541delinsAC
XR_934514.3:n.971_972delinsAC