Canonical Allele Identifier: CA2267819429
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703181_58703182delinsGT , CM000679.2:g.58703181_58703182delinsGT GRCh38
NC_000017.10:g.56780542_56780543delinsGT , CM000679.1:g.56780542_56780543delinsGT GRCh37
NC_000017.9:g.54135541_54135542delinsGT NCBI36
NG_023199.1:g.15580_15581delinsGT , LRG_314:g.15580_15581delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000461271.6:c.221-15_221-14delinsGT ENSP00000464056.2:n.221-15_221-14delinsGT...
ENST00000697677.1:n.1653-15_1653-14delinsGT
ENST00000697678.1:n.474-15_474-14delinsGT
ENST00000697679.1:n.1646-15_1646-14delinsGT
ENST00000697680.1:c.*1436-15_*1436-14delinsGT ENSP00000513392.1:n.*1436-15_*1436-14deli...
ENST00000697681.1:c.*1588-15_*1588-14delinsGT ENSP00000513393.1:n.*1588-15_*1588-14deli...
ENST00000697683.1:c.*1436-15_*1436-14delinsGT ENSP00000513395.1:n.*1436-15_*1436-14deli...
ENST00000697684.1:n.632-15_632-14delinsGT
ENST00000697685.1:c.*1269-15_*1269-14delinsGT ENSP00000513396.1:n.*1269-15_*1269-14deli...
ENST00000697686.1:c.221-15_221-14delinsGT ENSP00000513397.1:n.221-15_221-14delinsGT...
ENST00000697687.1:n.451-15_451-14delinsGT
ENST00000697688.1:n.618-15_618-14delinsGT
ENST00000697689.1:c.*1108-15_*1108-14delinsGT ENSP00000513398.1:n.*1108-15_*1108-14deli...
ENST00000697690.1:c.572-15_572-14delinsGT ENSP00000513399.1:n.572-15_572-14delinsGT...
ENST00000697691.1:c.*544-15_*544-14delinsGT ENSP00000513400.1:n.*544-15_*544-14delins...
ENST00000697692.1:c.*584-15_*584-14delinsGT ENSP00000513401.1:n.*584-15_*584-14delins...
ENST00000697694.1:c.221-15_221-14delinsGT ENSP00000513402.1:n.221-15_221-14delinsGT...
ENST00000697695.1:n.1179-15_1179-14delinsGT
ENST00000337432.9:c.572-15_572-14delinsGT MANE Select ENSP00000336701.4:n.572-15_572-14delinsGT...
ENST00000337432.8:c.572-15_572-14delinsGT ENSP00000336701.4:n.572-15_572-14delinsGT...
ENST00000413590.5:c.210-15_210-14delinsGT
ENST00000425173.5:c.368-15_368-14delinsGT ENSP00000407282.1:n.368-15_368-14delinsGT...
ENST00000461271.5:c.221-15_221-14delinsGT ENSP00000464056.1:n.221-15_221-14delinsGT...
ENST00000475762.5:c.*1275-15_*1275-14delinsGT ENSP00000432421.1:n.*1275-15_*1275-14deli...
ENST00000482007.5:c.405-15_405-14delinsGT ENSP00000433332.1:n.405-15_405-14delinsGT...
ENST00000487525.5:c.405-15_405-14delinsGT ENSP00000431637.1:n.405-15_405-14delinsGT...
ENST00000487921.5:n.484-15_484-14delinsGT
ENST00000583539.5:c.572-15_572-14delinsGT ENSP00000463121.1:n.572-15_572-14delinsGT...
ENST00000584617.5:c.294-15_294-14delinsGT
NM_058216.2:c.572-15_572-14delinsGT NP_478123.1:n.572-15_572-14delinsGT
NR_103872.1:n.476-15_476-14delinsGT
XM_006722001.2:c.572-15_572-14delinsGT XP_006722064.1:n.572-15_572-14delinsGT
XM_006722002.2:c.572-15_572-14delinsGT XP_006722065.1:n.572-15_572-14delinsGT
XM_006722004.2:c.221-15_221-14delinsGT XP_006722067.1:n.221-15_221-14delinsGT
XM_006722005.2:c.221-15_221-14delinsGT XP_006722068.1:n.221-15_221-14delinsGT
XM_011525092.1:c.221-15_221-14delinsGT XP_011523394.1:n.221-15_221-14delinsGT
XM_011525093.1:c.221-15_221-14delinsGT XP_011523395.1:n.221-15_221-14delinsGT
XM_011525094.1:c.221-15_221-14delinsGT XP_011523396.1:n.221-15_221-14delinsGT
XR_934513.1:n.645-15_645-14delinsGT
XR_934514.1:n.645-15_645-14delinsGT
XM_006722001.4:c.572-15_572-14delinsGT XP_006722064.1:n.572-15_572-14delinsGT
XM_006722002.4:c.572-15_572-14delinsGT XP_006722065.1:n.572-15_572-14delinsGT
XM_006722004.3:c.221-15_221-14delinsGT XP_006722067.1:n.221-15_221-14delinsGT
XM_006722005.3:c.221-15_221-14delinsGT XP_006722068.1:n.221-15_221-14delinsGT
XM_011525092.2:c.221-15_221-14delinsGT XP_011523394.1:n.221-15_221-14delinsGT
XM_011525093.2:c.221-15_221-14delinsGT XP_011523395.1:n.221-15_221-14delinsGT
XM_011525094.2:c.221-15_221-14delinsGT XP_011523396.1:n.221-15_221-14delinsGT
XM_017024914.1:c.221-15_221-14delinsGT XP_016880403.1:n.221-15_221-14delinsGT
XM_017024915.1:c.221-15_221-14delinsGT XP_016880404.1:n.221-15_221-14delinsGT
XM_017024916.1:c.221-15_221-14delinsGT XP_016880405.1:n.221-15_221-14delinsGT
XM_017024917.1:c.221-15_221-14delinsGT XP_016880406.1:n.221-15_221-14delinsGT
XM_017024918.2:c.221-15_221-14delinsGT XP_016880407.1:n.221-15_221-14delinsGT
XM_017024919.1:c.221-15_221-14delinsGT XP_016880408.1:n.221-15_221-14delinsGT
XR_934513.3:n.1076-15_1076-14delinsGT
XR_934514.3:n.1076-15_1076-14delinsGT
NM_058216.3:c.572-15_572-14delinsGT MANE Select NP_478123.1:n.572-15_572-14delinsGT
NR_103872.2:n.447-15_447-14delinsGT