Canonical Allele Identifier: CA985028335
Gene: RAD51C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703373_58703376del , CM000679.2:g.58703373_58703376del GRCh38
NC_000017.10:g.56780734_56780737del , CM000679.1:g.56780734_56780737del GRCh37
NC_000017.9:g.54135733_54135736del NCBI36
NG_023199.1:g.15772_15775del , LRG_314:g.15772_15775del

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.354+44_354+47del ENSP00000464056.2:n.354+44_354+47del
ENST00000697677.1:n.1830_1833del
ENST00000697678.1:n.607+44_607+47del
ENST00000697679.1:n.1779+44_1779+47del
ENST00000697680.1:c.*1569+44_*1569+47del ENSP00000513392.1:n.*1569+44_*1569+47del
ENST00000697681.1:c.*1721+44_*1721+47del ENSP00000513393.1:n.*1721+44_*1721+47del
ENST00000697683.1:c.*1569+44_*1569+47del ENSP00000513395.1:n.*1569+44_*1569+47del
ENST00000697684.1:n.765+44_765+47del
ENST00000697685.1:c.*1402+44_*1402+47del ENSP00000513396.1:n.*1402+44_*1402+47del
ENST00000697686.1:c.354+44_354+47del ENSP00000513397.1:n.354+44_354+47del
ENST00000697687.1:n.584+44_584+47del
ENST00000697688.1:n.751+44_751+47del
ENST00000697689.1:c.*1241+44_*1241+47del ENSP00000513398.1:n.*1241+44_*1241+47del
ENST00000697690.1:c.705+44_705+47del ENSP00000513399.1:n.705+44_705+47del
ENST00000697691.1:c.*677+44_*677+47del ENSP00000513400.1:n.*677+44_*677+47del
ENST00000697692.1:c.*717+44_*717+47del ENSP00000513401.1:n.*717+44_*717+47del
ENST00000697694.1:c.354+44_354+47del ENSP00000513402.1:n.354+44_354+47del
ENST00000697695.1:n.1312+44_1312+47del
ENST00000337432.9:c.705+44_705+47del MANE Select ENSP00000336701.4:n.705+44_705+47del
ENST00000337432.8:c.705+44_705+47del ENSP00000336701.4:n.705+44_705+47del
ENST00000413590.5:c.343+44_343+47del
ENST00000425173.5:c.501+44_501+47del ENSP00000407282.1:n.501+44_501+47del
ENST00000461271.5:c.354+44_354+47del ENSP00000464056.1:n.354+44_354+47del
ENST00000475762.5:c.*1408+44_*1408+47del ENSP00000432421.1:n.*1408+44_*1408+47del
ENST00000482007.5:c.*133+44_*133+47del ENSP00000433332.1:n.*133+44_*133+47del
ENST00000487525.5:c.*133+44_*133+47del ENSP00000431637.1:n.*133+44_*133+47del
ENST00000487921.5:n.617+44_617+47del
ENST00000583539.5:c.705+44_705+47del ENSP00000463121.1:n.705+44_705+47del
ENST00000584617.5:c.427+44_427+47del
NM_058216.2:c.705+44_705+47del NP_478123.1:n.705+44_705+47del
NR_103872.1:n.609+44_609+47del
XM_006722001.2:c.705+44_705+47del XP_006722064.1:n.705+44_705+47del
XM_006722002.2:c.705+44_705+47del XP_006722065.1:n.705+44_705+47del
XM_006722004.2:c.354+44_354+47del XP_006722067.1:n.354+44_354+47del
XM_006722005.2:c.354+44_354+47del XP_006722068.1:n.354+44_354+47del
XM_011525092.1:c.354+44_354+47del XP_011523394.1:n.354+44_354+47del
XM_011525093.1:c.354+44_354+47del XP_011523395.1:n.354+44_354+47del
XM_011525094.1:c.354+44_354+47del XP_011523396.1:n.354+44_354+47del
XR_934513.1:n.778+44_778+47del
XR_934514.1:n.778+44_778+47del
XM_006722001.4:c.705+44_705+47del XP_006722064.1:n.705+44_705+47del
XM_006722002.4:c.705+44_705+47del XP_006722065.1:n.705+44_705+47del
XM_006722004.3:c.354+44_354+47del XP_006722067.1:n.354+44_354+47del
XM_006722005.3:c.354+44_354+47del XP_006722068.1:n.354+44_354+47del
XM_011525092.2:c.354+44_354+47del XP_011523394.1:n.354+44_354+47del
XM_011525093.2:c.354+44_354+47del XP_011523395.1:n.354+44_354+47del
XM_011525094.2:c.354+44_354+47del XP_011523396.1:n.354+44_354+47del
XM_017024914.1:c.354+44_354+47del XP_016880403.1:n.354+44_354+47del
XM_017024915.1:c.354+44_354+47del XP_016880404.1:n.354+44_354+47del
XM_017024916.1:c.354+44_354+47del XP_016880405.1:n.354+44_354+47del
XM_017024917.1:c.354+44_354+47del XP_016880406.1:n.354+44_354+47del
XM_017024918.2:c.354+44_354+47del XP_016880407.1:n.354+44_354+47del
XM_017024919.1:c.354+44_354+47del XP_016880408.1:n.354+44_354+47del
XR_934513.3:n.1209+44_1209+47del
XR_934514.3:n.1209+44_1209+47del
NM_058216.3:c.705+44_705+47del MANE Select NP_478123.1:n.705+44_705+47del
NR_103872.2:n.580+44_580+47del