Canonical Allele Identifier: CA193384
Gene: RAD51C HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 185920
ClinVar RCV Id: RCV000165425
dbSNP Id: rs786202563

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58695001_58695005del , CM000679.2:g.58695001_58695005del GRCh38
NC_000017.10:g.56772362_56772366del , CM000679.1:g.56772362_56772366del GRCh37
NC_000017.9:g.54127361_54127365del NCBI36
NG_023199.1:g.7400_7404del , LRG_314:g.7400_7404del
NG_047169.1:g.2077_2081del

Transcript Alleles

HGVS Amino-acid change
NM_002876.3:c.216_220del VV NP_002867.1:p.Pro73IlefsTer6
NM_058216.2:c.216_220del VV NP_478123.1:p.Pro73IlefsTer6
NR_103872.1:n.287_291del
NR_103873.1:n.184_188del
XM_006722001.2:c.216_220del XP_006722064.1:p.Pro73IlefsTer6
XM_006722002.2:c.216_220del XP_006722065.1:p.Pro73IlefsTer6
XM_006722004.2:c.-136_-132del XP_006722067.1:p.=
XM_006722005.2:c.-136_-132del XP_006722068.1:p.=
XM_011525092.1:c.-136_-132del XP_011523394.1:p.=
XM_011525093.1:c.-136_-132del XP_011523395.1:p.=
XM_011525094.1:c.-136_-132del XP_011523396.1:p.=
XR_934513.1:n.289_293del
XR_934514.1:n.289_293del
XM_006722001.4:c.216_220del XP_006722064.1:p.Pro73IlefsTer6
XM_006722002.4:c.216_220del XP_006722065.1:p.Pro73IlefsTer6
XM_006722004.3:c.-136_-132del XP_006722067.1:p.=
XM_006722005.3:c.-136_-132del XP_006722068.1:p.=
XM_011525092.2:c.-136_-132del XP_011523394.1:p.=
XM_011525093.2:c.-136_-132del XP_011523395.1:p.=
XM_011525094.2:c.-136_-132del XP_011523396.1:p.=
XM_017024914.1:c.-136_-132del XP_016880403.1:p.=
XM_017024915.1:c.-136_-132del XP_016880404.1:p.=
XM_017024916.1:c.-136_-132del XP_016880405.1:p.=
XM_017024917.1:c.-136_-132del XP_016880406.1:p.=
XM_017024918.2:c.-136_-132del XP_016880407.1:p.=
XM_017024919.1:c.-136_-132del XP_016880408.1:p.=
XR_934513.3:n.720_724del
XR_934514.3:n.720_724del
NM_058216.3:c.216_220del VV MANE Preferred NP_478123.1:p.Pro73IlefsTer6
ENST00000337432.8:c.216_220del ENSP00000336701.4:p.Pro73IlefsTer6
ENST00000421782.3:c.216_220del ENSP00000391450.2:p.Pro73IlefsTer6
ENST00000425173.5:n.12_16del ENSP00000407282.1:p.Pro5IlefsTer6
ENST00000461271.5:c.-136_-132del ENSP00000464056.1:p.=
ENST00000475762.5:c.*919_*923del ENSP00000432421.1:p.=
ENST00000482007.5:c.216_220del ENSP00000433332.1:p.Pro73IlefsTer6
ENST00000486827.1:c.*1080_*1084del ENSP00000436761.1:p.=
ENST00000487525.5:c.216_220del ENSP00000431637.1:p.Pro73IlefsTer6
ENST00000487921.5:n.128_132del
ENST00000583539.5:c.216_220del ENSP00000463121.1:p.Pro73IlefsTer6
ENST00000584617.5:n.127-1692_127-1688del