Canonical Allele Identifier: CA294121
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 141324
dbSNP Id: rs140804406

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703264C>T , CM000679.2:g.58703264C>T GRCh38
NC_000017.10:g.56780625C>T , CM000679.1:g.56780625C>T GRCh37
NC_000017.9:g.54135624C>T NCBI36
NG_023199.1:g.15663C>T , LRG_314:g.15663C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.289C>T ENSP00000464056.2:p.Arg97Cys
ENST00000697677.1:n.1721C>T
ENST00000697678.1:n.542C>T
ENST00000697679.1:n.1714C>T
ENST00000697680.1:c.*1504C>T ENSP00000513392.1:n.*1504C>T
ENST00000697681.1:c.*1656C>T ENSP00000513393.1:n.*1656C>T
ENST00000697683.1:c.*1504C>T ENSP00000513395.1:n.*1504C>T
ENST00000697684.1:n.700C>T
ENST00000697685.1:c.*1337C>T ENSP00000513396.1:n.*1337C>T
ENST00000697686.1:c.289C>T ENSP00000513397.1:p.Arg97Cys
ENST00000697687.1:n.519C>T
ENST00000697688.1:n.686C>T
ENST00000697689.1:c.*1176C>T ENSP00000513398.1:n.*1176C>T
ENST00000697690.1:c.640C>T ENSP00000513399.1:p.Arg214Cys
ENST00000697691.1:c.*612C>T ENSP00000513400.1:n.*612C>T
ENST00000697692.1:c.*652C>T ENSP00000513401.1:n.*652C>T
ENST00000697694.1:c.289C>T ENSP00000513402.1:p.Arg97Cys
ENST00000697695.1:n.1247C>T
ENST00000337432.9:c.640C>T MANE Select ENSP00000336701.4:p.Arg214Cys
ENST00000337432.8:c.640C>T ENSP00000336701.4:p.Arg214Cys
ENST00000413590.5:c.278C>T
ENST00000425173.5:c.436C>T ENSP00000407282.1:p.Arg146Cys
ENST00000461271.5:c.289C>T ENSP00000464056.1:p.Arg97Cys
ENST00000475762.5:c.*1343C>T ENSP00000432421.1:n.*1343C>T
ENST00000482007.5:c.*68C>T ENSP00000433332.1:n.*68C>T
ENST00000487525.5:c.*68C>T ENSP00000431637.1:n.*68C>T
ENST00000487921.5:n.552C>T
ENST00000583539.5:c.640C>T ENSP00000463121.1:p.Arg214Cys
ENST00000584617.5:c.362C>T
NM_058216.2:c.640C>T NP_478123.1:p.Arg214Cys
NR_103872.1:n.544C>T
XM_006722001.2:c.640C>T XP_006722064.1:p.Arg214Cys
XM_006722002.2:c.640C>T XP_006722065.1:p.Arg214Cys
XM_006722004.2:c.289C>T XP_006722067.1:p.Arg97Cys
XM_006722005.2:c.289C>T XP_006722068.1:p.Arg97Cys
XM_011525092.1:c.289C>T XP_011523394.1:p.Arg97Cys
XM_011525093.1:c.289C>T XP_011523395.1:p.Arg97Cys
XM_011525094.1:c.289C>T XP_011523396.1:p.Arg97Cys
XR_934513.1:n.713C>T
XR_934514.1:n.713C>T
XM_006722001.4:c.640C>T XP_006722064.1:p.Arg214Cys
XM_006722002.4:c.640C>T XP_006722065.1:p.Arg214Cys
XM_006722004.3:c.289C>T XP_006722067.1:p.Arg97Cys
XM_006722005.3:c.289C>T XP_006722068.1:p.Arg97Cys
XM_011525092.2:c.289C>T XP_011523394.1:p.Arg97Cys
XM_011525093.2:c.289C>T XP_011523395.1:p.Arg97Cys
XM_011525094.2:c.289C>T XP_011523396.1:p.Arg97Cys
XM_017024914.1:c.289C>T XP_016880403.1:p.Arg97Cys
XM_017024915.1:c.289C>T XP_016880404.1:p.Arg97Cys
XM_017024916.1:c.289C>T XP_016880405.1:p.Arg97Cys
XM_017024917.1:c.289C>T XP_016880406.1:p.Arg97Cys
XM_017024918.2:c.289C>T XP_016880407.1:p.Arg97Cys
XM_017024919.1:c.289C>T XP_016880408.1:p.Arg97Cys
XR_934513.3:n.1144C>T
XR_934514.3:n.1144C>T
NM_058216.3:c.640C>T MANE Select NP_478123.1:p.Arg214Cys
NR_103872.2:n.515C>T