Canonical Allele Identifier: CA501074327
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 1567834
ClinVar RCV Id: RCV002210224
dbSNP Id: rs777585467

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692658G>T , CM000679.2:g.58692658G>T GRCh38
NC_000017.10:g.56770019G>T , CM000679.1:g.56770019G>T GRCh37
NC_000017.9:g.54125018G>T NCBI36
NG_023199.1:g.5057G>T , LRG_314:g.5057G>T
NG_047169.1:g.4422C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000461271.6:c.-234G>T ENSP00000464056.2:n.-234G>T
ENST00000697675.1:n.86G>T
ENST00000697676.1:n.75G>T
ENST00000697677.1:n.73G>T
ENST00000697678.1:n.47+26G>T
ENST00000697679.1:n.66G>T
ENST00000697680.1:c.15G>T ENSP00000513392.1:p.Thr5=
ENST00000697681.1:c.15G>T ENSP00000513393.1:p.Thr5=
ENST00000697683.1:c.15G>T ENSP00000513395.1:p.Thr5=
ENST00000697684.1:n.75G>T
ENST00000697685.1:c.15G>T ENSP00000513396.1:p.Thr5=
ENST00000697686.1:c.-207+26G>T ENSP00000513397.1:n.-207+26G>T
ENST00000697687.1:n.61G>T
ENST00000697688.1:n.61G>T
ENST00000697689.1:c.15G>T ENSP00000513398.1:p.Thr5=
ENST00000697690.1:c.15G>T ENSP00000513399.1:p.Thr5=
ENST00000697691.1:c.15G>T ENSP00000513400.1:p.Thr5=
ENST00000697692.1:c.15G>T ENSP00000513401.1:p.Thr5=
ENST00000337432.9:c.15G>T MANE Select ENSP00000336701.4:p.Thr5=
ENST00000337432.8:c.15G>T ENSP00000336701.4:p.Thr5=
ENST00000421782.3:c.15G>T ENSP00000391450.2:p.Thr5=
ENST00000461271.5:c.-234G>T ENSP00000464056.1:n.-234G>T
ENST00000475762.5:c.15G>T ENSP00000432421.1:p.Thr5=
ENST00000476741.2:n.57G>T
ENST00000482007.5:c.15G>T ENSP00000433332.1:p.Thr5=
ENST00000486827.1:c.15G>T ENSP00000436761.1:p.Thr5=
ENST00000487525.5:c.15G>T ENSP00000431637.1:p.Thr5=
ENST00000487921.5:n.57+26G>T
ENST00000583539.5:c.15G>T ENSP00000463121.1:p.Thr5=
NM_002876.3:c.15G>T NP_002867.1:p.Thr5=
NM_058216.2:c.15G>T NP_478123.1:p.Thr5=
NR_103872.1:n.86G>T
NR_103873.1:n.86G>T
XM_006722001.2:c.15G>T XP_006722064.1:p.Thr5=
XM_006722002.2:c.15G>T XP_006722065.1:p.Thr5=
XM_006722004.2:c.-234G>T XP_006722067.1:n.-234G>T
XM_006722005.2:c.-207+26G>T XP_006722068.1:n.-207+26G>T
XM_011525092.1:c.-534G>T XP_011523394.1:n.-534G>T
XM_011525093.1:c.-695G>T XP_011523395.1:n.-695G>T
XR_934513.1:n.88G>T
XR_934514.1:n.88G>T
XM_006722001.4:c.15G>T XP_006722064.1:p.Thr5=
XM_006722002.4:c.15G>T XP_006722065.1:p.Thr5=
XM_006722004.3:c.-234G>T XP_006722067.1:n.-234G>T
XM_006722005.3:c.-207+26G>T XP_006722068.1:n.-207+26G>T
XM_017024914.1:c.-234G>T XP_016880403.1:n.-234G>T
XM_017024916.1:c.-534G>T XP_016880405.1:n.-534G>T
XM_017024917.1:c.-207+26G>T XP_016880406.1:n.-207+26G>T
XM_017024918.2:c.-508G>T XP_016880407.1:n.-508G>T
XR_934513.3:n.519G>T
XR_934514.3:n.519G>T
NM_058216.3:c.15G>T MANE Select NP_478123.1:p.Thr5=
NR_103872.2:n.57G>T
NM_002876.4:c.15G>T NP_002867.1:p.Thr5=