Canonical Allele Identifier: CA16620494

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 418441
• ClinVar RCV Id: RCV000478459 ; RCV000566450 ; RCV000576215 ; RCV003334388
• dbSNP Id: rs767796996
• MyVariant Identifiers: chr17:g.56772550G>C (hg19) ; chr17:g.58695189G>C (hg38)
• PubMed: PMID:22451500 ; PMID:27622768

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58695189G>C , CM000679.2:g.58695189G>C	GRCh38
NC_000017.10:g.56772550G>C , CM000679.1:g.56772550G>C	GRCh37
NC_000017.9:g.54127549G>C	NCBI36
NG_023199.1:g.7588G>C , LRG_314:g.7588G>C
NG_047169.1:g.1891C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.53G>C	ENSP00000464056.2:p.Cys18Ser
ENST00000697675.1:n.1498G>C
ENST00000697676.1:n.464G>C
ENST00000697677.1:n.1485G>C
ENST00000697678.1:n.306G>C
ENST00000697679.1:n.1478G>C
ENST00000697680.1:c.*1268G>C	ENSP00000513392.1:n.*1268G>C
ENST00000697681.1:c.*1268G>C	ENSP00000513393.1:n.*1268G>C
ENST00000697683.1:c.*1268G>C	ENSP00000513395.1:n.*1268G>C
ENST00000697684.1:n.464G>C
ENST00000697685.1:c.*1268G>C	ENSP00000513396.1:n.*1268G>C
ENST00000697686.1:c.53G>C	ENSP00000513397.1:p.Cys18Ser
ENST00000697687.1:n.450G>C
ENST00000697688.1:n.450G>C
ENST00000697689.1:c.*1107G>C	ENSP00000513398.1:n.*1107G>C
ENST00000697690.1:c.404G>C	ENSP00000513399.1:p.Cys135Ser
ENST00000697691.1:c.*376G>C	ENSP00000513400.1:n.*376G>C
ENST00000697692.1:c.*416G>C	ENSP00000513401.1:n.*416G>C
ENST00000697693.1:n.1179G>C
ENST00000697694.1:c.53G>C	ENSP00000513402.1:p.Cys18Ser
ENST00000697695.1:n.1011G>C
ENST00000337432.9:c.404G>C MANE Select	ENSP00000336701.4:p.Cys135Ser
ENST00000337432.8:c.404G>C	ENSP00000336701.4:p.Cys135Ser
ENST00000413590.5:c.42G>C
ENST00000421782.3:c.404G>C	ENSP00000391450.2:p.Trp135Ser
ENST00000425173.5:c.200G>C	ENSP00000407282.1:p.Cys67Ser
ENST00000461271.5:c.53G>C	ENSP00000464056.1:p.Cys18Ser
ENST00000475762.5:c.*1107G>C	ENSP00000432421.1:n.*1107G>C
ENST00000482007.5:c.404G>C	ENSP00000433332.1:p.Ter135Ser
ENST00000486827.1:c.*1268G>C	ENSP00000436761.1:n.*1268G>C
ENST00000487525.5:c.404G>C	ENSP00000431637.1:p.Ter135Ser
ENST00000487921.5:n.316G>C
ENST00000583539.5:c.404G>C	ENSP00000463121.1:p.Cys135Ser
ENST00000584617.5:c.127-1504G>C
ENST00000622327.4:c.140G>C	ENSP00000482326.1:p.Cys47Ser
NM_002876.3:c.404G>C	NP_002867.1:p.Trp135Ser
NM_058216.2:c.404G>C	NP_478123.1:p.Cys135Ser
NR_103872.1:n.475G>C
NR_103873.1:n.372G>C
XM_006722001.2:c.404G>C	XP_006722064.1:p.Cys135Ser
XM_006722002.2:c.404G>C	XP_006722065.1:p.Cys135Ser
XM_006722004.2:c.53G>C	XP_006722067.1:p.Cys18Ser
XM_006722005.2:c.53G>C	XP_006722068.1:p.Cys18Ser
XM_011525092.1:c.53G>C	XP_011523394.1:p.Cys18Ser
XM_011525093.1:c.53G>C	XP_011523395.1:p.Cys18Ser
XM_011525094.1:c.53G>C	XP_011523396.1:p.Cys18Ser
XR_934513.1:n.477G>C
XR_934514.1:n.477G>C
XM_006722001.4:c.404G>C	XP_006722064.1:p.Cys135Ser
XM_006722002.4:c.404G>C	XP_006722065.1:p.Cys135Ser
XM_006722004.3:c.53G>C	XP_006722067.1:p.Cys18Ser
XM_006722005.3:c.53G>C	XP_006722068.1:p.Cys18Ser
XM_011525092.2:c.53G>C	XP_011523394.1:p.Cys18Ser
XM_011525093.2:c.53G>C	XP_011523395.1:p.Cys18Ser
XM_011525094.2:c.53G>C	XP_011523396.1:p.Cys18Ser
XM_017024914.1:c.53G>C	XP_016880403.1:p.Cys18Ser
XM_017024915.1:c.53G>C	XP_016880404.1:p.Cys18Ser
XM_017024916.1:c.53G>C	XP_016880405.1:p.Cys18Ser
XM_017024917.1:c.53G>C	XP_016880406.1:p.Cys18Ser
XM_017024918.2:c.53G>C	XP_016880407.1:p.Cys18Ser
XM_017024919.1:c.53G>C	XP_016880408.1:p.Cys18Ser
XR_934513.3:n.908G>C
XR_934514.3:n.908G>C
NM_058216.3:c.404G>C MANE Select	NP_478123.1:p.Cys135Ser
NR_103872.2:n.446G>C
NM_002876.4:c.404G>C	NP_002867.1:p.Trp135Ser