Canonical Allele Identifier: CA16620492

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 420040
• ClinVar RCV Id: RCV000480944 ; RCV000569826 ; RCV000698641
• dbSNP Id: rs1064794253
• gnomAD v4: 17-58695090-CCTT-C
• MyVariant Identifiers: chr17:g.56772454_56772456del (hg19) ; chr17:g.58695093_58695095del (hg38)
• PubMed: PMID:21990120

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58695093_58695095del , CM000679.2:g.58695093_58695095del	GRCh38
NC_000017.10:g.56772454_56772456del , CM000679.1:g.56772454_56772456del	GRCh37
NC_000017.9:g.54127453_54127455del	NCBI36
NG_023199.1:g.7492_7494del , LRG_314:g.7492_7494del
NG_047169.1:g.1987_1989del

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.-44_-42del	ENSP00000464056.2:n.-44_-42del
ENST00000697675.1:n.1402_1404del
ENST00000697676.1:n.368_370del
ENST00000697677.1:n.1389_1391del
ENST00000697678.1:n.210_212del
ENST00000697679.1:n.1382_1384del
ENST00000697680.1:c.*1172_*1174del	ENSP00000513392.1:n.*1172_*1174del
ENST00000697681.1:c.*1172_*1174del	ENSP00000513393.1:n.*1172_*1174del
ENST00000697683.1:c.*1172_*1174del	ENSP00000513395.1:n.*1172_*1174del
ENST00000697684.1:n.368_370del
ENST00000697685.1:c.*1172_*1174del	ENSP00000513396.1:n.*1172_*1174del
ENST00000697686.1:c.-44_-42del	ENSP00000513397.1:n.-44_-42del
ENST00000697687.1:n.354_356del
ENST00000697688.1:n.354_356del
ENST00000697689.1:c.*1011_*1013del	ENSP00000513398.1:n.*1011_*1013del
ENST00000697690.1:c.308_310del	ENSP00000513399.1:p.Phe103del
ENST00000697691.1:c.*280_*282del	ENSP00000513400.1:n.*280_*282del
ENST00000697692.1:c.*320_*322del	ENSP00000513401.1:n.*320_*322del
ENST00000697693.1:n.1083_1085del
ENST00000697694.1:c.-44_-42del	ENSP00000513402.1:n.-44_-42del
ENST00000697695.1:n.915_917del
ENST00000337432.9:c.308_310del MANE Select	ENSP00000336701.4:p.Phe103del
ENST00000337432.8:c.308_310del	ENSP00000336701.4:p.Phe103del
ENST00000421782.3:c.308_310del	ENSP00000391450.2:p.Phe103del
ENST00000425173.5:c.104_106del	ENSP00000407282.1:p.Phe35del
ENST00000461271.5:c.-44_-42del	ENSP00000464056.1:n.-44_-42del
ENST00000475762.5:c.*1011_*1013del	ENSP00000432421.1:n.*1011_*1013del
ENST00000482007.5:c.308_310del	ENSP00000433332.1:p.Phe103del
ENST00000486827.1:c.*1172_*1174del	ENSP00000436761.1:n.*1172_*1174del
ENST00000487525.5:c.308_310del	ENSP00000431637.1:p.Phe103del
ENST00000487921.5:n.220_222del
ENST00000583539.5:c.308_310del	ENSP00000463121.1:p.Phe103del
ENST00000584617.5:c.127-1600_127-1598del
ENST00000622327.4:c.44_46del	ENSP00000482326.1:p.Phe15del
NM_002876.3:c.308_310del	NP_002867.1:p.Phe103del
NM_058216.2:c.308_310del	NP_478123.1:p.Phe103del
NR_103872.1:n.379_381del
NR_103873.1:n.276_278del
XM_006722001.2:c.308_310del	XP_006722064.1:p.Phe103del
XM_006722002.2:c.308_310del	XP_006722065.1:p.Phe103del
XM_006722004.2:c.-44_-42del	XP_006722067.1:n.-44_-42del
XM_006722005.2:c.-44_-42del	XP_006722068.1:n.-44_-42del
XM_011525092.1:c.-44_-42del	XP_011523394.1:n.-44_-42del
XM_011525093.1:c.-44_-42del	XP_011523395.1:n.-44_-42del
XM_011525094.1:c.-44_-42del	XP_011523396.1:n.-44_-42del
XR_934513.1:n.381_383del
XR_934514.1:n.381_383del
XM_006722001.4:c.308_310del	XP_006722064.1:p.Phe103del
XM_006722002.4:c.308_310del	XP_006722065.1:p.Phe103del
XM_006722004.3:c.-44_-42del	XP_006722067.1:n.-44_-42del
XM_006722005.3:c.-44_-42del	XP_006722068.1:n.-44_-42del
XM_011525092.2:c.-44_-42del	XP_011523394.1:n.-44_-42del
XM_011525093.2:c.-44_-42del	XP_011523395.1:n.-44_-42del
XM_011525094.2:c.-44_-42del	XP_011523396.1:n.-44_-42del
XM_017024914.1:c.-44_-42del	XP_016880403.1:n.-44_-42del
XM_017024915.1:c.-44_-42del	XP_016880404.1:n.-44_-42del
XM_017024916.1:c.-44_-42del	XP_016880405.1:n.-44_-42del
XM_017024917.1:c.-44_-42del	XP_016880406.1:n.-44_-42del
XM_017024918.2:c.-44_-42del	XP_016880407.1:n.-44_-42del
XM_017024919.1:c.-44_-42del	XP_016880408.1:n.-44_-42del
XR_934513.3:n.812_814del
XR_934514.3:n.812_814del
NM_058216.3:c.308_310del MANE Select	NP_478123.1:p.Phe103del
NR_103872.2:n.350_352del
NM_002876.4:c.308_310del	NP_002867.1:p.Phe103del