Canonical Allele Identifier: CA658658643

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 484742
• ClinVar RCV Id: RCV000568747 ; RCV004024504
• dbSNP Id: rs1555597132
• MyVariant Identifiers: chr17:g.56780610_56780613del (hg19) ; chr17:g.58703249_58703252del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703249_58703252del , CM000679.2:g.58703249_58703252del	GRCh38
NC_000017.10:g.56780610_56780613del , CM000679.1:g.56780610_56780613del	GRCh37
NC_000017.9:g.54135609_54135612del	NCBI36
NG_023199.1:g.15648_15651del , LRG_314:g.15648_15651del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.274_277del	ENSP00000464056.2:p.Tyr92IlefsTer29
ENST00000697677.1:n.1706_1709del
ENST00000697678.1:n.527_530del
ENST00000697679.1:n.1699_1702del
ENST00000697680.1:c.*1489_*1492del	ENSP00000513392.1:n.*1489_*1492del
ENST00000697681.1:c.*1641_*1644del	ENSP00000513393.1:n.*1641_*1644del
ENST00000697683.1:c.*1489_*1492del	ENSP00000513395.1:n.*1489_*1492del
ENST00000697684.1:n.685_688del
ENST00000697685.1:c.*1322_*1325del	ENSP00000513396.1:n.*1322_*1325del
ENST00000697686.1:c.274_277del	ENSP00000513397.1:p.Tyr92IlefsTer29
ENST00000697687.1:n.504_507del
ENST00000697688.1:n.671_674del
ENST00000697689.1:c.*1161_*1164del	ENSP00000513398.1:n.*1161_*1164del
ENST00000697690.1:c.625_628del	ENSP00000513399.1:p.Tyr209IlefsTer29
ENST00000697691.1:c.*597_*600del	ENSP00000513400.1:n.*597_*600del
ENST00000697692.1:c.*637_*640del	ENSP00000513401.1:n.*637_*640del
ENST00000697694.1:c.274_277del	ENSP00000513402.1:p.Tyr92IlefsTer29
ENST00000697695.1:n.1232_1235del
ENST00000337432.9:c.625_628del MANE Select	ENSP00000336701.4:p.Tyr209IlefsTer29
ENST00000337432.8:c.625_628del	ENSP00000336701.4:p.Tyr209IlefsTer29
ENST00000413590.5:c.263_266del
ENST00000425173.5:c.421_424del	ENSP00000407282.1:p.Tyr141IlefsTer?
ENST00000461271.5:c.274_277del	ENSP00000464056.1:p.Tyr92IlefsTer29
ENST00000475762.5:c.*1328_*1331del	ENSP00000432421.1:n.*1328_*1331del
ENST00000482007.5:c.*53_*56del	ENSP00000433332.1:n.*53_*56del
ENST00000487525.5:c.*53_*56del	ENSP00000431637.1:n.*53_*56del
ENST00000487921.5:n.537_540del
ENST00000583539.5:c.625_628del	ENSP00000463121.1:p.Tyr209IlefsTer29
ENST00000584617.5:c.347_350del
NM_058216.2:c.625_628del	NP_478123.1:p.Tyr209IlefsTer29
NR_103872.1:n.529_532del
XM_006722001.2:c.625_628del	XP_006722064.1:p.Tyr209IlefsTer29
XM_006722002.2:c.625_628del	XP_006722065.1:p.Tyr209IlefsTer29
XM_006722004.2:c.274_277del	XP_006722067.1:p.Tyr92IlefsTer29
XM_006722005.2:c.274_277del	XP_006722068.1:p.Tyr92IlefsTer29
XM_011525092.1:c.274_277del	XP_011523394.1:p.Tyr92IlefsTer29
XM_011525093.1:c.274_277del	XP_011523395.1:p.Tyr92IlefsTer29
XM_011525094.1:c.274_277del	XP_011523396.1:p.Tyr92IlefsTer29
XR_934513.1:n.698_701del
XR_934514.1:n.698_701del
XM_006722001.4:c.625_628del	XP_006722064.1:p.Tyr209IlefsTer29
XM_006722002.4:c.625_628del	XP_006722065.1:p.Tyr209IlefsTer29
XM_006722004.3:c.274_277del	XP_006722067.1:p.Tyr92IlefsTer29
XM_006722005.3:c.274_277del	XP_006722068.1:p.Tyr92IlefsTer29
XM_011525092.2:c.274_277del	XP_011523394.1:p.Tyr92IlefsTer29
XM_011525093.2:c.274_277del	XP_011523395.1:p.Tyr92IlefsTer29
XM_011525094.2:c.274_277del	XP_011523396.1:p.Tyr92IlefsTer29
XM_017024914.1:c.274_277del	XP_016880403.1:p.Tyr92IlefsTer29
XM_017024915.1:c.274_277del	XP_016880404.1:p.Tyr92IlefsTer29
XM_017024916.1:c.274_277del	XP_016880405.1:p.Tyr92IlefsTer29
XM_017024917.1:c.274_277del	XP_016880406.1:p.Tyr92IlefsTer29
XM_017024918.2:c.274_277del	XP_016880407.1:p.Tyr92IlefsTer29
XM_017024919.1:c.274_277del	XP_016880408.1:p.Tyr92IlefsTer29
XR_934513.3:n.1129_1132del
XR_934514.3:n.1129_1132del
NM_058216.3:c.625_628del MANE Select	NP_478123.1:p.Tyr209IlefsTer29
NR_103872.2:n.500_503del