Canonical Allele Identifier: CA658658644

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 480503
• ClinVar RCV Id: RCV000573708 ; RCV001345061
• dbSNP Id: rs1555597217
• MyVariant Identifiers: chr17:g.56780662_56780664del (hg19) ; chr17:g.58703301_58703303del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703301_58703303del , CM000679.2:g.58703301_58703303del	GRCh38
NC_000017.10:g.56780662_56780664del , CM000679.1:g.56780662_56780664del	GRCh37
NC_000017.9:g.54135661_54135663del	NCBI36
NG_023199.1:g.15700_15702del , LRG_314:g.15700_15702del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.326_328del	ENSP00000464056.2:p.Leu109del
ENST00000697677.1:n.1758_1760del
ENST00000697678.1:n.579_581del
ENST00000697679.1:n.1751_1753del
ENST00000697680.1:c.*1541_*1543del	ENSP00000513392.1:n.*1541_*1543del
ENST00000697681.1:c.*1693_*1695del	ENSP00000513393.1:n.*1693_*1695del
ENST00000697683.1:c.*1541_*1543del	ENSP00000513395.1:n.*1541_*1543del
ENST00000697684.1:n.737_739del
ENST00000697685.1:c.*1374_*1376del	ENSP00000513396.1:n.*1374_*1376del
ENST00000697686.1:c.326_328del	ENSP00000513397.1:p.Leu109del
ENST00000697687.1:n.556_558del
ENST00000697688.1:n.723_725del
ENST00000697689.1:c.*1213_*1215del	ENSP00000513398.1:n.*1213_*1215del
ENST00000697690.1:c.677_679del	ENSP00000513399.1:p.Leu226del
ENST00000697691.1:c.*649_*651del	ENSP00000513400.1:n.*649_*651del
ENST00000697692.1:c.*689_*691del	ENSP00000513401.1:n.*689_*691del
ENST00000697694.1:c.326_328del	ENSP00000513402.1:p.Leu109del
ENST00000697695.1:n.1284_1286del
ENST00000337432.9:c.677_679del MANE Select	ENSP00000336701.4:p.Leu226del
ENST00000337432.8:c.677_679del	ENSP00000336701.4:p.Leu226del
ENST00000413590.5:c.315_317del
ENST00000425173.5:c.473_475del	ENSP00000407282.1:p.Leu158del
ENST00000461271.5:c.326_328del	ENSP00000464056.1:p.Leu109del
ENST00000475762.5:c.*1380_*1382del	ENSP00000432421.1:n.*1380_*1382del
ENST00000482007.5:c.*105_*107del	ENSP00000433332.1:n.*105_*107del
ENST00000487525.5:c.*105_*107del	ENSP00000431637.1:n.*105_*107del
ENST00000487921.5:n.589_591del
ENST00000583539.5:c.677_679del	ENSP00000463121.1:p.Leu226del
ENST00000584617.5:c.399_401del
NM_058216.2:c.677_679del	NP_478123.1:p.Leu226del
NR_103872.1:n.581_583del
XM_006722001.2:c.677_679del	XP_006722064.1:p.Leu226del
XM_006722002.2:c.677_679del	XP_006722065.1:p.Leu226del
XM_006722004.2:c.326_328del	XP_006722067.1:p.Leu109del
XM_006722005.2:c.326_328del	XP_006722068.1:p.Leu109del
XM_011525092.1:c.326_328del	XP_011523394.1:p.Leu109del
XM_011525093.1:c.326_328del	XP_011523395.1:p.Leu109del
XM_011525094.1:c.326_328del	XP_011523396.1:p.Leu109del
XR_934513.1:n.750_752del
XR_934514.1:n.750_752del
XM_006722001.4:c.677_679del	XP_006722064.1:p.Leu226del
XM_006722002.4:c.677_679del	XP_006722065.1:p.Leu226del
XM_006722004.3:c.326_328del	XP_006722067.1:p.Leu109del
XM_006722005.3:c.326_328del	XP_006722068.1:p.Leu109del
XM_011525092.2:c.326_328del	XP_011523394.1:p.Leu109del
XM_011525093.2:c.326_328del	XP_011523395.1:p.Leu109del
XM_011525094.2:c.326_328del	XP_011523396.1:p.Leu109del
XM_017024914.1:c.326_328del	XP_016880403.1:p.Leu109del
XM_017024915.1:c.326_328del	XP_016880404.1:p.Leu109del
XM_017024916.1:c.326_328del	XP_016880405.1:p.Leu109del
XM_017024917.1:c.326_328del	XP_016880406.1:p.Leu109del
XM_017024918.2:c.326_328del	XP_016880407.1:p.Leu109del
XM_017024919.1:c.326_328del	XP_016880408.1:p.Leu109del
XR_934513.3:n.1181_1183del
XR_934514.3:n.1181_1183del
NM_058216.3:c.677_679del MANE Select	NP_478123.1:p.Leu226del
NR_103872.2:n.552_554del