Canonical Allele Identifier: CA2573054506

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 1177649
• ClinVar RCV Id: RCV001786499
• dbSNP Id: rs2143742992

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58696693_58696859del , CM000679.2:g.58696693_58696859del	GRCh38
NC_000017.10:g.56774054_56774220del , CM000679.1:g.56774054_56774220del	GRCh37
NC_000017.9:g.54129053_54129219del	NCBI36
NG_023199.1:g.9092_9258del , LRG_314:g.9092_9258del
NG_047169.1:g.222_388del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.54_220del
ENST00000697675.1:n.3002_3168del
ENST00000697676.1:n.465_631del
ENST00000697677.1:n.1486_1652del
ENST00000697678.1:n.307_473del
ENST00000697679.1:n.1479_1645del
ENST00000697680.1:c.*1269_*1435del
ENST00000697681.1:c.*1296_*1462del
ENST00000697683.1:c.*1269_*1435del
ENST00000697684.1:n.465_631del
ENST00000697685.1:c.*1268+1504_*1268+1670del	ENSP00000513396.1:n.*1268+1504_*1268+1670del
ENST00000697686.1:c.54_220del
ENST00000697687.1:n.450+1504_450+1670del
ENST00000697688.1:n.451_617del
ENST00000697689.1:c.*1107+1504_*1107+1670del	ENSP00000513398.1:n.*1107+1504_*1107+1670del
ENST00000697690.1:c.405_571del
ENST00000697691.1:c.*377_*543del
ENST00000697692.1:c.*417_*583del
ENST00000697694.1:c.54_220del
ENST00000697695.1:n.1012_1178del
ENST00000337432.9:c.405_571del
ENST00000337432.8:c.405_571del
ENST00000413590.5:c.43_209del
ENST00000425173.5:c.201_367del
ENST00000461271.5:c.54_220del
ENST00000475762.5:c.*1108_*1274del
ENST00000482007.5:c.404+1504_404+1670del	ENSP00000433332.1:n.404+1504_404+1670del
ENST00000487525.5:c.404+1504_404+1670del	ENSP00000431637.1:n.404+1504_404+1670del
ENST00000487921.5:n.317_483del
ENST00000583539.5:c.405_571del
ENST00000584617.5:c.127_293del
ENST00000622327.4:c.141_307del
NM_058216.2:c.405_571del
NR_103872.1:n.475+1504_475+1670del
XM_006722001.2:c.405_571del
XM_006722002.2:c.405_571del
XM_006722004.2:c.54_220del
XM_006722005.2:c.54_220del
XM_011525092.1:c.54_220del
XM_011525093.1:c.54_220del
XM_011525094.1:c.54_220del
XR_934513.1:n.478_644del
XR_934514.1:n.478_644del
XM_006722001.4:c.405_571del
XM_006722002.4:c.405_571del
XM_006722004.3:c.54_220del
XM_006722005.3:c.54_220del
XM_011525092.2:c.54_220del
XM_011525093.2:c.54_220del
XM_011525094.2:c.54_220del
XM_017024914.1:c.54_220del
XM_017024915.1:c.54_220del
XM_017024916.1:c.54_220del
XM_017024917.1:c.54_220del
XM_017024918.2:c.54_220del
XM_017024919.1:c.54_220del
XR_934513.3:n.909_1075del
XR_934514.3:n.909_1075del
NM_058216.3:c.405_571del
NR_103872.2:n.446+1504_446+1670del