Canonical Allele Identifier: CA2695200294

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 2663993
• ClinVar RCV Id: RCV003444455

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58701342_58706141del , CM000679.2:g.58701342_58706141del	GRCh38
NC_000017.10:g.56778703_56783502del , CM000679.1:g.56778703_56783502del	GRCh37
NC_000017.9:g.54133702_54138501del	NCBI36
NG_023199.1:g.13741_18540del , LRG_314:g.13741_18540del

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.221-1854_354+2812del
ENST00000697678.1:n.474-1854_607+2812del
ENST00000697679.1:n.1646-1854_1779+2812del
ENST00000697680.1:c.*1436-1854_*1569+2812del
ENST00000697681.1:c.*1587+1343_*1866+119del
ENST00000697683.1:c.*1436-1854_*1569+2812del
ENST00000697684.1:n.632-1854_765+2812del
ENST00000697685.1:c.*1269-1854_*1402+2812del
ENST00000697686.1:c.221-1854_354+2812del
ENST00000697687.1:n.451-1854_584+2812del
ENST00000697688.1:n.618-1854_751+2812del
ENST00000697689.1:c.*1108-1854_*1241+2812del
ENST00000697690.1:c.572-1854_705+2812del
ENST00000697691.1:c.*544-1854_*677+2812del
ENST00000697692.1:c.*584-1854_*717+2812del
ENST00000697694.1:c.221-1854_354+2812del
ENST00000697695.1:n.1179-1854_1312+2812del
ENST00000337432.9:c.572-1854_705+2812del
ENST00000337432.8:c.572-1854_705+2812del
ENST00000413590.5:c.210-1854_343+2812del
ENST00000425173.5:c.368-1854_502-348del
ENST00000461271.5:c.221-1854_354+2812del
ENST00000475762.5:c.*1275-1854_*1408+2812del
ENST00000482007.5:c.405-1854_*133+2812del
ENST00000487525.5:c.405-1854_*278+119del
ENST00000583539.5:c.572-1854_705+2812del
ENST00000584617.5:c.294-1854_427+2812del
NM_058216.2:c.572-1854_705+2812del
NR_103872.1:n.476-1854_609+2812del
XM_006722001.2:c.572-1854_705+2812del
XM_006722002.2:c.572-1854_705+2812del
XM_006722004.2:c.221-1854_354+2812del
XM_006722005.2:c.221-1854_354+2812del
XM_011525092.1:c.221-1854_354+2812del
XM_011525093.1:c.221-1854_354+2812del
XM_011525094.1:c.221-1854_354+2812del
XR_934513.1:n.645-1854_923+119del
XR_934514.1:n.645-1854_923+119del
XM_006722001.4:c.572-1854_705+2812del
XM_006722002.4:c.572-1854_705+2812del
XM_006722004.3:c.221-1854_354+2812del
XM_006722005.3:c.221-1854_354+2812del
XM_011525092.2:c.221-1854_354+2812del
XM_011525093.2:c.221-1854_354+2812del
XM_011525094.2:c.221-1854_354+2812del
XM_017024914.1:c.221-1854_354+2812del
XM_017024915.1:c.221-1854_354+2812del
XM_017024916.1:c.221-1854_354+2812del
XM_017024917.1:c.221-1854_354+2812del
XM_017024918.2:c.221-1854_354+2812del
XM_017024919.1:c.221-1854_354+2812del
XR_934513.3:n.1076-1854_1354+119del
XR_934514.3:n.1076-1854_1354+119del
NM_058216.3:c.572-1854_705+2812del
NR_103872.2:n.447-1854_580+2812del