Canonical Allele Identifier: CA2573054502

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 1177655
• ClinVar RCV Id: RCV001786505

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58709861_58709992del , CM000679.2:g.58709861_58709992del	GRCh38
NC_000017.10:g.56787222_56787353del , CM000679.1:g.56787222_56787353del	GRCh37
NC_000017.9:g.54142221_54142352del	NCBI36
NG_023199.1:g.22260_22391del , LRG_314:g.22260_22391del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.357_486+2del
ENST00000697678.1:n.610_739+2del
ENST00000697679.1:n.1782_1911+2del
ENST00000697680.1:c.*1572_*1701+2del
ENST00000697681.1:c.*1869_*1998+2del
ENST00000697683.1:c.*1572_*1701+2del
ENST00000697684.1:n.768_897+2del
ENST00000697685.1:c.*1405_*1534+2del
ENST00000697686.1:c.357_486+2del
ENST00000697687.1:n.587_716+2del
ENST00000697688.1:n.754_883+2del
ENST00000697689.1:c.*1244_*1373+2del
ENST00000697690.1:c.708_837+2del
ENST00000697691.1:c.*680_*809+2del
ENST00000697692.1:c.*720_*849+2del
ENST00000697694.1:c.357_486+2del
ENST00000697695.1:n.1315_1444+2del
ENST00000337432.9:c.708_837+2del
ENST00000337432.8:c.708_837+2del
ENST00000413590.5:c.346_475+2del
ENST00000475762.5:c.*1411_*1540+2del
ENST00000482007.5:c.*136_*265+2del
ENST00000487525.5:c.*281_*410+2del
ENST00000578151.1:n.43_172+2del
ENST00000581221.5:n.223_352+2del
ENST00000583539.5:c.708_837+2del
ENST00000584617.5:c.430_559+2del
ENST00000584804.1:c.3_132+2del
NM_058216.2:c.708_837+2del
NR_103872.1:n.612_741+2del
XM_006722001.2:c.708_837+2del
XM_006722002.2:c.708_837+2del
XM_006722004.2:c.357_486+2del
XM_006722005.2:c.357_486+2del
XM_011525092.1:c.357_486+2del
XM_011525093.1:c.357_486+2del
XM_011525094.1:c.357_486+2del
XR_934513.1:n.926_1055+2del
XR_934514.1:n.926_1055+2del
XM_006722001.4:c.708_837+2del
XM_006722002.4:c.708_837+2del
XM_006722004.3:c.357_486+2del
XM_006722005.3:c.357_486+2del
XM_011525092.2:c.357_486+2del
XM_011525093.2:c.357_486+2del
XM_011525094.2:c.357_486+2del
XM_017024914.1:c.357_486+2del
XM_017024915.1:c.357_486+2del
XM_017024916.1:c.357_486+2del
XM_017024917.1:c.357_486+2del
XM_017024918.2:c.357_486+2del
XM_017024919.1:c.357_486+2del
XR_934513.3:n.1357_1486+2del
XR_934514.3:n.1357_1486+2del
NM_058216.3:c.708_837+2del
NR_103872.2:n.583_712+2del