Canonical Allele Identifier: CA2580094306

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 1801656
• ClinVar RCV Id: RCV003164692 ; RCV003464564

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58724101del , CM000679.2:g.58724101del	GRCh38
NC_000017.10:g.56801462del , CM000679.1:g.56801462del	GRCh37
NC_000017.9:g.54156461del	NCBI36
NG_023199.1:g.36500del , LRG_314:g.36500del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.614+1del
ENST00000697680.1:c.*1929+1del
ENST00000697681.1:c.*2126+1del
ENST00000697683.1:c.*1829+1del
ENST00000697684.1:n.1025+1del
ENST00000697685.1:c.*1662+1del
ENST00000697686.1:c.614+1del
ENST00000697687.1:n.845del
ENST00000697688.1:n.1012del
ENST00000697689.1:c.*1440+3289del	ENSP00000513398.1:n.*1440+3289del
ENST00000697690.1:c.904+3289del	ENSP00000513399.1:n.904+3289del
ENST00000697691.1:c.*937+1del
ENST00000697692.1:c.*977+1del
ENST00000697694.1:c.614+1del
ENST00000697695.1:n.1572+1del
ENST00000337432.9:c.965+1del
ENST00000337432.8:c.965+1del
ENST00000413590.5:c.603+1del
ENST00000475762.5:c.*1601+1del
ENST00000482007.5:c.*393+1del
ENST00000487525.5:c.*538+1del
ENST00000578151.1:n.239+3289del
ENST00000581221.5:n.480+1del
ENST00000583539.5:c.965+1del
ENST00000584617.5:c.687+1del
ENST00000584804.1:c.199+3289del	ENSP00000463658.1:n.199+3289del
NM_058216.2:c.965+1del
NR_103872.1:n.869+1del
XM_006722001.2:c.965+1del
XM_006722002.2:c.904+3289del	XP_006722065.1:n.904+3289del
XM_006722004.2:c.614+1del
XM_006722005.2:c.614+1del
XM_011525092.1:c.614+1del
XM_011525093.1:c.614+1del
XM_011525094.1:c.614+1del
XR_934513.1:n.1183+1del
XR_934514.1:n.1183+1del
XM_006722001.4:c.965+1del
XM_006722002.4:c.904+3289del	XP_006722065.1:n.904+3289del
XM_006722004.3:c.614+1del
XM_006722005.3:c.614+1del
XM_011525092.2:c.614+1del
XM_011525093.2:c.614+1del
XM_011525094.2:c.614+1del
XM_017024914.1:c.614+1del
XM_017024915.1:c.614+1del
XM_017024916.1:c.614+1del
XM_017024917.1:c.614+1del
XM_017024918.2:c.614+1del
XM_017024919.1:c.553+3289del	XP_016880408.1:n.553+3289del
XR_934513.3:n.1614+1del
XR_934514.3:n.1614+1del
NM_058216.3:c.965+1del
NR_103872.2:n.840+1del