Canonical Allele Identifier: CA2825002568

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 3148640
• ClinVar RCV Id: RCV004442534

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703322del , CM000679.2:g.58703322del	GRCh38
NC_000017.10:g.56780683del , CM000679.1:g.56780683del	GRCh37
NC_000017.9:g.54135682del	NCBI36
NG_023199.1:g.15721del , LRG_314:g.15721del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.347del	ENSP00000464056.2:p.His116ProfsTer6
ENST00000697677.1:n.1779del
ENST00000697678.1:n.600del
ENST00000697679.1:n.1772del
ENST00000697680.1:c.*1562del	ENSP00000513392.1:n.*1562del
ENST00000697681.1:c.*1714del	ENSP00000513393.1:n.*1714del
ENST00000697683.1:c.*1562del	ENSP00000513395.1:n.*1562del
ENST00000697684.1:n.758del
ENST00000697685.1:c.*1395del	ENSP00000513396.1:n.*1395del
ENST00000697686.1:c.347del	ENSP00000513397.1:p.His116ProfsTer6
ENST00000697687.1:n.577del
ENST00000697688.1:n.744del
ENST00000697689.1:c.*1234del	ENSP00000513398.1:n.*1234del
ENST00000697690.1:c.698del	ENSP00000513399.1:p.His233ProfsTer6
ENST00000697691.1:c.*670del	ENSP00000513400.1:n.*670del
ENST00000697692.1:c.*710del	ENSP00000513401.1:n.*710del
ENST00000697694.1:c.347del	ENSP00000513402.1:p.His116ProfsTer6
ENST00000697695.1:n.1305del
ENST00000337432.9:c.698del MANE Select	ENSP00000336701.4:p.His233ProfsTer6
ENST00000337432.8:c.698del	ENSP00000336701.4:p.His233ProfsTer6
ENST00000413590.5:c.336del
ENST00000425173.5:c.494del	ENSP00000407282.1:p.His165ProfsTer?
ENST00000461271.5:c.347del	ENSP00000464056.1:p.His116ProfsTer6
ENST00000475762.5:c.*1401del	ENSP00000432421.1:n.*1401del
ENST00000482007.5:c.*126del	ENSP00000433332.1:n.*126del
ENST00000487525.5:c.*126del	ENSP00000431637.1:n.*126del
ENST00000487921.5:n.610del
ENST00000583539.5:c.698del	ENSP00000463121.1:p.His233ProfsTer6
ENST00000584617.5:c.420del
NM_058216.2:c.698del	NP_478123.1:p.His233ProfsTer6
NR_103872.1:n.602del
XM_006722001.2:c.698del	XP_006722064.1:p.His233ProfsTer6
XM_006722002.2:c.698del	XP_006722065.1:p.His233ProfsTer6
XM_006722004.2:c.347del	XP_006722067.1:p.His116ProfsTer6
XM_006722005.2:c.347del	XP_006722068.1:p.His116ProfsTer6
XM_011525092.1:c.347del	XP_011523394.1:p.His116ProfsTer6
XM_011525093.1:c.347del	XP_011523395.1:p.His116ProfsTer6
XM_011525094.1:c.347del	XP_011523396.1:p.His116ProfsTer6
XR_934513.1:n.771del
XR_934514.1:n.771del
XM_006722001.4:c.698del	XP_006722064.1:p.His233ProfsTer6
XM_006722002.4:c.698del	XP_006722065.1:p.His233ProfsTer6
XM_006722004.3:c.347del	XP_006722067.1:p.His116ProfsTer6
XM_006722005.3:c.347del	XP_006722068.1:p.His116ProfsTer6
XM_011525092.2:c.347del	XP_011523394.1:p.His116ProfsTer6
XM_011525093.2:c.347del	XP_011523395.1:p.His116ProfsTer6
XM_011525094.2:c.347del	XP_011523396.1:p.His116ProfsTer6
XM_017024914.1:c.347del	XP_016880403.1:p.His116ProfsTer6
XM_017024915.1:c.347del	XP_016880404.1:p.His116ProfsTer6
XM_017024916.1:c.347del	XP_016880405.1:p.His116ProfsTer6
XM_017024917.1:c.347del	XP_016880406.1:p.His116ProfsTer6
XM_017024918.2:c.347del	XP_016880407.1:p.His116ProfsTer6
XM_017024919.1:c.347del	XP_016880408.1:p.His116ProfsTer6
XR_934513.3:n.1202del
XR_934514.3:n.1202del
NM_058216.3:c.698del MANE Select	NP_478123.1:p.His233ProfsTer6
NR_103872.2:n.573del