Canonical Allele Identifier: CA1139665729

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 967734
• ClinVar RCV Id: RCV001242718
• dbSNP Id: rs1567794476

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703328del , CM000679.2:g.58703328del	GRCh38
NC_000017.10:g.56780689del , CM000679.1:g.56780689del	GRCh37
NC_000017.9:g.54135688del	NCBI36
NG_023199.1:g.15727del , LRG_314:g.15727del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.353del	ENSP00000464056.2:p.Lys118ArgfsTer4
ENST00000697677.1:n.1785del
ENST00000697678.1:n.606del
ENST00000697679.1:n.1778del
ENST00000697680.1:c.*1568del	ENSP00000513392.1:n.*1568del
ENST00000697681.1:c.*1720del	ENSP00000513393.1:n.*1720del
ENST00000697683.1:c.*1568del	ENSP00000513395.1:n.*1568del
ENST00000697684.1:n.764del
ENST00000697685.1:c.*1401del	ENSP00000513396.1:n.*1401del
ENST00000697686.1:c.353del	ENSP00000513397.1:p.Lys118ArgfsTer4
ENST00000697687.1:n.583del
ENST00000697688.1:n.750del
ENST00000697689.1:c.*1240del	ENSP00000513398.1:n.*1240del
ENST00000697690.1:c.704del	ENSP00000513399.1:p.Lys235ArgfsTer4
ENST00000697691.1:c.*676del	ENSP00000513400.1:n.*676del
ENST00000697692.1:c.*716del	ENSP00000513401.1:n.*716del
ENST00000697694.1:c.353del	ENSP00000513402.1:p.Lys118ArgfsTer4
ENST00000697695.1:n.1311del
ENST00000337432.9:c.704del MANE Select	ENSP00000336701.4:p.Lys235ArgfsTer4
ENST00000337432.8:c.704del	ENSP00000336701.4:p.Lys235ArgfsTer4
ENST00000413590.5:c.342del
ENST00000425173.5:c.500del	ENSP00000407282.1:p.Lys167ArgfsTer?
ENST00000461271.5:c.353del	ENSP00000464056.1:p.Lys118ArgfsTer4
ENST00000475762.5:c.*1407del	ENSP00000432421.1:n.*1407del
ENST00000482007.5:c.*132del	ENSP00000433332.1:n.*132del
ENST00000487525.5:c.*132del	ENSP00000431637.1:n.*132del
ENST00000487921.5:n.616del
ENST00000583539.5:c.704del	ENSP00000463121.1:p.Lys235ArgfsTer4
ENST00000584617.5:c.426del
NM_058216.2:c.704del	NP_478123.1:p.Lys235ArgfsTer4
NR_103872.1:n.608del
XM_006722001.2:c.704del	XP_006722064.1:p.Lys235ArgfsTer4
XM_006722002.2:c.704del	XP_006722065.1:p.Lys235ArgfsTer4
XM_006722004.2:c.353del	XP_006722067.1:p.Lys118ArgfsTer4
XM_006722005.2:c.353del	XP_006722068.1:p.Lys118ArgfsTer4
XM_011525092.1:c.353del	XP_011523394.1:p.Lys118ArgfsTer4
XM_011525093.1:c.353del	XP_011523395.1:p.Lys118ArgfsTer4
XM_011525094.1:c.353del	XP_011523396.1:p.Lys118ArgfsTer4
XR_934513.1:n.777del
XR_934514.1:n.777del
XM_006722001.4:c.704del	XP_006722064.1:p.Lys235ArgfsTer4
XM_006722002.4:c.704del	XP_006722065.1:p.Lys235ArgfsTer4
XM_006722004.3:c.353del	XP_006722067.1:p.Lys118ArgfsTer4
XM_006722005.3:c.353del	XP_006722068.1:p.Lys118ArgfsTer4
XM_011525092.2:c.353del	XP_011523394.1:p.Lys118ArgfsTer4
XM_011525093.2:c.353del	XP_011523395.1:p.Lys118ArgfsTer4
XM_011525094.2:c.353del	XP_011523396.1:p.Lys118ArgfsTer4
XM_017024914.1:c.353del	XP_016880403.1:p.Lys118ArgfsTer4
XM_017024915.1:c.353del	XP_016880404.1:p.Lys118ArgfsTer4
XM_017024916.1:c.353del	XP_016880405.1:p.Lys118ArgfsTer4
XM_017024917.1:c.353del	XP_016880406.1:p.Lys118ArgfsTer4
XM_017024918.2:c.353del	XP_016880407.1:p.Lys118ArgfsTer4
XM_017024919.1:c.353del	XP_016880408.1:p.Lys118ArgfsTer4
XR_934513.3:n.1208del
XR_934514.3:n.1208del
NM_058216.3:c.704del MANE Select	NP_478123.1:p.Lys235ArgfsTer4
NR_103872.2:n.579del