Canonical Allele Identifier: CA1139665728

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 952558
• ClinVar RCV Id: RCV001224684
• dbSNP Id: rs2048269550

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703221_58703227del , CM000679.2:g.58703221_58703227del	GRCh38
NC_000017.10:g.56780582_56780588del , CM000679.1:g.56780582_56780588del	GRCh37
NC_000017.9:g.54135581_54135587del	NCBI36
NG_023199.1:g.15620_15626del , LRG_314:g.15620_15626del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.246_252del	ENSP00000464056.2:p.Phe82LeufsTer?
ENST00000697677.1:n.1678_1684del
ENST00000697678.1:n.499_505del
ENST00000697679.1:n.1671_1677del
ENST00000697680.1:c.*1461_*1467del	ENSP00000513392.1:n.*1461_*1467del
ENST00000697681.1:c.*1613_*1619del	ENSP00000513393.1:n.*1613_*1619del
ENST00000697683.1:c.*1461_*1467del	ENSP00000513395.1:n.*1461_*1467del
ENST00000697684.1:n.657_663del
ENST00000697685.1:c.*1294_*1300del	ENSP00000513396.1:n.*1294_*1300del
ENST00000697686.1:c.246_252del	ENSP00000513397.1:p.Phe82LeufsTer?
ENST00000697687.1:n.476_482del
ENST00000697688.1:n.643_649del
ENST00000697689.1:c.*1133_*1139del	ENSP00000513398.1:n.*1133_*1139del
ENST00000697690.1:c.597_603del	ENSP00000513399.1:p.Phe199LeufsTer?
ENST00000697691.1:c.*569_*575del	ENSP00000513400.1:n.*569_*575del
ENST00000697692.1:c.*609_*615del	ENSP00000513401.1:n.*609_*615del
ENST00000697694.1:c.246_252del	ENSP00000513402.1:p.Phe82LeufsTer?
ENST00000697695.1:n.1204_1210del
ENST00000337432.9:c.597_603del MANE Select	ENSP00000336701.4:p.Phe199LeufsTer?
ENST00000337432.8:c.597_603del	ENSP00000336701.4:p.Phe199LeufsTer?
ENST00000413590.5:c.235_241del
ENST00000425173.5:c.393_399del	ENSP00000407282.1:p.Phe131LeufsTer?
ENST00000461271.5:c.246_252del	ENSP00000464056.1:p.Phe82LeufsTer?
ENST00000475762.5:c.*1300_*1306del	ENSP00000432421.1:n.*1300_*1306del
ENST00000482007.5:c.*25_*31del	ENSP00000433332.1:n.*25_*31del
ENST00000487525.5:c.*25_*31del	ENSP00000431637.1:n.*25_*31del
ENST00000487921.5:n.509_515del
ENST00000583539.5:c.597_603del	ENSP00000463121.1:p.Phe199LeufsTer?
ENST00000584617.5:c.319_325del
NM_058216.2:c.597_603del	NP_478123.1:p.Phe199LeufsTer?
NR_103872.1:n.501_507del
XM_006722001.2:c.597_603del	XP_006722064.1:p.Phe199LeufsTer?
XM_006722002.2:c.597_603del	XP_006722065.1:p.Phe199LeufsTer?
XM_006722004.2:c.246_252del	XP_006722067.1:p.Phe82LeufsTer?
XM_006722005.2:c.246_252del	XP_006722068.1:p.Phe82LeufsTer?
XM_011525092.1:c.246_252del	XP_011523394.1:p.Phe82LeufsTer?
XM_011525093.1:c.246_252del	XP_011523395.1:p.Phe82LeufsTer?
XM_011525094.1:c.246_252del	XP_011523396.1:p.Phe82LeufsTer?
XR_934513.1:n.670_676del
XR_934514.1:n.670_676del
XM_006722001.4:c.597_603del	XP_006722064.1:p.Phe199LeufsTer?
XM_006722002.4:c.597_603del	XP_006722065.1:p.Phe199LeufsTer?
XM_006722004.3:c.246_252del	XP_006722067.1:p.Phe82LeufsTer?
XM_006722005.3:c.246_252del	XP_006722068.1:p.Phe82LeufsTer?
XM_011525092.2:c.246_252del	XP_011523394.1:p.Phe82LeufsTer?
XM_011525093.2:c.246_252del	XP_011523395.1:p.Phe82LeufsTer?
XM_011525094.2:c.246_252del	XP_011523396.1:p.Phe82LeufsTer?
XM_017024914.1:c.246_252del	XP_016880403.1:p.Phe82LeufsTer?
XM_017024915.1:c.246_252del	XP_016880404.1:p.Phe82LeufsTer?
XM_017024916.1:c.246_252del	XP_016880405.1:p.Phe82LeufsTer?
XM_017024917.1:c.246_252del	XP_016880406.1:p.Phe82LeufsTer?
XM_017024918.2:c.246_252del	XP_016880407.1:p.Phe82LeufsTer?
XM_017024919.1:c.246_252del	XP_016880408.1:p.Phe82LeufsTer?
XR_934513.3:n.1101_1107del
XR_934514.3:n.1101_1107del
NM_058216.3:c.597_603del MANE Select	NP_478123.1:p.Phe199LeufsTer?
NR_103872.2:n.472_478del