Canonical Allele Identifier: CA2580613171

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 2021697
• ClinVar RCV Id: RCV002847217 ; RCV003465851

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703239_58703242del , CM000679.2:g.58703239_58703242del	GRCh38
NC_000017.10:g.56780600_56780603del , CM000679.1:g.56780600_56780603del	GRCh37
NC_000017.9:g.54135599_54135602del	NCBI36
NG_023199.1:g.15638_15641del , LRG_314:g.15638_15641del

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.264_267del	ENSP00000464056.2:p.Ser89IlefsTer?
ENST00000697677.1:n.1696_1699del
ENST00000697678.1:n.517_520del
ENST00000697679.1:n.1689_1692del
ENST00000697680.1:c.*1479_*1482del	ENSP00000513392.1:n.*1479_*1482del
ENST00000697681.1:c.*1631_*1634del	ENSP00000513393.1:n.*1631_*1634del
ENST00000697683.1:c.*1479_*1482del	ENSP00000513395.1:n.*1479_*1482del
ENST00000697684.1:n.675_678del
ENST00000697685.1:c.*1312_*1315del	ENSP00000513396.1:n.*1312_*1315del
ENST00000697686.1:c.264_267del	ENSP00000513397.1:p.Ser89IlefsTer?
ENST00000697687.1:n.494_497del
ENST00000697688.1:n.661_664del
ENST00000697689.1:c.*1151_*1154del	ENSP00000513398.1:n.*1151_*1154del
ENST00000697690.1:c.615_618del	ENSP00000513399.1:p.Ser206IlefsTer?
ENST00000697691.1:c.*587_*590del	ENSP00000513400.1:n.*587_*590del
ENST00000697692.1:c.*627_*630del	ENSP00000513401.1:n.*627_*630del
ENST00000697694.1:c.264_267del	ENSP00000513402.1:p.Ser89IlefsTer?
ENST00000697695.1:n.1222_1225del
ENST00000337432.9:c.615_618del MANE Select	ENSP00000336701.4:p.Ser206IlefsTer?
ENST00000337432.8:c.615_618del	ENSP00000336701.4:p.Ser206IlefsTer?
ENST00000413590.5:c.253_256del
ENST00000425173.5:c.411_414del	ENSP00000407282.1:p.Ser138IlefsTer?
ENST00000461271.5:c.264_267del	ENSP00000464056.1:p.Ser89IlefsTer?
ENST00000475762.5:c.*1318_*1321del	ENSP00000432421.1:n.*1318_*1321del
ENST00000482007.5:c.*43_*46del	ENSP00000433332.1:n.*43_*46del
ENST00000487525.5:c.*43_*46del	ENSP00000431637.1:n.*43_*46del
ENST00000487921.5:n.527_530del
ENST00000583539.5:c.615_618del	ENSP00000463121.1:p.Ser206IlefsTer?
ENST00000584617.5:c.337_340del
NM_058216.2:c.615_618del	NP_478123.1:p.Ser206IlefsTer?
NR_103872.1:n.519_522del
XM_006722001.2:c.615_618del	XP_006722064.1:p.Ser206IlefsTer?
XM_006722002.2:c.615_618del	XP_006722065.1:p.Ser206IlefsTer?
XM_006722004.2:c.264_267del	XP_006722067.1:p.Ser89IlefsTer?
XM_006722005.2:c.264_267del	XP_006722068.1:p.Ser89IlefsTer?
XM_011525092.1:c.264_267del	XP_011523394.1:p.Ser89IlefsTer?
XM_011525093.1:c.264_267del	XP_011523395.1:p.Ser89IlefsTer?
XM_011525094.1:c.264_267del	XP_011523396.1:p.Ser89IlefsTer?
XR_934513.1:n.688_691del
XR_934514.1:n.688_691del
XM_006722001.4:c.615_618del	XP_006722064.1:p.Ser206IlefsTer?
XM_006722002.4:c.615_618del	XP_006722065.1:p.Ser206IlefsTer?
XM_006722004.3:c.264_267del	XP_006722067.1:p.Ser89IlefsTer?
XM_006722005.3:c.264_267del	XP_006722068.1:p.Ser89IlefsTer?
XM_011525092.2:c.264_267del	XP_011523394.1:p.Ser89IlefsTer?
XM_011525093.2:c.264_267del	XP_011523395.1:p.Ser89IlefsTer?
XM_011525094.2:c.264_267del	XP_011523396.1:p.Ser89IlefsTer?
XM_017024914.1:c.264_267del	XP_016880403.1:p.Ser89IlefsTer?
XM_017024915.1:c.264_267del	XP_016880404.1:p.Ser89IlefsTer?
XM_017024916.1:c.264_267del	XP_016880405.1:p.Ser89IlefsTer?
XM_017024917.1:c.264_267del	XP_016880406.1:p.Ser89IlefsTer?
XM_017024918.2:c.264_267del	XP_016880407.1:p.Ser89IlefsTer?
XM_017024919.1:c.264_267del	XP_016880408.1:p.Ser89IlefsTer?
XR_934513.3:n.1119_1122del
XR_934514.3:n.1119_1122del
NM_058216.3:c.615_618del MANE Select	NP_478123.1:p.Ser206IlefsTer?
NR_103872.2:n.490_493del