Canonical Allele Identifier: CA501075226

Gene: RAD51C

Linked Data

• dbSNP Id: rs2143799060
• MyVariant Identifiers: chr17:g.56780627T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703266T>A , CM000679.2:g.58703266T>A	GRCh38
NC_000017.10:g.56780627T>A , CM000679.1:g.56780627T>A	GRCh37
NC_000017.9:g.54135626T>A	NCBI36
NG_023199.1:g.15665T>A , LRG_314:g.15665T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.291T>A	ENSP00000464056.2:p.Arg97=
ENST00000697677.1:n.1723T>A
ENST00000697678.1:n.544T>A
ENST00000697679.1:n.1716T>A
ENST00000697680.1:c.*1506T>A	ENSP00000513392.1:n.*1506T>A
ENST00000697681.1:c.*1658T>A	ENSP00000513393.1:n.*1658T>A
ENST00000697683.1:c.*1506T>A	ENSP00000513395.1:n.*1506T>A
ENST00000697684.1:n.702T>A
ENST00000697685.1:c.*1339T>A	ENSP00000513396.1:n.*1339T>A
ENST00000697686.1:c.291T>A	ENSP00000513397.1:p.Arg97=
ENST00000697687.1:n.521T>A
ENST00000697688.1:n.688T>A
ENST00000697689.1:c.*1178T>A	ENSP00000513398.1:n.*1178T>A
ENST00000697690.1:c.642T>A	ENSP00000513399.1:p.Arg214=
ENST00000697691.1:c.*614T>A	ENSP00000513400.1:n.*614T>A
ENST00000697692.1:c.*654T>A	ENSP00000513401.1:n.*654T>A
ENST00000697694.1:c.291T>A	ENSP00000513402.1:p.Arg97=
ENST00000697695.1:n.1249T>A
ENST00000337432.9:c.642T>A MANE Select	ENSP00000336701.4:p.Arg214=
ENST00000337432.8:c.642T>A	ENSP00000336701.4:p.Arg214=
ENST00000413590.5:c.280T>A
ENST00000425173.5:c.438T>A	ENSP00000407282.1:p.Arg146=
ENST00000461271.5:c.291T>A	ENSP00000464056.1:p.Arg97=
ENST00000475762.5:c.*1345T>A	ENSP00000432421.1:n.*1345T>A
ENST00000482007.5:c.*70T>A	ENSP00000433332.1:n.*70T>A
ENST00000487525.5:c.*70T>A	ENSP00000431637.1:n.*70T>A
ENST00000487921.5:n.554T>A
ENST00000583539.5:c.642T>A	ENSP00000463121.1:p.Arg214=
ENST00000584617.5:c.364T>A
NM_058216.2:c.642T>A	NP_478123.1:p.Arg214=
NR_103872.1:n.546T>A
XM_006722001.2:c.642T>A	XP_006722064.1:p.Arg214=
XM_006722002.2:c.642T>A	XP_006722065.1:p.Arg214=
XM_006722004.2:c.291T>A	XP_006722067.1:p.Arg97=
XM_006722005.2:c.291T>A	XP_006722068.1:p.Arg97=
XM_011525092.1:c.291T>A	XP_011523394.1:p.Arg97=
XM_011525093.1:c.291T>A	XP_011523395.1:p.Arg97=
XM_011525094.1:c.291T>A	XP_011523396.1:p.Arg97=
XR_934513.1:n.715T>A
XR_934514.1:n.715T>A
XM_006722001.4:c.642T>A	XP_006722064.1:p.Arg214=
XM_006722002.4:c.642T>A	XP_006722065.1:p.Arg214=
XM_006722004.3:c.291T>A	XP_006722067.1:p.Arg97=
XM_006722005.3:c.291T>A	XP_006722068.1:p.Arg97=
XM_011525092.2:c.291T>A	XP_011523394.1:p.Arg97=
XM_011525093.2:c.291T>A	XP_011523395.1:p.Arg97=
XM_011525094.2:c.291T>A	XP_011523396.1:p.Arg97=
XM_017024914.1:c.291T>A	XP_016880403.1:p.Arg97=
XM_017024915.1:c.291T>A	XP_016880404.1:p.Arg97=
XM_017024916.1:c.291T>A	XP_016880405.1:p.Arg97=
XM_017024917.1:c.291T>A	XP_016880406.1:p.Arg97=
XM_017024918.2:c.291T>A	XP_016880407.1:p.Arg97=
XM_017024919.1:c.291T>A	XP_016880408.1:p.Arg97=
XR_934513.3:n.1146T>A
XR_934514.3:n.1146T>A
NM_058216.3:c.642T>A MANE Select	NP_478123.1:p.Arg214=
NR_103872.2:n.517T>A