Canonical Allele Identifier: CA2499224761

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 1072935
• ClinVar RCV Id: RCV003463007 ; RCV001385785
• dbSNP Id: rs2143797889

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703236del , CM000679.2:g.58703236del	GRCh38
NC_000017.10:g.56780597del , CM000679.1:g.56780597del	GRCh37
NC_000017.9:g.54135596del	NCBI36
NG_023199.1:g.15635del , LRG_314:g.15635del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.261del	ENSP00000464056.2:p.Leu88PhefsTer?
ENST00000697677.1:n.1693del
ENST00000697678.1:n.514del
ENST00000697679.1:n.1686del
ENST00000697680.1:c.*1476del	ENSP00000513392.1:n.*1476del
ENST00000697681.1:c.*1628del	ENSP00000513393.1:n.*1628del
ENST00000697683.1:c.*1476del	ENSP00000513395.1:n.*1476del
ENST00000697684.1:n.672del
ENST00000697685.1:c.*1309del	ENSP00000513396.1:n.*1309del
ENST00000697686.1:c.261del	ENSP00000513397.1:p.Leu88PhefsTer?
ENST00000697687.1:n.491del
ENST00000697688.1:n.658del
ENST00000697689.1:c.*1148del	ENSP00000513398.1:n.*1148del
ENST00000697690.1:c.612del	ENSP00000513399.1:p.Leu205PhefsTer?
ENST00000697691.1:c.*584del	ENSP00000513400.1:n.*584del
ENST00000697692.1:c.*624del	ENSP00000513401.1:n.*624del
ENST00000697694.1:c.261del	ENSP00000513402.1:p.Leu88PhefsTer?
ENST00000697695.1:n.1219del
ENST00000337432.9:c.612del MANE Select	ENSP00000336701.4:p.Leu205PhefsTer?
ENST00000337432.8:c.612del	ENSP00000336701.4:p.Leu205PhefsTer?
ENST00000413590.5:c.250del
ENST00000425173.5:c.408del	ENSP00000407282.1:p.Leu137PhefsTer?
ENST00000461271.5:c.261del	ENSP00000464056.1:p.Leu88PhefsTer?
ENST00000475762.5:c.*1315del	ENSP00000432421.1:n.*1315del
ENST00000482007.5:c.*40del	ENSP00000433332.1:n.*40del
ENST00000487525.5:c.*40del	ENSP00000431637.1:n.*40del
ENST00000487921.5:n.524del
ENST00000583539.5:c.612del	ENSP00000463121.1:p.Leu205PhefsTer?
ENST00000584617.5:c.334del
NM_058216.2:c.612del	NP_478123.1:p.Leu205PhefsTer?
NR_103872.1:n.516del
XM_006722001.2:c.612del	XP_006722064.1:p.Leu205PhefsTer?
XM_006722002.2:c.612del	XP_006722065.1:p.Leu205PhefsTer?
XM_006722004.2:c.261del	XP_006722067.1:p.Leu88PhefsTer?
XM_006722005.2:c.261del	XP_006722068.1:p.Leu88PhefsTer?
XM_011525092.1:c.261del	XP_011523394.1:p.Leu88PhefsTer?
XM_011525093.1:c.261del	XP_011523395.1:p.Leu88PhefsTer?
XM_011525094.1:c.261del	XP_011523396.1:p.Leu88PhefsTer?
XR_934513.1:n.685del
XR_934514.1:n.685del
XM_006722001.4:c.612del	XP_006722064.1:p.Leu205PhefsTer?
XM_006722002.4:c.612del	XP_006722065.1:p.Leu205PhefsTer?
XM_006722004.3:c.261del	XP_006722067.1:p.Leu88PhefsTer?
XM_006722005.3:c.261del	XP_006722068.1:p.Leu88PhefsTer?
XM_011525092.2:c.261del	XP_011523394.1:p.Leu88PhefsTer?
XM_011525093.2:c.261del	XP_011523395.1:p.Leu88PhefsTer?
XM_011525094.2:c.261del	XP_011523396.1:p.Leu88PhefsTer?
XM_017024914.1:c.261del	XP_016880403.1:p.Leu88PhefsTer?
XM_017024915.1:c.261del	XP_016880404.1:p.Leu88PhefsTer?
XM_017024916.1:c.261del	XP_016880405.1:p.Leu88PhefsTer?
XM_017024917.1:c.261del	XP_016880406.1:p.Leu88PhefsTer?
XM_017024918.2:c.261del	XP_016880407.1:p.Leu88PhefsTer?
XM_017024919.1:c.261del	XP_016880408.1:p.Leu88PhefsTer?
XR_934513.3:n.1116del
XR_934514.3:n.1116del
NM_058216.3:c.612del MANE Select	NP_478123.1:p.Leu205PhefsTer?
NR_103872.2:n.487del