Canonical Allele Identifier: CA916081892

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 844507
• ClinVar RCV Id: RCV001047371
• dbSNP Id: rs2048274544

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703299del , CM000679.2:g.58703299del	GRCh38
NC_000017.10:g.56780660del , CM000679.1:g.56780660del	GRCh37
NC_000017.9:g.54135659del	NCBI36
NG_023199.1:g.15698del , LRG_314:g.15698del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.324del	ENSP00000464056.2:p.Leu109PhefsTer13
ENST00000697677.1:n.1756del
ENST00000697678.1:n.577del
ENST00000697679.1:n.1749del
ENST00000697680.1:c.*1539del	ENSP00000513392.1:n.*1539del
ENST00000697681.1:c.*1691del	ENSP00000513393.1:n.*1691del
ENST00000697683.1:c.*1539del	ENSP00000513395.1:n.*1539del
ENST00000697684.1:n.735del
ENST00000697685.1:c.*1372del	ENSP00000513396.1:n.*1372del
ENST00000697686.1:c.324del	ENSP00000513397.1:p.Leu109PhefsTer13
ENST00000697687.1:n.554del
ENST00000697688.1:n.721del
ENST00000697689.1:c.*1211del	ENSP00000513398.1:n.*1211del
ENST00000697690.1:c.675del	ENSP00000513399.1:p.Leu226PhefsTer13
ENST00000697691.1:c.*647del	ENSP00000513400.1:n.*647del
ENST00000697692.1:c.*687del	ENSP00000513401.1:n.*687del
ENST00000697694.1:c.324del	ENSP00000513402.1:p.Leu109PhefsTer13
ENST00000697695.1:n.1282del
ENST00000337432.9:c.675del MANE Select	ENSP00000336701.4:p.Leu226PhefsTer13
ENST00000337432.8:c.675del	ENSP00000336701.4:p.Leu226PhefsTer13
ENST00000413590.5:c.313del
ENST00000425173.5:c.471del	ENSP00000407282.1:p.Leu158PhefsTer?
ENST00000461271.5:c.324del	ENSP00000464056.1:p.Leu109PhefsTer13
ENST00000475762.5:c.*1378del	ENSP00000432421.1:n.*1378del
ENST00000482007.5:c.*103del	ENSP00000433332.1:n.*103del
ENST00000487525.5:c.*103del	ENSP00000431637.1:n.*103del
ENST00000487921.5:n.587del
ENST00000583539.5:c.675del	ENSP00000463121.1:p.Leu226PhefsTer13
ENST00000584617.5:c.397del
NM_058216.2:c.675del	NP_478123.1:p.Leu226PhefsTer13
NR_103872.1:n.579del
XM_006722001.2:c.675del	XP_006722064.1:p.Leu226PhefsTer13
XM_006722002.2:c.675del	XP_006722065.1:p.Leu226PhefsTer13
XM_006722004.2:c.324del	XP_006722067.1:p.Leu109PhefsTer13
XM_006722005.2:c.324del	XP_006722068.1:p.Leu109PhefsTer13
XM_011525092.1:c.324del	XP_011523394.1:p.Leu109PhefsTer13
XM_011525093.1:c.324del	XP_011523395.1:p.Leu109PhefsTer13
XM_011525094.1:c.324del	XP_011523396.1:p.Leu109PhefsTer13
XR_934513.1:n.748del
XR_934514.1:n.748del
XM_006722001.4:c.675del	XP_006722064.1:p.Leu226PhefsTer13
XM_006722002.4:c.675del	XP_006722065.1:p.Leu226PhefsTer13
XM_006722004.3:c.324del	XP_006722067.1:p.Leu109PhefsTer13
XM_006722005.3:c.324del	XP_006722068.1:p.Leu109PhefsTer13
XM_011525092.2:c.324del	XP_011523394.1:p.Leu109PhefsTer13
XM_011525093.2:c.324del	XP_011523395.1:p.Leu109PhefsTer13
XM_011525094.2:c.324del	XP_011523396.1:p.Leu109PhefsTer13
XM_017024914.1:c.324del	XP_016880403.1:p.Leu109PhefsTer13
XM_017024915.1:c.324del	XP_016880404.1:p.Leu109PhefsTer13
XM_017024916.1:c.324del	XP_016880405.1:p.Leu109PhefsTer13
XM_017024917.1:c.324del	XP_016880406.1:p.Leu109PhefsTer13
XM_017024918.2:c.324del	XP_016880407.1:p.Leu109PhefsTer13
XM_017024919.1:c.324del	XP_016880408.1:p.Leu109PhefsTer13
XR_934513.3:n.1179del
XR_934514.3:n.1179del
NM_058216.3:c.675del MANE Select	NP_478123.1:p.Leu226PhefsTer13
NR_103872.2:n.550del