Canonical Allele Identifier: CA2573054497

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 1098902
• ClinVar RCV Id: RCV001779202
• dbSNP Id: rs2143798753

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703259del , CM000679.2:g.58703259del	GRCh38
NC_000017.10:g.56780620del , CM000679.1:g.56780620del	GRCh37
NC_000017.9:g.54135619del	NCBI36
NG_023199.1:g.15658del , LRG_314:g.15658del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.284del	ENSP00000464056.2:p.Arg95ProfsTer27
ENST00000697677.1:n.1716del
ENST00000697678.1:n.537del
ENST00000697679.1:n.1709del
ENST00000697680.1:c.*1499del	ENSP00000513392.1:n.*1499del
ENST00000697681.1:c.*1651del	ENSP00000513393.1:n.*1651del
ENST00000697683.1:c.*1499del	ENSP00000513395.1:n.*1499del
ENST00000697684.1:n.695del
ENST00000697685.1:c.*1332del	ENSP00000513396.1:n.*1332del
ENST00000697686.1:c.284del	ENSP00000513397.1:p.Arg95ProfsTer27
ENST00000697687.1:n.514del
ENST00000697688.1:n.681del
ENST00000697689.1:c.*1171del	ENSP00000513398.1:n.*1171del
ENST00000697690.1:c.635del	ENSP00000513399.1:p.Arg212ProfsTer27
ENST00000697691.1:c.*607del	ENSP00000513400.1:n.*607del
ENST00000697692.1:c.*647del	ENSP00000513401.1:n.*647del
ENST00000697694.1:c.284del	ENSP00000513402.1:p.Arg95ProfsTer27
ENST00000697695.1:n.1242del
ENST00000337432.9:c.635del MANE Select	ENSP00000336701.4:p.Arg212ProfsTer27
ENST00000337432.8:c.635del	ENSP00000336701.4:p.Arg212ProfsTer27
ENST00000413590.5:c.273del
ENST00000425173.5:c.431del	ENSP00000407282.1:p.Arg144ProfsTer?
ENST00000461271.5:c.284del	ENSP00000464056.1:p.Arg95ProfsTer27
ENST00000475762.5:c.*1338del	ENSP00000432421.1:n.*1338del
ENST00000482007.5:c.*63del	ENSP00000433332.1:n.*63del
ENST00000487525.5:c.*63del	ENSP00000431637.1:n.*63del
ENST00000487921.5:n.547del
ENST00000583539.5:c.635del	ENSP00000463121.1:p.Arg212ProfsTer27
ENST00000584617.5:c.357del
NM_058216.2:c.635del	NP_478123.1:p.Arg212ProfsTer27
NR_103872.1:n.539del
XM_006722001.2:c.635del	XP_006722064.1:p.Arg212ProfsTer27
XM_006722002.2:c.635del	XP_006722065.1:p.Arg212ProfsTer27
XM_006722004.2:c.284del	XP_006722067.1:p.Arg95ProfsTer27
XM_006722005.2:c.284del	XP_006722068.1:p.Arg95ProfsTer27
XM_011525092.1:c.284del	XP_011523394.1:p.Arg95ProfsTer27
XM_011525093.1:c.284del	XP_011523395.1:p.Arg95ProfsTer27
XM_011525094.1:c.284del	XP_011523396.1:p.Arg95ProfsTer27
XR_934513.1:n.708del
XR_934514.1:n.708del
XM_006722001.4:c.635del	XP_006722064.1:p.Arg212ProfsTer27
XM_006722002.4:c.635del	XP_006722065.1:p.Arg212ProfsTer27
XM_006722004.3:c.284del	XP_006722067.1:p.Arg95ProfsTer27
XM_006722005.3:c.284del	XP_006722068.1:p.Arg95ProfsTer27
XM_011525092.2:c.284del	XP_011523394.1:p.Arg95ProfsTer27
XM_011525093.2:c.284del	XP_011523395.1:p.Arg95ProfsTer27
XM_011525094.2:c.284del	XP_011523396.1:p.Arg95ProfsTer27
XM_017024914.1:c.284del	XP_016880403.1:p.Arg95ProfsTer27
XM_017024915.1:c.284del	XP_016880404.1:p.Arg95ProfsTer27
XM_017024916.1:c.284del	XP_016880405.1:p.Arg95ProfsTer27
XM_017024917.1:c.284del	XP_016880406.1:p.Arg95ProfsTer27
XM_017024918.2:c.284del	XP_016880407.1:p.Arg95ProfsTer27
XM_017024919.1:c.284del	XP_016880408.1:p.Arg95ProfsTer27
XR_934513.3:n.1139del
XR_934514.3:n.1139del
NM_058216.3:c.635del MANE Select	NP_478123.1:p.Arg212ProfsTer27
NR_103872.2:n.510del