Canonical Allele Identifier: CA658684139

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 492399
• ClinVar RCV Id: RCV000584392 ; RCV000701832 ; RCV003451314
• dbSNP Id: rs1555603056
• gnomAD v4: 17-58724096-CA-C
• MyVariant Identifiers: chr17:g.56801460del (hg19) ; chr17:g.58724099del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58724099del , CM000679.2:g.58724099del	GRCh38
NC_000017.10:g.56801460del , CM000679.1:g.56801460del	GRCh37
NC_000017.9:g.54156459del	NCBI36
NG_023199.1:g.36498del , LRG_314:g.36498del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.613del	ENSP00000464056.2:p.Arg205GlyfsTer27
ENST00000697680.1:c.*1928del	ENSP00000513392.1:n.*1928del
ENST00000697681.1:c.*2125del	ENSP00000513393.1:n.*2125del
ENST00000697683.1:c.*1828del	ENSP00000513395.1:n.*1828del
ENST00000697684.1:n.1024del
ENST00000697685.1:c.*1661del	ENSP00000513396.1:n.*1661del
ENST00000697686.1:c.613del	ENSP00000513397.1:p.Arg205AspfsTer?
ENST00000697687.1:n.843del
ENST00000697688.1:n.1010del
ENST00000697689.1:c.*1440+3287del	ENSP00000513398.1:n.*1440+3287del
ENST00000697690.1:c.904+3287del	ENSP00000513399.1:n.904+3287del
ENST00000697691.1:c.*936del	ENSP00000513400.1:n.*936del
ENST00000697692.1:c.*976del	ENSP00000513401.1:n.*976del
ENST00000697694.1:c.613del	ENSP00000513402.1:p.Arg205GlyfsTer?
ENST00000697695.1:n.1571del
ENST00000337432.9:c.964del MANE Select	ENSP00000336701.4:p.Arg322GlyfsTer?
ENST00000337432.8:c.964del	ENSP00000336701.4:p.Arg322GlyfsTer?
ENST00000413590.5:c.602del
ENST00000475762.5:c.*1600del	ENSP00000432421.1:n.*1600del
ENST00000482007.5:c.*392del	ENSP00000433332.1:n.*392del
ENST00000487525.5:c.*537del	ENSP00000431637.1:n.*537del
ENST00000578151.1:n.239+3287del
ENST00000581221.5:n.479del
ENST00000583539.5:c.964del	ENSP00000463121.1:p.Arg322GlyfsTer27
ENST00000584617.5:c.686del
ENST00000584804.1:c.199+3287del	ENSP00000463658.1:n.199+3287del
NM_058216.2:c.964del	NP_478123.1:p.Arg322GlyfsTer?
NR_103872.1:n.868del
XM_006722001.2:c.964del	XP_006722064.1:p.Ser322AlafsTer?
XM_006722002.2:c.904+3287del	XP_006722065.1:n.904+3287del
XM_006722004.2:c.613del	XP_006722067.1:p.Ser205AlafsTer?
XM_006722005.2:c.613del	XP_006722068.1:p.Ser205AlafsTer?
XM_011525092.1:c.613del	XP_011523394.1:p.Ser205AlafsTer?
XM_011525093.1:c.613del	XP_011523395.1:p.Ser205AlafsTer?
XM_011525094.1:c.613del	XP_011523396.1:p.Ser205AlafsTer?
XR_934513.1:n.1182del
XR_934514.1:n.1182del
XM_006722001.4:c.964del	XP_006722064.1:p.Ser322AlafsTer?
XM_006722002.4:c.904+3287del	XP_006722065.1:n.904+3287del
XM_006722004.3:c.613del	XP_006722067.1:p.Ser205AlafsTer?
XM_006722005.3:c.613del	XP_006722068.1:p.Ser205AlafsTer?
XM_011525092.2:c.613del	XP_011523394.1:p.Ser205AlafsTer?
XM_011525093.2:c.613del	XP_011523395.1:p.Ser205AlafsTer?
XM_011525094.2:c.613del	XP_011523396.1:p.Ser205AlafsTer?
XM_017024914.1:c.613del	XP_016880403.1:p.Arg205GlyfsTer?
XM_017024915.1:c.613del	XP_016880404.1:p.Arg205GlyfsTer?
XM_017024916.1:c.613del	XP_016880405.1:p.Arg205GlyfsTer?
XM_017024917.1:c.613del	XP_016880406.1:p.Arg205GlyfsTer?
XM_017024918.2:c.613del	XP_016880407.1:p.Arg205GlyfsTer?
XM_017024919.1:c.553+3287del	XP_016880408.1:n.553+3287del
XR_934513.3:n.1613del
XR_934514.3:n.1613del
NM_058216.3:c.964del MANE Select	NP_478123.1:p.Arg322GlyfsTer?
NR_103872.2:n.839del