Canonical Allele Identifier: CA400353641

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 2692008
• ClinVar RCV Id: RCV003494205
• dbSNP Id: rs2143851942
• MyVariant Identifiers: chr17:g.56787271G>A (hg19) ; chr17:g.58709910G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58709910G>A , CM000679.2:g.58709910G>A	GRCh38
NC_000017.10:g.56787271G>A , CM000679.1:g.56787271G>A	GRCh37
NC_000017.9:g.54142270G>A	NCBI36
NG_023199.1:g.22309G>A , LRG_314:g.22309G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.406G>A	ENSP00000464056.2:p.Asp136Asn
ENST00000697678.1:n.659G>A
ENST00000697679.1:n.1831G>A
ENST00000697680.1:c.*1621G>A	ENSP00000513392.1:n.*1621G>A
ENST00000697681.1:c.*1918G>A	ENSP00000513393.1:n.*1918G>A
ENST00000697683.1:c.*1621G>A	ENSP00000513395.1:n.*1621G>A
ENST00000697684.1:n.817G>A
ENST00000697685.1:c.*1454G>A	ENSP00000513396.1:n.*1454G>A
ENST00000697686.1:c.406G>A	ENSP00000513397.1:p.Asp136Asn
ENST00000697687.1:n.636G>A
ENST00000697688.1:n.803G>A
ENST00000697689.1:c.*1293G>A	ENSP00000513398.1:n.*1293G>A
ENST00000697690.1:c.757G>A	ENSP00000513399.1:p.Asp253Asn
ENST00000697691.1:c.*729G>A	ENSP00000513400.1:n.*729G>A
ENST00000697692.1:c.*769G>A	ENSP00000513401.1:n.*769G>A
ENST00000697694.1:c.406G>A	ENSP00000513402.1:p.Asp136Asn
ENST00000697695.1:n.1364G>A
ENST00000337432.9:c.757G>A MANE Select	ENSP00000336701.4:p.Asp253Asn
ENST00000337432.8:c.757G>A	ENSP00000336701.4:p.Asp253Asn
ENST00000413590.5:c.395G>A
ENST00000461271.5:c.406G>A
ENST00000475762.5:c.*1460G>A	ENSP00000432421.1:n.*1460G>A
ENST00000482007.5:c.*185G>A	ENSP00000433332.1:n.*185G>A
ENST00000487525.5:c.*330G>A	ENSP00000431637.1:n.*330G>A
ENST00000578151.1:n.92G>A
ENST00000581221.5:n.272G>A
ENST00000583539.5:c.757G>A	ENSP00000463121.1:p.Asp253Asn
ENST00000584617.5:c.479G>A
ENST00000584804.1:c.52G>A	ENSP00000463658.1:p.Asp18Asn
NM_058216.2:c.757G>A	NP_478123.1:p.Asp253Asn
NR_103872.1:n.661G>A
XM_006722001.2:c.757G>A	XP_006722064.1:p.Asp253Asn
XM_006722002.2:c.757G>A	XP_006722065.1:p.Asp253Asn
XM_006722004.2:c.406G>A	XP_006722067.1:p.Asp136Asn
XM_006722005.2:c.406G>A	XP_006722068.1:p.Asp136Asn
XM_011525092.1:c.406G>A	XP_011523394.1:p.Asp136Asn
XM_011525093.1:c.406G>A	XP_011523395.1:p.Asp136Asn
XM_011525094.1:c.406G>A	XP_011523396.1:p.Asp136Asn
XR_934513.1:n.975G>A
XR_934514.1:n.975G>A
XM_006722001.4:c.757G>A	XP_006722064.1:p.Asp253Asn
XM_006722002.4:c.757G>A	XP_006722065.1:p.Asp253Asn
XM_006722004.3:c.406G>A	XP_006722067.1:p.Asp136Asn
XM_006722005.3:c.406G>A	XP_006722068.1:p.Asp136Asn
XM_011525092.2:c.406G>A	XP_011523394.1:p.Asp136Asn
XM_011525093.2:c.406G>A	XP_011523395.1:p.Asp136Asn
XM_011525094.2:c.406G>A	XP_011523396.1:p.Asp136Asn
XM_017024914.1:c.406G>A	XP_016880403.1:p.Asp136Asn
XM_017024915.1:c.406G>A	XP_016880404.1:p.Asp136Asn
XM_017024916.1:c.406G>A	XP_016880405.1:p.Asp136Asn
XM_017024917.1:c.406G>A	XP_016880406.1:p.Asp136Asn
XM_017024918.2:c.406G>A	XP_016880407.1:p.Asp136Asn
XM_017024919.1:c.406G>A	XP_016880408.1:p.Asp136Asn
XR_934513.3:n.1406G>A
XR_934514.3:n.1406G>A
NM_058216.3:c.757G>A MANE Select	NP_478123.1:p.Asp253Asn
NR_103872.2:n.632G>A