Canonical Allele Identifier: CA658658641

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 471445
• ClinVar RCV Id: RCV000546881
• dbSNP Id: rs1555594864
• MyVariant Identifiers: chr17:g.56774184del (hg19) ; chr17:g.58696823del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58696823del , CM000679.2:g.58696823del	GRCh38
NC_000017.10:g.56774184del , CM000679.1:g.56774184del	GRCh37
NC_000017.9:g.54129183del	NCBI36
NG_023199.1:g.9222del , LRG_314:g.9222del
NG_047169.1:g.257del

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.184del	ENSP00000464056.2:p.His62ThrfsTer5
ENST00000697675.1:n.3132del
ENST00000697676.1:n.595del
ENST00000697677.1:n.1616del
ENST00000697678.1:n.437del
ENST00000697679.1:n.1609del
ENST00000697680.1:c.*1399del	ENSP00000513392.1:n.*1399del
ENST00000697681.1:c.*1426del	ENSP00000513393.1:n.*1426del
ENST00000697683.1:c.*1399del	ENSP00000513395.1:n.*1399del
ENST00000697684.1:n.595del
ENST00000697685.1:c.*1268+1634del	ENSP00000513396.1:n.*1268+1634del
ENST00000697686.1:c.184del	ENSP00000513397.1:p.His62ThrfsTer5
ENST00000697687.1:n.450+1634del
ENST00000697688.1:n.581del
ENST00000697689.1:c.*1107+1634del	ENSP00000513398.1:n.*1107+1634del
ENST00000697690.1:c.535del	ENSP00000513399.1:p.His179ThrfsTer5
ENST00000697691.1:c.*507del	ENSP00000513400.1:n.*507del
ENST00000697692.1:c.*547del	ENSP00000513401.1:n.*547del
ENST00000697694.1:c.184del	ENSP00000513402.1:p.His62ThrfsTer5
ENST00000697695.1:n.1142del
ENST00000337432.9:c.535del MANE Select	ENSP00000336701.4:p.His179ThrfsTer5
ENST00000337432.8:c.535del	ENSP00000336701.4:p.His179ThrfsTer5
ENST00000413590.5:c.173del
ENST00000425173.5:c.331del	ENSP00000407282.1:p.His111ThrfsTer5
ENST00000461271.5:c.184del	ENSP00000464056.1:p.His62ThrfsTer5
ENST00000475762.5:c.*1238del	ENSP00000432421.1:n.*1238del
ENST00000482007.5:c.404+1634del	ENSP00000433332.1:n.404+1634del
ENST00000487525.5:c.404+1634del	ENSP00000431637.1:n.404+1634del
ENST00000487921.5:n.447del
ENST00000583539.5:c.535del	ENSP00000463121.1:p.His179ThrfsTer5
ENST00000584617.5:c.257del
ENST00000622327.4:c.271del	ENSP00000482326.1:p.His91ThrfsTer5
NM_058216.2:c.535del	NP_478123.1:p.His179ThrfsTer5
NR_103872.1:n.475+1634del
XM_006722001.2:c.535del	XP_006722064.1:p.His179ThrfsTer5
XM_006722002.2:c.535del	XP_006722065.1:p.His179ThrfsTer5
XM_006722004.2:c.184del	XP_006722067.1:p.His62ThrfsTer5
XM_006722005.2:c.184del	XP_006722068.1:p.His62ThrfsTer5
XM_011525092.1:c.184del	XP_011523394.1:p.His62ThrfsTer5
XM_011525093.1:c.184del	XP_011523395.1:p.His62ThrfsTer5
XM_011525094.1:c.184del	XP_011523396.1:p.His62ThrfsTer5
XR_934513.1:n.608del
XR_934514.1:n.608del
XM_006722001.4:c.535del	XP_006722064.1:p.His179ThrfsTer5
XM_006722002.4:c.535del	XP_006722065.1:p.His179ThrfsTer5
XM_006722004.3:c.184del	XP_006722067.1:p.His62ThrfsTer5
XM_006722005.3:c.184del	XP_006722068.1:p.His62ThrfsTer5
XM_011525092.2:c.184del	XP_011523394.1:p.His62ThrfsTer5
XM_011525093.2:c.184del	XP_011523395.1:p.His62ThrfsTer5
XM_011525094.2:c.184del	XP_011523396.1:p.His62ThrfsTer5
XM_017024914.1:c.184del	XP_016880403.1:p.His62ThrfsTer5
XM_017024915.1:c.184del	XP_016880404.1:p.His62ThrfsTer5
XM_017024916.1:c.184del	XP_016880405.1:p.His62ThrfsTer5
XM_017024917.1:c.184del	XP_016880406.1:p.His62ThrfsTer5
XM_017024918.2:c.184del	XP_016880407.1:p.His62ThrfsTer5
XM_017024919.1:c.184del	XP_016880408.1:p.His62ThrfsTer5
XR_934513.3:n.1039del
XR_934514.3:n.1039del
NM_058216.3:c.535del MANE Select	NP_478123.1:p.His179ThrfsTer5
NR_103872.2:n.446+1634del