Canonical Allele Identifier: CA2573054500

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 1098905
• ClinVar RCV Id: RCV001882538 ; RCV001779205
• dbSNP Id: rs1567794476

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703328dup , CM000679.2:g.58703328dup	GRCh38
NC_000017.10:g.56780689dup , CM000679.1:g.56780689dup	GRCh37
NC_000017.9:g.54135688dup	NCBI36
NG_023199.1:g.15727dup , LRG_314:g.15727dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.353dup	ENSP00000464056.2:p.Val119GlyfsTer16
ENST00000697677.1:n.1785dup
ENST00000697678.1:n.606dup
ENST00000697679.1:n.1778dup
ENST00000697680.1:c.*1568dup	ENSP00000513392.1:n.*1568dup
ENST00000697681.1:c.*1720dup	ENSP00000513393.1:n.*1720dup
ENST00000697683.1:c.*1568dup	ENSP00000513395.1:n.*1568dup
ENST00000697684.1:n.764dup
ENST00000697685.1:c.*1401dup	ENSP00000513396.1:n.*1401dup
ENST00000697686.1:c.353dup	ENSP00000513397.1:p.Val119GlyfsTer16
ENST00000697687.1:n.583dup
ENST00000697688.1:n.750dup
ENST00000697689.1:c.*1240dup	ENSP00000513398.1:n.*1240dup
ENST00000697690.1:c.704dup	ENSP00000513399.1:p.Val236GlyfsTer16
ENST00000697691.1:c.*676dup	ENSP00000513400.1:n.*676dup
ENST00000697692.1:c.*716dup	ENSP00000513401.1:n.*716dup
ENST00000697694.1:c.353dup	ENSP00000513402.1:p.Val119GlyfsTer16
ENST00000697695.1:n.1311dup
ENST00000337432.9:c.704dup MANE Select	ENSP00000336701.4:p.Val236GlyfsTer16
ENST00000337432.8:c.704dup	ENSP00000336701.4:p.Val236GlyfsTer16
ENST00000413590.5:c.342dup
ENST00000425173.5:c.500dup	ENSP00000407282.1:p.Ala168GlyfsTer5
ENST00000461271.5:c.353dup	ENSP00000464056.1:p.Val119GlyfsTer16
ENST00000475762.5:c.*1407dup	ENSP00000432421.1:n.*1407dup
ENST00000482007.5:c.*132dup	ENSP00000433332.1:n.*132dup
ENST00000487525.5:c.*132dup	ENSP00000431637.1:n.*132dup
ENST00000487921.5:n.616dup
ENST00000583539.5:c.704dup	ENSP00000463121.1:p.Val236GlyfsTer16
ENST00000584617.5:c.426dup
NM_058216.2:c.704dup	NP_478123.1:p.Val236GlyfsTer16
NR_103872.1:n.608dup
XM_006722001.2:c.704dup	XP_006722064.1:p.Val236GlyfsTer16
XM_006722002.2:c.704dup	XP_006722065.1:p.Val236GlyfsTer16
XM_006722004.2:c.353dup	XP_006722067.1:p.Val119GlyfsTer16
XM_006722005.2:c.353dup	XP_006722068.1:p.Val119GlyfsTer16
XM_011525092.1:c.353dup	XP_011523394.1:p.Val119GlyfsTer16
XM_011525093.1:c.353dup	XP_011523395.1:p.Val119GlyfsTer16
XM_011525094.1:c.353dup	XP_011523396.1:p.Val119GlyfsTer16
XR_934513.1:n.777dup
XR_934514.1:n.777dup
XM_006722001.4:c.704dup	XP_006722064.1:p.Val236GlyfsTer16
XM_006722002.4:c.704dup	XP_006722065.1:p.Val236GlyfsTer16
XM_006722004.3:c.353dup	XP_006722067.1:p.Val119GlyfsTer16
XM_006722005.3:c.353dup	XP_006722068.1:p.Val119GlyfsTer16
XM_011525092.2:c.353dup	XP_011523394.1:p.Val119GlyfsTer16
XM_011525093.2:c.353dup	XP_011523395.1:p.Val119GlyfsTer16
XM_011525094.2:c.353dup	XP_011523396.1:p.Val119GlyfsTer16
XM_017024914.1:c.353dup	XP_016880403.1:p.Val119GlyfsTer16
XM_017024915.1:c.353dup	XP_016880404.1:p.Val119GlyfsTer16
XM_017024916.1:c.353dup	XP_016880405.1:p.Val119GlyfsTer16
XM_017024917.1:c.353dup	XP_016880406.1:p.Val119GlyfsTer16
XM_017024918.2:c.353dup	XP_016880407.1:p.Val119GlyfsTer16
XM_017024919.1:c.353dup	XP_016880408.1:p.Val119GlyfsTer16
XR_934513.3:n.1208dup
XR_934514.3:n.1208dup
NM_058216.3:c.704dup MANE Select	NP_478123.1:p.Val236GlyfsTer16
NR_103872.2:n.579dup