Canonical Allele Identifier: CA2573054499

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 1330083
• ClinVar RCV Id: RCV001801100
• dbSNP Id: rs2143801832

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703316_58703318delinsAA , CM000679.2:g.58703316_58703318delinsAA	GRCh38
NC_000017.10:g.56780677_56780679delinsAA , CM000679.1:g.56780677_56780679delinsAA	GRCh37
NC_000017.9:g.54135676_54135678delinsAA	NCBI36
NG_023199.1:g.15715_15717delinsAA , LRG_314:g.15715_15717delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.341_343delinsAA	ENSP00000464056.2:p.Ser114Ter
ENST00000697677.1:n.1773_1775delinsAA
ENST00000697678.1:n.594_596delinsAA
ENST00000697679.1:n.1766_1768delinsAA
ENST00000697680.1:c.*1556_*1558delinsAA	ENSP00000513392.1:n.*1556_*1558delinsAA
ENST00000697681.1:c.*1708_*1710delinsAA	ENSP00000513393.1:n.*1708_*1710delinsAA
ENST00000697683.1:c.*1556_*1558delinsAA	ENSP00000513395.1:n.*1556_*1558delinsAA
ENST00000697684.1:n.752_754delinsAA
ENST00000697685.1:c.*1389_*1391delinsAA	ENSP00000513396.1:n.*1389_*1391delinsAA
ENST00000697686.1:c.341_343delinsAA	ENSP00000513397.1:p.Ser114Ter
ENST00000697687.1:n.571_573delinsAA
ENST00000697688.1:n.738_740delinsAA
ENST00000697689.1:c.*1228_*1230delinsAA	ENSP00000513398.1:n.*1228_*1230delinsAA
ENST00000697690.1:c.692_694delinsAA	ENSP00000513399.1:p.Ser231Ter
ENST00000697691.1:c.*664_*666delinsAA	ENSP00000513400.1:n.*664_*666delinsAA
ENST00000697692.1:c.*704_*706delinsAA	ENSP00000513401.1:n.*704_*706delinsAA
ENST00000697694.1:c.341_343delinsAA	ENSP00000513402.1:p.Ser114Ter
ENST00000697695.1:n.1299_1301delinsAA
ENST00000337432.9:c.692_694delinsAA MANE Select	ENSP00000336701.4:p.Ser231Ter
ENST00000337432.8:c.692_694delinsAA	ENSP00000336701.4:p.Ser231Ter
ENST00000413590.5:c.330_332delinsAA
ENST00000425173.5:c.488_490delinsAA	ENSP00000407282.1:p.Ser163Ter
ENST00000461271.5:c.341_343delinsAA	ENSP00000464056.1:p.Ser114Ter
ENST00000475762.5:c.*1395_*1397delinsAA	ENSP00000432421.1:n.*1395_*1397delinsAA
ENST00000482007.5:c.*120_*122delinsAA	ENSP00000433332.1:n.*120_*122delinsAA
ENST00000487525.5:c.*120_*122delinsAA	ENSP00000431637.1:n.*120_*122delinsAA
ENST00000487921.5:n.604_606delinsAA
ENST00000583539.5:c.692_694delinsAA	ENSP00000463121.1:p.Ser231Ter
ENST00000584617.5:c.414_416delinsAA
NM_058216.2:c.692_694delinsAA	NP_478123.1:p.Ser231Ter
NR_103872.1:n.596_598delinsAA
XM_006722001.2:c.692_694delinsAA	XP_006722064.1:p.Ser231Ter
XM_006722002.2:c.692_694delinsAA	XP_006722065.1:p.Ser231Ter
XM_006722004.2:c.341_343delinsAA	XP_006722067.1:p.Ser114Ter
XM_006722005.2:c.341_343delinsAA	XP_006722068.1:p.Ser114Ter
XM_011525092.1:c.341_343delinsAA	XP_011523394.1:p.Ser114Ter
XM_011525093.1:c.341_343delinsAA	XP_011523395.1:p.Ser114Ter
XM_011525094.1:c.341_343delinsAA	XP_011523396.1:p.Ser114Ter
XR_934513.1:n.765_767delinsAA
XR_934514.1:n.765_767delinsAA
XM_006722001.4:c.692_694delinsAA	XP_006722064.1:p.Ser231Ter
XM_006722002.4:c.692_694delinsAA	XP_006722065.1:p.Ser231Ter
XM_006722004.3:c.341_343delinsAA	XP_006722067.1:p.Ser114Ter
XM_006722005.3:c.341_343delinsAA	XP_006722068.1:p.Ser114Ter
XM_011525092.2:c.341_343delinsAA	XP_011523394.1:p.Ser114Ter
XM_011525093.2:c.341_343delinsAA	XP_011523395.1:p.Ser114Ter
XM_011525094.2:c.341_343delinsAA	XP_011523396.1:p.Ser114Ter
XM_017024914.1:c.341_343delinsAA	XP_016880403.1:p.Ser114Ter
XM_017024915.1:c.341_343delinsAA	XP_016880404.1:p.Ser114Ter
XM_017024916.1:c.341_343delinsAA	XP_016880405.1:p.Ser114Ter
XM_017024917.1:c.341_343delinsAA	XP_016880406.1:p.Ser114Ter
XM_017024918.2:c.341_343delinsAA	XP_016880407.1:p.Ser114Ter
XM_017024919.1:c.341_343delinsAA	XP_016880408.1:p.Ser114Ter
XR_934513.3:n.1196_1198delinsAA
XR_934514.3:n.1196_1198delinsAA
NM_058216.3:c.692_694delinsAA MANE Select	NP_478123.1:p.Ser231Ter
NR_103872.2:n.567_569delinsAA