Canonical Allele Identifier: CA2825002571

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 3148699
• ClinVar RCV Id: RCV004442593

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58724040_58724043dup , CM000679.2:g.58724040_58724043dup	GRCh38
NC_000017.10:g.56801401_56801404dup , CM000679.1:g.56801401_56801404dup	GRCh37
NC_000017.9:g.54156400_54156403dup	NCBI36
NG_023199.1:g.36439_36442dup , LRG_314:g.36439_36442dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.554_557dup	ENSP00000464056.2:p.Ser187GlyfsTer?
ENST00000697680.1:c.*1869_*1872dup	ENSP00000513392.1:n.*1869_*1872dup
ENST00000697681.1:c.*2066_*2069dup	ENSP00000513393.1:n.*2066_*2069dup
ENST00000697683.1:c.*1769_*1772dup	ENSP00000513395.1:n.*1769_*1772dup
ENST00000697684.1:n.965_968dup
ENST00000697685.1:c.*1602_*1605dup	ENSP00000513396.1:n.*1602_*1605dup
ENST00000697686.1:c.554_557dup	ENSP00000513397.1:p.Ser187GlyfsTer?
ENST00000697687.1:n.784_787dup
ENST00000697688.1:n.951_954dup
ENST00000697689.1:c.*1440+3228_*1440+3231dup	ENSP00000513398.1:n.*1440+3228_*1440+3231dup
ENST00000697690.1:c.904+3228_904+3231dup	ENSP00000513399.1:n.904+3228_904+3231dup
ENST00000697691.1:c.*877_*880dup	ENSP00000513400.1:n.*877_*880dup
ENST00000697692.1:c.*917_*920dup	ENSP00000513401.1:n.*917_*920dup
ENST00000697694.1:c.554_557dup	ENSP00000513402.1:p.Ser187GlyfsTer?
ENST00000697695.1:n.1512_1515dup
ENST00000337432.9:c.905_908dup MANE Select	ENSP00000336701.4:p.Ser304GlyfsTer?
ENST00000337432.8:c.905_908dup	ENSP00000336701.4:p.Ser304GlyfsTer?
ENST00000413590.5:c.543_546dup
ENST00000475762.5:c.*1541_*1544dup	ENSP00000432421.1:n.*1541_*1544dup
ENST00000482007.5:c.*333_*336dup	ENSP00000433332.1:n.*333_*336dup
ENST00000487525.5:c.*478_*481dup	ENSP00000431637.1:n.*478_*481dup
ENST00000578151.1:n.239+3228_239+3231dup
ENST00000581221.5:n.420_423dup
ENST00000583539.5:c.905_908dup	ENSP00000463121.1:p.Ser304GlyfsTer?
ENST00000584617.5:c.627_630dup
ENST00000584804.1:c.199+3228_199+3231dup	ENSP00000463658.1:n.199+3228_199+3231dup
NM_058216.2:c.905_908dup	NP_478123.1:p.Ser304GlyfsTer?
NR_103872.1:n.809_812dup
XM_006722001.2:c.905_908dup	XP_006722064.1:p.Ser304GlyfsTer?
XM_006722002.2:c.904+3228_904+3231dup	XP_006722065.1:n.904+3228_904+3231dup
XM_006722004.2:c.554_557dup	XP_006722067.1:p.Ser187GlyfsTer?
XM_006722005.2:c.554_557dup	XP_006722068.1:p.Ser187GlyfsTer?
XM_011525092.1:c.554_557dup	XP_011523394.1:p.Ser187GlyfsTer?
XM_011525093.1:c.554_557dup	XP_011523395.1:p.Ser187GlyfsTer?
XM_011525094.1:c.554_557dup	XP_011523396.1:p.Ser187GlyfsTer?
XR_934513.1:n.1123_1126dup
XR_934514.1:n.1123_1126dup
XM_006722001.4:c.905_908dup	XP_006722064.1:p.Ser304GlyfsTer?
XM_006722002.4:c.904+3228_904+3231dup	XP_006722065.1:n.904+3228_904+3231dup
XM_006722004.3:c.554_557dup	XP_006722067.1:p.Ser187GlyfsTer?
XM_006722005.3:c.554_557dup	XP_006722068.1:p.Ser187GlyfsTer?
XM_011525092.2:c.554_557dup	XP_011523394.1:p.Ser187GlyfsTer?
XM_011525093.2:c.554_557dup	XP_011523395.1:p.Ser187GlyfsTer?
XM_011525094.2:c.554_557dup	XP_011523396.1:p.Ser187GlyfsTer?
XM_017024914.1:c.554_557dup	XP_016880403.1:p.Ser187GlyfsTer?
XM_017024915.1:c.554_557dup	XP_016880404.1:p.Ser187GlyfsTer?
XM_017024916.1:c.554_557dup	XP_016880405.1:p.Ser187GlyfsTer?
XM_017024917.1:c.554_557dup	XP_016880406.1:p.Ser187GlyfsTer?
XM_017024918.2:c.554_557dup	XP_016880407.1:p.Ser187GlyfsTer?
XM_017024919.1:c.553+3228_553+3231dup	XP_016880408.1:n.553+3228_553+3231dup
XR_934513.3:n.1554_1557dup
XR_934514.3:n.1554_1557dup
NM_058216.3:c.905_908dup MANE Select	NP_478123.1:p.Ser304GlyfsTer?
NR_103872.2:n.780_783dup