Canonical Allele Identifier: CA2580094337

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 2447778
• ClinVar RCV Id: RCV003168021

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692765del , CM000679.2:g.58692765del	GRCh38
NC_000017.10:g.56770126del , CM000679.1:g.56770126del	GRCh37
NC_000017.9:g.54125125del	NCBI36
NG_023199.1:g.5164del , LRG_314:g.5164del
NG_047169.1:g.4315del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-207+80del	ENSP00000464056.2:n.-207+80del
ENST00000697675.1:n.193del
ENST00000697676.1:n.182del
ENST00000697677.1:n.180del
ENST00000697678.1:n.47+133del
ENST00000697679.1:n.173del
ENST00000697680.1:c.122del	ENSP00000513392.1:p.Val41GlyfsTer?
ENST00000697681.1:c.122del	ENSP00000513393.1:p.Val41GlyfsTer?
ENST00000697683.1:c.122del	ENSP00000513395.1:p.Val41GlyfsTer?
ENST00000697684.1:n.182del
ENST00000697685.1:c.122del	ENSP00000513396.1:p.Val41GlyfsTer?
ENST00000697686.1:c.-207+133del	ENSP00000513397.1:n.-207+133del
ENST00000697687.1:n.168del
ENST00000697688.1:n.168del
ENST00000697689.1:c.122del	ENSP00000513398.1:p.Val41GlyfsTer?
ENST00000697690.1:c.122del	ENSP00000513399.1:p.Val41GlyfsTer18
ENST00000697691.1:c.42+80del	ENSP00000513400.1:n.42+80del
ENST00000697692.1:c.122del	ENSP00000513401.1:p.Val41GlyfsTer?
ENST00000697693.1:n.35del
ENST00000337432.9:c.122del MANE Select	ENSP00000336701.4:p.Val41GlyfsTer18
ENST00000337432.8:c.122del	ENSP00000336701.4:p.Val41GlyfsTer18
ENST00000421782.3:c.122del	ENSP00000391450.2:p.Val41GlyfsTer18
ENST00000461271.5:c.-207+80del	ENSP00000464056.1:n.-207+80del
ENST00000475762.5:c.122del	ENSP00000432421.1:p.Val41GlyfsTer?
ENST00000476741.2:n.164del
ENST00000482007.5:c.122del	ENSP00000433332.1:p.Val41GlyfsTer18
ENST00000486827.1:c.122del	ENSP00000436761.1:p.Val41GlyfsTer?
ENST00000487525.5:c.122del	ENSP00000431637.1:p.Val41GlyfsTer18
ENST00000487921.5:n.57+133del
ENST00000583539.5:c.122del	ENSP00000463121.1:p.Val41GlyfsTer18
ENST00000584617.5:c.103del
NM_002876.3:c.122del	NP_002867.1:p.Val41GlyfsTer18
NM_058216.2:c.122del	NP_478123.1:p.Val41GlyfsTer18
NR_103872.1:n.193del
NR_103873.1:n.113+80del
XM_006722001.2:c.122del	XP_006722064.1:p.Val41GlyfsTer18
XM_006722002.2:c.122del	XP_006722065.1:p.Val41GlyfsTer18
XM_006722004.2:c.-207+80del	XP_006722067.1:n.-207+80del
XM_006722005.2:c.-207+133del	XP_006722068.1:n.-207+133del
XM_011525092.1:c.-507+80del	XP_011523394.1:n.-507+80del
XM_011525093.1:c.-668+80del	XP_011523395.1:n.-668+80del
XR_934513.1:n.195del
XR_934514.1:n.195del
XM_006722001.4:c.122del	XP_006722064.1:p.Val41GlyfsTer18
XM_006722002.4:c.122del	XP_006722065.1:p.Val41GlyfsTer18
XM_006722004.3:c.-207+80del	XP_006722067.1:n.-207+80del
XM_006722005.3:c.-207+133del	XP_006722068.1:n.-207+133del
XM_011525092.2:c.-507+80del	XP_011523394.1:n.-507+80del
XM_011525093.2:c.-668+80del	XP_011523395.1:n.-668+80del
XM_017024914.1:c.-207+80del	XP_016880403.1:n.-207+80del
XM_017024916.1:c.-507+80del	XP_016880405.1:n.-507+80del
XM_017024917.1:c.-207+133del	XP_016880406.1:n.-207+133del
XM_017024918.2:c.-401del	XP_016880407.1:n.-401del
XM_017024919.1:c.-668+80del	XP_016880408.1:n.-668+80del
XR_934513.3:n.626del
XR_934514.3:n.626del
NM_058216.3:c.122del MANE Select	NP_478123.1:p.Val41GlyfsTer18
NR_103872.2:n.164del
NM_002876.4:c.122del	NP_002867.1:p.Val41GlyfsTer18