Canonical Allele Identifier: CA2740093812

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 3022684
• ClinVar RCV Id: RCV003881870

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692800T>C , CM000679.2:g.58692800T>C	GRCh38
NC_000017.10:g.56770161T>C , CM000679.1:g.56770161T>C	GRCh37
NC_000017.9:g.54125160T>C	NCBI36
NG_023199.1:g.5199T>C , LRG_314:g.5199T>C
NG_047169.1:g.4280A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-207+115T>C	ENSP00000464056.2:n.-207+115T>C
ENST00000697675.1:n.228T>C
ENST00000697676.1:n.205+12T>C
ENST00000697677.1:n.215T>C
ENST00000697678.1:n.47+168T>C
ENST00000697679.1:n.208T>C
ENST00000697680.1:c.157T>C	ENSP00000513392.1:p.Ter53Arg
ENST00000697681.1:c.157T>C	ENSP00000513393.1:p.Ter53Arg
ENST00000697683.1:c.157T>C	ENSP00000513395.1:p.Ter53Arg
ENST00000697684.1:n.205+12T>C
ENST00000697685.1:c.157T>C	ENSP00000513396.1:p.Ter53Arg
ENST00000697686.1:c.-207+168T>C	ENSP00000513397.1:n.-207+168T>C
ENST00000697687.1:n.191+12T>C
ENST00000697688.1:n.191+12T>C
ENST00000697689.1:c.157T>C	ENSP00000513398.1:p.Ter53Arg
ENST00000697690.1:c.145+12T>C	ENSP00000513399.1:n.145+12T>C
ENST00000697691.1:c.42+115T>C	ENSP00000513400.1:n.42+115T>C
ENST00000697692.1:c.157T>C	ENSP00000513401.1:p.Ter53Arg
ENST00000697693.1:n.70T>C
ENST00000337432.9:c.145+12T>C MANE Select	ENSP00000336701.4:n.145+12T>C
ENST00000337432.8:c.145+12T>C	ENSP00000336701.4:n.145+12T>C
ENST00000421782.3:c.145+12T>C	ENSP00000391450.2:n.145+12T>C
ENST00000461271.5:c.-207+115T>C	ENSP00000464056.1:n.-207+115T>C
ENST00000475762.5:c.157T>C	ENSP00000432421.1:p.Ter53Arg
ENST00000476741.2:n.187+12T>C
ENST00000482007.5:c.145+12T>C	ENSP00000433332.1:n.145+12T>C
ENST00000486827.1:c.157T>C	ENSP00000436761.1:p.Ter53Arg
ENST00000487525.5:c.145+12T>C	ENSP00000431637.1:n.145+12T>C
ENST00000487921.5:n.57+168T>C
ENST00000583539.5:c.145+12T>C	ENSP00000463121.1:n.145+12T>C
ENST00000584617.5:c.126+12T>C
NM_002876.3:c.145+12T>C	NP_002867.1:n.145+12T>C
NM_058216.2:c.145+12T>C	NP_478123.1:n.145+12T>C
NR_103872.1:n.216+12T>C
NR_103873.1:n.113+115T>C
XM_006722001.2:c.145+12T>C	XP_006722064.1:n.145+12T>C
XM_006722002.2:c.145+12T>C	XP_006722065.1:n.145+12T>C
XM_006722004.2:c.-207+115T>C	XP_006722067.1:n.-207+115T>C
XM_006722005.2:c.-207+168T>C	XP_006722068.1:n.-207+168T>C
XM_011525092.1:c.-507+115T>C	XP_011523394.1:n.-507+115T>C
XM_011525093.1:c.-668+115T>C	XP_011523395.1:n.-668+115T>C
XR_934513.1:n.218+12T>C
XR_934514.1:n.218+12T>C
XM_006722001.4:c.145+12T>C	XP_006722064.1:n.145+12T>C
XM_006722002.4:c.145+12T>C	XP_006722065.1:n.145+12T>C
XM_006722004.3:c.-207+115T>C	XP_006722067.1:n.-207+115T>C
XM_006722005.3:c.-207+168T>C	XP_006722068.1:n.-207+168T>C
XM_011525092.2:c.-507+115T>C	XP_011523394.1:n.-507+115T>C
XM_011525093.2:c.-668+115T>C	XP_011523395.1:n.-668+115T>C
XM_011525094.2:c.-366T>C	XP_011523396.1:n.-366T>C
XM_017024914.1:c.-207+115T>C	XP_016880403.1:n.-207+115T>C
XM_017024916.1:c.-507+115T>C	XP_016880405.1:n.-507+115T>C
XM_017024917.1:c.-207+168T>C	XP_016880406.1:n.-207+168T>C
XM_017024918.2:c.-366T>C	XP_016880407.1:n.-366T>C
XM_017024919.1:c.-668+115T>C	XP_016880408.1:n.-668+115T>C
XR_934513.3:n.649+12T>C
XR_934514.3:n.649+12T>C
NM_058216.3:c.145+12T>C MANE Select	NP_478123.1:n.145+12T>C
NR_103872.2:n.187+12T>C
NM_002876.4:c.145+12T>C	NP_002867.1:n.145+12T>C