Canonical Allele Identifier: CA2267814353

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58693200_58693201delinsGT , CM000679.2:g.58693200_58693201delinsGT	GRCh38
NC_000017.10:g.56770561_56770562delinsGT , CM000679.1:g.56770561_56770562delinsGT	GRCh37
NC_000017.9:g.54125560_54125561delinsGT	NCBI36
NG_023199.1:g.5599_5600delinsGT , LRG_314:g.5599_5600delinsGT
NG_047169.1:g.3879_3880delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-207+515_-207+516delinsGT	ENSP00000464056.2:n.-207+515_-207+516delinsGT
ENST00000697675.1:n.628_629delinsGT
ENST00000697676.1:n.205+412_205+413delinsGT
ENST00000697677.1:n.615_616delinsGT
ENST00000697678.1:n.47+568_47+569delinsGT
ENST00000697679.1:n.608_609delinsGT
ENST00000697680.1:c.*398_*399delinsGT	ENSP00000513392.1:n.*398_*399delinsGT
ENST00000697681.1:c.*398_*399delinsGT	ENSP00000513393.1:n.*398_*399delinsGT
ENST00000697683.1:c.*398_*399delinsGT	ENSP00000513395.1:n.*398_*399delinsGT
ENST00000697684.1:n.205+412_205+413delinsGT
ENST00000697685.1:c.*398_*399delinsGT	ENSP00000513396.1:n.*398_*399delinsGT
ENST00000697686.1:c.-207+568_-207+569delinsGT	ENSP00000513397.1:n.-207+568_-207+569delinsGT
ENST00000697687.1:n.191+412_191+413delinsGT
ENST00000697688.1:n.191+412_191+413delinsGT
ENST00000697689.1:c.*398_*399delinsGT	ENSP00000513398.1:n.*398_*399delinsGT
ENST00000697690.1:c.145+412_145+413delinsGT	ENSP00000513399.1:n.145+412_145+413delinsGT
ENST00000697691.1:c.43-151_43-150delinsGT	ENSP00000513400.1:n.43-151_43-150delinsGT
ENST00000697692.1:c.*157+241_*157+242delinsGT	ENSP00000513401.1:n.*157+241_*157+242delinsGT
ENST00000697693.1:n.470_471delinsGT
ENST00000697694.1:c.-207+82_-207+83delinsGT	ENSP00000513402.1:n.-207+82_-207+83delinsGT
ENST00000697695.1:n.274_275delinsGT
ENST00000337432.9:c.145+412_145+413delinsGT MANE Select	ENSP00000336701.4:n.145+412_145+413delinsGT
ENST00000337432.8:c.145+412_145+413delinsGT	ENSP00000336701.4:n.145+412_145+413delinsGT
ENST00000421782.3:c.145+412_145+413delinsGT	ENSP00000391450.2:n.145+412_145+413delinsGT
ENST00000461271.5:c.-207+515_-207+516delinsGT	ENSP00000464056.1:n.-207+515_-207+516delinsGT
ENST00000475762.5:c.*398_*399delinsGT	ENSP00000432421.1:n.*398_*399delinsGT
ENST00000476741.2:n.188-151_188-150delinsGT
ENST00000482007.5:c.145+412_145+413delinsGT	ENSP00000433332.1:n.145+412_145+413delinsGT
ENST00000486827.1:c.*398_*399delinsGT	ENSP00000436761.1:n.*398_*399delinsGT
ENST00000487525.5:c.145+412_145+413delinsGT	ENSP00000431637.1:n.145+412_145+413delinsGT
ENST00000487921.5:n.57+568_57+569delinsGT
ENST00000583539.5:c.145+412_145+413delinsGT	ENSP00000463121.1:n.145+412_145+413delinsGT
ENST00000584617.5:c.126+412_126+413delinsGT
NM_002876.3:c.145+412_145+413delinsGT	NP_002867.1:n.145+412_145+413delinsGT
NM_058216.2:c.145+412_145+413delinsGT	NP_478123.1:n.145+412_145+413delinsGT
NR_103872.1:n.216+412_216+413delinsGT
NR_103873.1:n.113+515_113+516delinsGT
XM_006722001.2:c.145+412_145+413delinsGT	XP_006722064.1:n.145+412_145+413delinsGT
XM_006722002.2:c.145+412_145+413delinsGT	XP_006722065.1:n.145+412_145+413delinsGT
XM_006722004.2:c.-207+515_-207+516delinsGT	XP_006722067.1:n.-207+515_-207+516delinsGT
XM_006722005.2:c.-207+568_-207+569delinsGT	XP_006722068.1:n.-207+568_-207+569delinsGT
XM_011525092.1:c.-506-151_-506-150delinsGT	XP_011523394.1:n.-506-151_-506-150delinsGT
XM_011525093.1:c.-667-151_-667-150delinsGT	XP_011523395.1:n.-667-151_-667-150delinsGT
XM_011525094.1:c.-207+241_-207+242delinsGT	XP_011523396.1:n.-207+241_-207+242delinsGT
XR_934513.1:n.218+412_218+413delinsGT
XR_934514.1:n.218+412_218+413delinsGT
XM_006722001.4:c.145+412_145+413delinsGT	XP_006722064.1:n.145+412_145+413delinsGT
XM_006722002.4:c.145+412_145+413delinsGT	XP_006722065.1:n.145+412_145+413delinsGT
XM_006722004.3:c.-207+515_-207+516delinsGT	XP_006722067.1:n.-207+515_-207+516delinsGT
XM_006722005.3:c.-207+568_-207+569delinsGT	XP_006722068.1:n.-207+568_-207+569delinsGT
XM_011525092.2:c.-506-151_-506-150delinsGT	XP_011523394.1:n.-506-151_-506-150delinsGT
XM_011525093.2:c.-667-151_-667-150delinsGT	XP_011523395.1:n.-667-151_-667-150delinsGT
XM_011525094.2:c.-207+241_-207+242delinsGT	XP_011523396.1:n.-207+241_-207+242delinsGT
XM_017024914.1:c.-207+515_-207+516delinsGT	XP_016880403.1:n.-207+515_-207+516delinsGT
XM_017024916.1:c.-506-151_-506-150delinsGT	XP_016880405.1:n.-506-151_-506-150delinsGT
XM_017024917.1:c.-207+568_-207+569delinsGT	XP_016880406.1:n.-207+568_-207+569delinsGT
XM_017024918.2:c.-207+241_-207+242delinsGT	XP_016880407.1:n.-207+241_-207+242delinsGT
XM_017024919.1:c.-667-151_-667-150delinsGT	XP_016880408.1:n.-667-151_-667-150delinsGT
XR_934513.3:n.649+412_649+413delinsGT
XR_934514.3:n.649+412_649+413delinsGT
NM_058216.3:c.145+412_145+413delinsGT MANE Select	NP_478123.1:n.145+412_145+413delinsGT
NR_103872.2:n.187+412_187+413delinsGT
NM_002876.4:c.145+412_145+413delinsGT	NP_002867.1:n.145+412_145+413delinsGT