Canonical Allele Identifier: CA2267814319

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58693145_58693146delinsGA , CM000679.2:g.58693145_58693146delinsGA	GRCh38
NC_000017.10:g.56770506_56770507delinsGA , CM000679.1:g.56770506_56770507delinsGA	GRCh37
NC_000017.9:g.54125505_54125506delinsGA	NCBI36
NG_023199.1:g.5544_5545delinsGA , LRG_314:g.5544_5545delinsGA
NG_047169.1:g.3934_3935delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-207+460_-207+461delinsGA	ENSP00000464056.2:n.-207+460_-207+461delinsGA
ENST00000697675.1:n.573_574delinsGA
ENST00000697676.1:n.205+357_205+358delinsGA
ENST00000697677.1:n.560_561delinsGA
ENST00000697678.1:n.47+513_47+514delinsGA
ENST00000697679.1:n.553_554delinsGA
ENST00000697680.1:c.*343_*344delinsGA	ENSP00000513392.1:n.*343_*344delinsGA
ENST00000697681.1:c.*343_*344delinsGA	ENSP00000513393.1:n.*343_*344delinsGA
ENST00000697683.1:c.*343_*344delinsGA	ENSP00000513395.1:n.*343_*344delinsGA
ENST00000697684.1:n.205+357_205+358delinsGA
ENST00000697685.1:c.*343_*344delinsGA	ENSP00000513396.1:n.*343_*344delinsGA
ENST00000697686.1:c.-207+513_-207+514delinsGA	ENSP00000513397.1:n.-207+513_-207+514delinsGA
ENST00000697687.1:n.191+357_191+358delinsGA
ENST00000697688.1:n.191+357_191+358delinsGA
ENST00000697689.1:c.*343_*344delinsGA	ENSP00000513398.1:n.*343_*344delinsGA
ENST00000697690.1:c.145+357_145+358delinsGA	ENSP00000513399.1:n.145+357_145+358delinsGA
ENST00000697691.1:c.43-206_43-205delinsGA	ENSP00000513400.1:n.43-206_43-205delinsGA
ENST00000697692.1:c.*157+186_*157+187delinsGA	ENSP00000513401.1:n.*157+186_*157+187delinsGA
ENST00000697693.1:n.415_416delinsGA
ENST00000697694.1:c.-207+27_-207+28delinsGA	ENSP00000513402.1:n.-207+27_-207+28delinsGA
ENST00000697695.1:n.219_220delinsGA
ENST00000337432.9:c.145+357_145+358delinsGA MANE Select	ENSP00000336701.4:n.145+357_145+358delinsGA
ENST00000337432.8:c.145+357_145+358delinsGA	ENSP00000336701.4:n.145+357_145+358delinsGA
ENST00000421782.3:c.145+357_145+358delinsGA	ENSP00000391450.2:n.145+357_145+358delinsGA
ENST00000461271.5:c.-207+460_-207+461delinsGA	ENSP00000464056.1:n.-207+460_-207+461delinsGA
ENST00000475762.5:c.*343_*344delinsGA	ENSP00000432421.1:n.*343_*344delinsGA
ENST00000476741.2:n.188-206_188-205delinsGA
ENST00000482007.5:c.145+357_145+358delinsGA	ENSP00000433332.1:n.145+357_145+358delinsGA
ENST00000486827.1:c.*343_*344delinsGA	ENSP00000436761.1:n.*343_*344delinsGA
ENST00000487525.5:c.145+357_145+358delinsGA	ENSP00000431637.1:n.145+357_145+358delinsGA
ENST00000487921.5:n.57+513_57+514delinsGA
ENST00000583539.5:c.145+357_145+358delinsGA	ENSP00000463121.1:n.145+357_145+358delinsGA
ENST00000584617.5:c.126+357_126+358delinsGA
NM_002876.3:c.145+357_145+358delinsGA	NP_002867.1:n.145+357_145+358delinsGA
NM_058216.2:c.145+357_145+358delinsGA	NP_478123.1:n.145+357_145+358delinsGA
NR_103872.1:n.216+357_216+358delinsGA
NR_103873.1:n.113+460_113+461delinsGA
XM_006722001.2:c.145+357_145+358delinsGA	XP_006722064.1:n.145+357_145+358delinsGA
XM_006722002.2:c.145+357_145+358delinsGA	XP_006722065.1:n.145+357_145+358delinsGA
XM_006722004.2:c.-207+460_-207+461delinsGA	XP_006722067.1:n.-207+460_-207+461delinsGA
XM_006722005.2:c.-207+513_-207+514delinsGA	XP_006722068.1:n.-207+513_-207+514delinsGA
XM_011525092.1:c.-506-206_-506-205delinsGA	XP_011523394.1:n.-506-206_-506-205delinsGA
XM_011525093.1:c.-667-206_-667-205delinsGA	XP_011523395.1:n.-667-206_-667-205delinsGA
XM_011525094.1:c.-207+186_-207+187delinsGA	XP_011523396.1:n.-207+186_-207+187delinsGA
XR_934513.1:n.218+357_218+358delinsGA
XR_934514.1:n.218+357_218+358delinsGA
XM_006722001.4:c.145+357_145+358delinsGA	XP_006722064.1:n.145+357_145+358delinsGA
XM_006722002.4:c.145+357_145+358delinsGA	XP_006722065.1:n.145+357_145+358delinsGA
XM_006722004.3:c.-207+460_-207+461delinsGA	XP_006722067.1:n.-207+460_-207+461delinsGA
XM_006722005.3:c.-207+513_-207+514delinsGA	XP_006722068.1:n.-207+513_-207+514delinsGA
XM_011525092.2:c.-506-206_-506-205delinsGA	XP_011523394.1:n.-506-206_-506-205delinsGA
XM_011525093.2:c.-667-206_-667-205delinsGA	XP_011523395.1:n.-667-206_-667-205delinsGA
XM_011525094.2:c.-207+186_-207+187delinsGA	XP_011523396.1:n.-207+186_-207+187delinsGA
XM_017024914.1:c.-207+460_-207+461delinsGA	XP_016880403.1:n.-207+460_-207+461delinsGA
XM_017024916.1:c.-506-206_-506-205delinsGA	XP_016880405.1:n.-506-206_-506-205delinsGA
XM_017024917.1:c.-207+513_-207+514delinsGA	XP_016880406.1:n.-207+513_-207+514delinsGA
XM_017024918.2:c.-207+186_-207+187delinsGA	XP_016880407.1:n.-207+186_-207+187delinsGA
XM_017024919.1:c.-667-206_-667-205delinsGA	XP_016880408.1:n.-667-206_-667-205delinsGA
XR_934513.3:n.649+357_649+358delinsGA
XR_934514.3:n.649+357_649+358delinsGA
NM_058216.3:c.145+357_145+358delinsGA MANE Select	NP_478123.1:n.145+357_145+358delinsGA
NR_103872.2:n.187+357_187+358delinsGA
NM_002876.4:c.145+357_145+358delinsGA	NP_002867.1:n.145+357_145+358delinsGA