Canonical Allele Identifier: CA2267814281

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58693075_58693076delinsTA , CM000679.2:g.58693075_58693076delinsTA	GRCh38
NC_000017.10:g.56770436_56770437delinsTA , CM000679.1:g.56770436_56770437delinsTA	GRCh37
NC_000017.9:g.54125435_54125436delinsTA	NCBI36
NG_023199.1:g.5474_5475delinsTA , LRG_314:g.5474_5475delinsTA
NG_047169.1:g.4004_4005delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-207+390_-207+391delinsTA	ENSP00000464056.2:n.-207+390_-207+391delinsTA
ENST00000697675.1:n.503_504delinsTA
ENST00000697676.1:n.205+287_205+288delinsTA
ENST00000697677.1:n.490_491delinsTA
ENST00000697678.1:n.47+443_47+444delinsTA
ENST00000697679.1:n.483_484delinsTA
ENST00000697680.1:c.*273_*274delinsTA	ENSP00000513392.1:n.*273_*274delinsTA
ENST00000697681.1:c.*273_*274delinsTA	ENSP00000513393.1:n.*273_*274delinsTA
ENST00000697683.1:c.*273_*274delinsTA	ENSP00000513395.1:n.*273_*274delinsTA
ENST00000697684.1:n.205+287_205+288delinsTA
ENST00000697685.1:c.*273_*274delinsTA	ENSP00000513396.1:n.*273_*274delinsTA
ENST00000697686.1:c.-207+443_-207+444delinsTA	ENSP00000513397.1:n.-207+443_-207+444delinsTA
ENST00000697687.1:n.191+287_191+288delinsTA
ENST00000697688.1:n.191+287_191+288delinsTA
ENST00000697689.1:c.*273_*274delinsTA	ENSP00000513398.1:n.*273_*274delinsTA
ENST00000697690.1:c.145+287_145+288delinsTA	ENSP00000513399.1:n.145+287_145+288delinsTA
ENST00000697691.1:c.43-276_43-275delinsTA	ENSP00000513400.1:n.43-276_43-275delinsTA
ENST00000697692.1:c.*157+116_*157+117delinsTA	ENSP00000513401.1:n.*157+116_*157+117delinsTA
ENST00000697693.1:n.345_346delinsTA
ENST00000697694.1:c.-250_-249delinsTA	ENSP00000513402.1:n.-250_-249delinsTA
ENST00000697695.1:n.149_150delinsTA
ENST00000337432.9:c.145+287_145+288delinsTA MANE Select	ENSP00000336701.4:n.145+287_145+288delinsTA
ENST00000337432.8:c.145+287_145+288delinsTA	ENSP00000336701.4:n.145+287_145+288delinsTA
ENST00000421782.3:c.145+287_145+288delinsTA	ENSP00000391450.2:n.145+287_145+288delinsTA
ENST00000461271.5:c.-207+390_-207+391delinsTA	ENSP00000464056.1:n.-207+390_-207+391delinsTA
ENST00000475762.5:c.*273_*274delinsTA	ENSP00000432421.1:n.*273_*274delinsTA
ENST00000476741.2:n.188-276_188-275delinsTA
ENST00000482007.5:c.145+287_145+288delinsTA	ENSP00000433332.1:n.145+287_145+288delinsTA
ENST00000486827.1:c.*273_*274delinsTA	ENSP00000436761.1:n.*273_*274delinsTA
ENST00000487525.5:c.145+287_145+288delinsTA	ENSP00000431637.1:n.145+287_145+288delinsTA
ENST00000487921.5:n.57+443_57+444delinsTA
ENST00000583539.5:c.145+287_145+288delinsTA	ENSP00000463121.1:n.145+287_145+288delinsTA
ENST00000584617.5:c.126+287_126+288delinsTA
NM_002876.3:c.145+287_145+288delinsTA	NP_002867.1:n.145+287_145+288delinsTA
NM_058216.2:c.145+287_145+288delinsTA	NP_478123.1:n.145+287_145+288delinsTA
NR_103872.1:n.216+287_216+288delinsTA
NR_103873.1:n.113+390_113+391delinsTA
XM_006722001.2:c.145+287_145+288delinsTA	XP_006722064.1:n.145+287_145+288delinsTA
XM_006722002.2:c.145+287_145+288delinsTA	XP_006722065.1:n.145+287_145+288delinsTA
XM_006722004.2:c.-207+390_-207+391delinsTA	XP_006722067.1:n.-207+390_-207+391delinsTA
XM_006722005.2:c.-207+443_-207+444delinsTA	XP_006722068.1:n.-207+443_-207+444delinsTA
XM_011525092.1:c.-506-276_-506-275delinsTA	XP_011523394.1:n.-506-276_-506-275delinsTA
XM_011525093.1:c.-667-276_-667-275delinsTA	XP_011523395.1:n.-667-276_-667-275delinsTA
XM_011525094.1:c.-207+116_-207+117delinsTA	XP_011523396.1:n.-207+116_-207+117delinsTA
XR_934513.1:n.218+287_218+288delinsTA
XR_934514.1:n.218+287_218+288delinsTA
XM_006722001.4:c.145+287_145+288delinsTA	XP_006722064.1:n.145+287_145+288delinsTA
XM_006722002.4:c.145+287_145+288delinsTA	XP_006722065.1:n.145+287_145+288delinsTA
XM_006722004.3:c.-207+390_-207+391delinsTA	XP_006722067.1:n.-207+390_-207+391delinsTA
XM_006722005.3:c.-207+443_-207+444delinsTA	XP_006722068.1:n.-207+443_-207+444delinsTA
XM_011525092.2:c.-506-276_-506-275delinsTA	XP_011523394.1:n.-506-276_-506-275delinsTA
XM_011525093.2:c.-667-276_-667-275delinsTA	XP_011523395.1:n.-667-276_-667-275delinsTA
XM_011525094.2:c.-207+116_-207+117delinsTA	XP_011523396.1:n.-207+116_-207+117delinsTA
XM_017024914.1:c.-207+390_-207+391delinsTA	XP_016880403.1:n.-207+390_-207+391delinsTA
XM_017024916.1:c.-506-276_-506-275delinsTA	XP_016880405.1:n.-506-276_-506-275delinsTA
XM_017024917.1:c.-207+443_-207+444delinsTA	XP_016880406.1:n.-207+443_-207+444delinsTA
XM_017024918.2:c.-207+116_-207+117delinsTA	XP_016880407.1:n.-207+116_-207+117delinsTA
XM_017024919.1:c.-667-276_-667-275delinsTA	XP_016880408.1:n.-667-276_-667-275delinsTA
XR_934513.3:n.649+287_649+288delinsTA
XR_934514.3:n.649+287_649+288delinsTA
NM_058216.3:c.145+287_145+288delinsTA MANE Select	NP_478123.1:n.145+287_145+288delinsTA
NR_103872.2:n.187+287_187+288delinsTA
NM_002876.4:c.145+287_145+288delinsTA	NP_002867.1:n.145+287_145+288delinsTA