Canonical Allele Identifier: CA3060596512

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692801_58692802del , CM000679.2:g.58692801_58692802del	GRCh38
NC_000017.10:g.56770162_56770163del , CM000679.1:g.56770162_56770163del	GRCh37
NC_000017.9:g.54125161_54125162del	NCBI36
NG_023199.1:g.5200_5201del , LRG_314:g.5200_5201del
NG_047169.1:g.4278_4279del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-207+116_-207+117del	ENSP00000464056.2:n.-207+116_-207+117del
ENST00000697675.1:n.229_230del
ENST00000697676.1:n.205+13_205+14del
ENST00000697677.1:n.216_217del
ENST00000697678.1:n.47+169_47+170del
ENST00000697679.1:n.209_210del
ENST00000697680.1:c.158_159del	ENSP00000513392.1:p.Ter53LeuextTer4
ENST00000697681.1:c.158_159del	ENSP00000513393.1:p.Ter53LeuextTer4
ENST00000697683.1:c.158_159del	ENSP00000513395.1:p.Ter53LeuextTer4
ENST00000697684.1:n.205+13_205+14del
ENST00000697685.1:c.158_159del	ENSP00000513396.1:p.Ter53LeuextTer4
ENST00000697686.1:c.-207+169_-207+170del	ENSP00000513397.1:n.-207+169_-207+170del
ENST00000697687.1:n.191+13_191+14del
ENST00000697688.1:n.191+13_191+14del
ENST00000697689.1:c.158_159del	ENSP00000513398.1:p.Ter53LeuextTer4
ENST00000697690.1:c.145+13_145+14del	ENSP00000513399.1:n.145+13_145+14del
ENST00000697691.1:c.42+116_42+117del	ENSP00000513400.1:n.42+116_42+117del
ENST00000697692.1:c.158_159del	ENSP00000513401.1:p.Ter53LeuextTer4
ENST00000697693.1:n.71_72del
ENST00000337432.9:c.145+13_145+14del MANE Select	ENSP00000336701.4:n.145+13_145+14del
ENST00000337432.8:c.145+13_145+14del	ENSP00000336701.4:n.145+13_145+14del
ENST00000421782.3:c.145+13_145+14del	ENSP00000391450.2:n.145+13_145+14del
ENST00000461271.5:c.-207+116_-207+117del	ENSP00000464056.1:n.-207+116_-207+117del
ENST00000475762.5:c.158_159del	ENSP00000432421.1:p.Ter53LeuextTer4
ENST00000476741.2:n.187+13_187+14del
ENST00000482007.5:c.145+13_145+14del	ENSP00000433332.1:n.145+13_145+14del
ENST00000486827.1:c.158_159del	ENSP00000436761.1:p.Ter53LeuextTer4
ENST00000487525.5:c.145+13_145+14del	ENSP00000431637.1:n.145+13_145+14del
ENST00000487921.5:n.57+169_57+170del
ENST00000583539.5:c.145+13_145+14del	ENSP00000463121.1:n.145+13_145+14del
ENST00000584617.5:c.126+13_126+14del
NM_002876.3:c.145+13_145+14del	NP_002867.1:n.145+13_145+14del
NM_058216.2:c.145+13_145+14del	NP_478123.1:n.145+13_145+14del
NR_103872.1:n.216+13_216+14del
NR_103873.1:n.113+116_113+117del
XM_006722001.2:c.145+13_145+14del	XP_006722064.1:n.145+13_145+14del
XM_006722002.2:c.145+13_145+14del	XP_006722065.1:n.145+13_145+14del
XM_006722004.2:c.-207+116_-207+117del	XP_006722067.1:n.-207+116_-207+117del
XM_006722005.2:c.-207+169_-207+170del	XP_006722068.1:n.-207+169_-207+170del
XM_011525092.1:c.-507+116_-507+117del	XP_011523394.1:n.-507+116_-507+117del
XM_011525093.1:c.-668+116_-668+117del	XP_011523395.1:n.-668+116_-668+117del
XR_934513.1:n.218+13_218+14del
XR_934514.1:n.218+13_218+14del
XM_006722001.4:c.145+13_145+14del	XP_006722064.1:n.145+13_145+14del
XM_006722002.4:c.145+13_145+14del	XP_006722065.1:n.145+13_145+14del
XM_006722004.3:c.-207+116_-207+117del	XP_006722067.1:n.-207+116_-207+117del
XM_006722005.3:c.-207+169_-207+170del	XP_006722068.1:n.-207+169_-207+170del
XM_011525092.2:c.-507+116_-507+117del	XP_011523394.1:n.-507+116_-507+117del
XM_011525093.2:c.-668+116_-668+117del	XP_011523395.1:n.-668+116_-668+117del
XM_011525094.2:c.-365_-364del	XP_011523396.1:n.-365_-364del
XM_017024914.1:c.-207+116_-207+117del	XP_016880403.1:n.-207+116_-207+117del
XM_017024916.1:c.-507+116_-507+117del	XP_016880405.1:n.-507+116_-507+117del
XM_017024917.1:c.-207+169_-207+170del	XP_016880406.1:n.-207+169_-207+170del
XM_017024918.2:c.-365_-364del	XP_016880407.1:n.-365_-364del
XM_017024919.1:c.-668+116_-668+117del	XP_016880408.1:n.-668+116_-668+117del
XR_934513.3:n.649+13_649+14del
XR_934514.3:n.649+13_649+14del
NM_058216.3:c.145+13_145+14del MANE Select	NP_478123.1:n.145+13_145+14del
NR_103872.2:n.187+13_187+14del
NM_002876.4:c.145+13_145+14del	NP_002867.1:n.145+13_145+14del