Canonical Allele Identifier: CA2576336283

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692792del , CM000679.2:g.58692792del	GRCh38
NC_000017.10:g.56770153del , CM000679.1:g.56770153del	GRCh37
NC_000017.9:g.54125152del	NCBI36
NG_023199.1:g.5191del , LRG_314:g.5191del
NG_047169.1:g.4289del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-207+107del	ENSP00000464056.2:n.-207+107del
ENST00000697675.1:n.220del
ENST00000697676.1:n.205+4del
ENST00000697677.1:n.207del
ENST00000697678.1:n.47+160del
ENST00000697679.1:n.200del
ENST00000697680.1:c.149del	ENSP00000513392.1:p.Asn50ThrfsTer?
ENST00000697681.1:c.149del	ENSP00000513393.1:p.Asn50ThrfsTer?
ENST00000697683.1:c.149del	ENSP00000513395.1:p.Asn50ThrfsTer?
ENST00000697684.1:n.205+4del
ENST00000697685.1:c.149del	ENSP00000513396.1:p.Asn50ThrfsTer?
ENST00000697686.1:c.-207+160del	ENSP00000513397.1:n.-207+160del
ENST00000697687.1:n.191+4del
ENST00000697688.1:n.191+4del
ENST00000697689.1:c.149del	ENSP00000513398.1:p.Asn50ThrfsTer?
ENST00000697690.1:c.145+4del	ENSP00000513399.1:n.145+4del
ENST00000697691.1:c.42+107del	ENSP00000513400.1:n.42+107del
ENST00000697692.1:c.149del	ENSP00000513401.1:p.Asn50ThrfsTer?
ENST00000697693.1:n.62del
ENST00000337432.9:c.145+4del MANE Select	ENSP00000336701.4:n.145+4del
ENST00000337432.8:c.145+4del	ENSP00000336701.4:n.145+4del
ENST00000421782.3:c.145+4del	ENSP00000391450.2:n.145+4del
ENST00000461271.5:c.-207+107del	ENSP00000464056.1:n.-207+107del
ENST00000475762.5:c.149del	ENSP00000432421.1:p.Asn50ThrfsTer?
ENST00000476741.2:n.187+4del
ENST00000482007.5:c.145+4del	ENSP00000433332.1:n.145+4del
ENST00000486827.1:c.149del	ENSP00000436761.1:p.Asn50ThrfsTer?
ENST00000487525.5:c.145+4del	ENSP00000431637.1:n.145+4del
ENST00000487921.5:n.57+160del
ENST00000583539.5:c.145+4del	ENSP00000463121.1:n.145+4del
ENST00000584617.5:c.126+4del
NM_002876.3:c.145+4del	NP_002867.1:n.145+4del
NM_058216.2:c.145+4del	NP_478123.1:n.145+4del
NR_103872.1:n.216+4del
NR_103873.1:n.113+107del
XM_006722001.2:c.145+4del	XP_006722064.1:n.145+4del
XM_006722002.2:c.145+4del	XP_006722065.1:n.145+4del
XM_006722004.2:c.-207+107del	XP_006722067.1:n.-207+107del
XM_006722005.2:c.-207+160del	XP_006722068.1:n.-207+160del
XM_011525092.1:c.-507+107del	XP_011523394.1:n.-507+107del
XM_011525093.1:c.-668+107del	XP_011523395.1:n.-668+107del
XR_934513.1:n.218+4del
XR_934514.1:n.218+4del
XM_006722001.4:c.145+4del	XP_006722064.1:n.145+4del
XM_006722002.4:c.145+4del	XP_006722065.1:n.145+4del
XM_006722004.3:c.-207+107del	XP_006722067.1:n.-207+107del
XM_006722005.3:c.-207+160del	XP_006722068.1:n.-207+160del
XM_011525092.2:c.-507+107del	XP_011523394.1:n.-507+107del
XM_011525093.2:c.-668+107del	XP_011523395.1:n.-668+107del
XM_017024914.1:c.-207+107del	XP_016880403.1:n.-207+107del
XM_017024916.1:c.-507+107del	XP_016880405.1:n.-507+107del
XM_017024917.1:c.-207+160del	XP_016880406.1:n.-207+160del
XM_017024918.2:c.-374del	XP_016880407.1:n.-374del
XM_017024919.1:c.-668+107del	XP_016880408.1:n.-668+107del
XR_934513.3:n.649+4del
XR_934514.3:n.649+4del
NM_058216.3:c.145+4del MANE Select	NP_478123.1:n.145+4del
NR_103872.2:n.187+4del
NM_002876.4:c.145+4del	NP_002867.1:n.145+4del