Canonical Allele Identifier: CA2809980379

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692878_58692881del , CM000679.2:g.58692878_58692881del	GRCh38
NC_000017.10:g.56770239_56770242del , CM000679.1:g.56770239_56770242del	GRCh37
NC_000017.9:g.54125238_54125241del	NCBI36
NG_023199.1:g.5277_5280del , LRG_314:g.5277_5280del
NG_047169.1:g.4199_4202del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-207+193_-207+196del	ENSP00000464056.2:n.-207+193_-207+196del
ENST00000697675.1:n.306_309del
ENST00000697676.1:n.205+90_205+93del
ENST00000697677.1:n.293_296del
ENST00000697678.1:n.47+246_47+249del
ENST00000697679.1:n.286_289del
ENST00000697680.1:c.*76_*79del	ENSP00000513392.1:n.*76_*79del
ENST00000697681.1:c.*76_*79del	ENSP00000513393.1:n.*76_*79del
ENST00000697683.1:c.*76_*79del	ENSP00000513395.1:n.*76_*79del
ENST00000697684.1:n.205+90_205+93del
ENST00000697685.1:c.*76_*79del	ENSP00000513396.1:n.*76_*79del
ENST00000697686.1:c.-207+246_-207+249del	ENSP00000513397.1:n.-207+246_-207+249del
ENST00000697687.1:n.191+90_191+93del
ENST00000697688.1:n.191+90_191+93del
ENST00000697689.1:c.*76_*79del	ENSP00000513398.1:n.*76_*79del
ENST00000697690.1:c.145+90_145+93del	ENSP00000513399.1:n.145+90_145+93del
ENST00000697691.1:c.42+193_42+196del	ENSP00000513400.1:n.42+193_42+196del
ENST00000697692.1:c.*76_*79del	ENSP00000513401.1:n.*76_*79del
ENST00000697693.1:n.148_151del
ENST00000337432.9:c.145+90_145+93del MANE Select	ENSP00000336701.4:n.145+90_145+93del
ENST00000337432.8:c.145+90_145+93del	ENSP00000336701.4:n.145+90_145+93del
ENST00000421782.3:c.145+90_145+93del	ENSP00000391450.2:n.145+90_145+93del
ENST00000461271.5:c.-207+193_-207+196del	ENSP00000464056.1:n.-207+193_-207+196del
ENST00000475762.5:c.*76_*79del	ENSP00000432421.1:n.*76_*79del
ENST00000476741.2:n.187+90_187+93del
ENST00000482007.5:c.145+90_145+93del	ENSP00000433332.1:n.145+90_145+93del
ENST00000486827.1:c.*76_*79del	ENSP00000436761.1:n.*76_*79del
ENST00000487525.5:c.145+90_145+93del	ENSP00000431637.1:n.145+90_145+93del
ENST00000487921.5:n.57+246_57+249del
ENST00000583539.5:c.145+90_145+93del	ENSP00000463121.1:n.145+90_145+93del
ENST00000584617.5:c.126+90_126+93del
NM_002876.3:c.145+90_145+93del	NP_002867.1:n.145+90_145+93del
NM_058216.2:c.145+90_145+93del	NP_478123.1:n.145+90_145+93del
NR_103872.1:n.216+90_216+93del
NR_103873.1:n.113+193_113+196del
XM_006722001.2:c.145+90_145+93del	XP_006722064.1:n.145+90_145+93del
XM_006722002.2:c.145+90_145+93del	XP_006722065.1:n.145+90_145+93del
XM_006722004.2:c.-207+193_-207+196del	XP_006722067.1:n.-207+193_-207+196del
XM_006722005.2:c.-207+246_-207+249del	XP_006722068.1:n.-207+246_-207+249del
XM_011525092.1:c.-507+193_-507+196del	XP_011523394.1:n.-507+193_-507+196del
XM_011525093.1:c.-668+193_-668+196del	XP_011523395.1:n.-668+193_-668+196del
XM_011525094.1:c.-288_-285del	XP_011523396.1:n.-288_-285del
XR_934513.1:n.218+90_218+93del
XR_934514.1:n.218+90_218+93del
XM_006722001.4:c.145+90_145+93del	XP_006722064.1:n.145+90_145+93del
XM_006722002.4:c.145+90_145+93del	XP_006722065.1:n.145+90_145+93del
XM_006722004.3:c.-207+193_-207+196del	XP_006722067.1:n.-207+193_-207+196del
XM_006722005.3:c.-207+246_-207+249del	XP_006722068.1:n.-207+246_-207+249del
XM_011525092.2:c.-507+193_-507+196del	XP_011523394.1:n.-507+193_-507+196del
XM_011525093.2:c.-668+193_-668+196del	XP_011523395.1:n.-668+193_-668+196del
XM_011525094.2:c.-288_-285del	XP_011523396.1:n.-288_-285del
XM_017024914.1:c.-207+193_-207+196del	XP_016880403.1:n.-207+193_-207+196del
XM_017024916.1:c.-507+193_-507+196del	XP_016880405.1:n.-507+193_-507+196del
XM_017024917.1:c.-207+246_-207+249del	XP_016880406.1:n.-207+246_-207+249del
XM_017024918.2:c.-288_-285del	XP_016880407.1:n.-288_-285del
XM_017024919.1:c.-668+193_-668+196del	XP_016880408.1:n.-668+193_-668+196del
XR_934513.3:n.649+90_649+93del
XR_934514.3:n.649+90_649+93del
NM_058216.3:c.145+90_145+93del MANE Select	NP_478123.1:n.145+90_145+93del
NR_103872.2:n.187+90_187+93del
NM_002876.4:c.145+90_145+93del	NP_002867.1:n.145+90_145+93del