Canonical Allele Identifier: CA2267814095

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692789_58692795delinsGTAACGA , CM000679.2:g.58692789_58692795delinsGTAACGA	GRCh38
NC_000017.10:g.56770150_56770156delinsGTAACGA , CM000679.1:g.56770150_56770156delinsGTAACGA	GRCh37
NC_000017.9:g.54125149_54125155delinsGTAACGA	NCBI36
NG_023199.1:g.5188_5194delinsGTAACGA , LRG_314:g.5188_5194delinsGTAACGA
NG_047169.1:g.4285_4291delinsTCGTTAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.-207+104_-207+110delinsGTAACGA	ENSP00000464056.2:n.-207+104_-207+110delinsGTAACGA
ENST00000697675.1:n.217_223delinsGTAACGA
ENST00000697676.1:n.205+1_205+7delinsGTAACGA
ENST00000697677.1:n.204_210delinsGTAACGA
ENST00000697678.1:n.47+157_47+163delinsGTAACGA
ENST00000697679.1:n.197_203delinsGTAACGA
ENST00000697680.1:c.146_152delinsGTAACGA	ENSP00000513392.1:p.Gly49=
ENST00000697681.1:c.146_152delinsGTAACGA	ENSP00000513393.1:p.Gly49=
ENST00000697683.1:c.146_152delinsGTAACGA	ENSP00000513395.1:p.Gly49=
ENST00000697684.1:n.205+1_205+7delinsGTAACGA
ENST00000697685.1:c.146_152delinsGTAACGA	ENSP00000513396.1:p.Gly49=
ENST00000697686.1:c.-207+157_-207+163delinsGTAACGA	ENSP00000513397.1:n.-207+157_-207+163delinsGTAACGA
ENST00000697687.1:n.191+1_191+7delinsGTAACGA
ENST00000697688.1:n.191+1_191+7delinsGTAACGA
ENST00000697689.1:c.146_152delinsGTAACGA	ENSP00000513398.1:p.Gly49=
ENST00000697690.1:c.145+1_145+7delinsGTAACGA	ENSP00000513399.1:n.145+1_145+7delinsGTAACGA
ENST00000697691.1:c.42+104_42+110delinsGTAACGA	ENSP00000513400.1:n.42+104_42+110delinsGTAACGA
ENST00000697692.1:c.146_152delinsGTAACGA	ENSP00000513401.1:p.Gly49=
ENST00000697693.1:n.59_65delinsGTAACGA
ENST00000337432.9:c.145+1_145+7delinsGTAACGA MANE Select	ENSP00000336701.4:n.145+1_145+7delinsGTAACGA
ENST00000337432.8:c.145+1_145+7delinsGTAACGA	ENSP00000336701.4:n.145+1_145+7delinsGTAACGA
ENST00000421782.3:c.145+1_145+7delinsGTAACGA	ENSP00000391450.2:n.145+1_145+7delinsGTAACGA
ENST00000461271.5:c.-207+104_-207+110delinsGTAACGA	ENSP00000464056.1:n.-207+104_-207+110delinsGTAACGA
ENST00000475762.5:c.146_152delinsGTAACGA	ENSP00000432421.1:p.Gly49=
ENST00000476741.2:n.187+1_187+7delinsGTAACGA
ENST00000482007.5:c.145+1_145+7delinsGTAACGA	ENSP00000433332.1:n.145+1_145+7delinsGTAACGA
ENST00000486827.1:c.146_152delinsGTAACGA	ENSP00000436761.1:p.Gly49=
ENST00000487525.5:c.145+1_145+7delinsGTAACGA	ENSP00000431637.1:n.145+1_145+7delinsGTAACGA
ENST00000487921.5:n.57+157_57+163delinsGTAACGA
ENST00000583539.5:c.145+1_145+7delinsGTAACGA	ENSP00000463121.1:n.145+1_145+7delinsGTAACGA
ENST00000584617.5:c.126+1_126+7delinsGTAACGA
NM_002876.3:c.145+1_145+7delinsGTAACGA	NP_002867.1:n.145+1_145+7delinsGTAACGA
NM_058216.2:c.145+1_145+7delinsGTAACGA	NP_478123.1:n.145+1_145+7delinsGTAACGA
NR_103872.1:n.216+1_216+7delinsGTAACGA
NR_103873.1:n.113+104_113+110delinsGTAACGA
XM_006722001.2:c.145+1_145+7delinsGTAACGA	XP_006722064.1:n.145+1_145+7delinsGTAACGA
XM_006722002.2:c.145+1_145+7delinsGTAACGA	XP_006722065.1:n.145+1_145+7delinsGTAACGA
XM_006722004.2:c.-207+104_-207+110delinsGTAACGA	XP_006722067.1:n.-207+104_-207+110delinsGTAACGA
XM_006722005.2:c.-207+157_-207+163delinsGTAACGA	XP_006722068.1:n.-207+157_-207+163delinsGTAACGA
XM_011525092.1:c.-507+104_-507+110delinsGTAACGA	XP_011523394.1:n.-507+104_-507+110delinsGTAACGA
XM_011525093.1:c.-668+104_-668+110delinsGTAACGA	XP_011523395.1:n.-668+104_-668+110delinsGTAACGA
XR_934513.1:n.218+1_218+7delinsGTAACGA
XR_934514.1:n.218+1_218+7delinsGTAACGA
XM_006722001.4:c.145+1_145+7delinsGTAACGA	XP_006722064.1:n.145+1_145+7delinsGTAACGA
XM_006722002.4:c.145+1_145+7delinsGTAACGA	XP_006722065.1:n.145+1_145+7delinsGTAACGA
XM_006722004.3:c.-207+104_-207+110delinsGTAACGA	XP_006722067.1:n.-207+104_-207+110delinsGTAACGA
XM_006722005.3:c.-207+157_-207+163delinsGTAACGA	XP_006722068.1:n.-207+157_-207+163delinsGTAACGA
XM_011525092.2:c.-507+104_-507+110delinsGTAACGA	XP_011523394.1:n.-507+104_-507+110delinsGTAACGA
XM_011525093.2:c.-668+104_-668+110delinsGTAACGA	XP_011523395.1:n.-668+104_-668+110delinsGTAACGA
XM_017024914.1:c.-207+104_-207+110delinsGTAACGA	XP_016880403.1:n.-207+104_-207+110delinsGTAACGA
XM_017024916.1:c.-507+104_-507+110delinsGTAACGA	XP_016880405.1:n.-507+104_-507+110delinsGTAACGA
XM_017024917.1:c.-207+157_-207+163delinsGTAACGA	XP_016880406.1:n.-207+157_-207+163delinsGTAACGA
XM_017024918.2:c.-377_-371delinsGTAACGA	XP_016880407.1:n.-377_-371delinsGTAACGA
XM_017024919.1:c.-668+104_-668+110delinsGTAACGA	XP_016880408.1:n.-668+104_-668+110delinsGTAACGA
XR_934513.3:n.649+1_649+7delinsGTAACGA
XR_934514.3:n.649+1_649+7delinsGTAACGA
NM_058216.3:c.145+1_145+7delinsGTAACGA MANE Select	NP_478123.1:n.145+1_145+7delinsGTAACGA
NR_103872.2:n.187+1_187+7delinsGTAACGA
NM_002876.4:c.145+1_145+7delinsGTAACGA	NP_002867.1:n.145+1_145+7delinsGTAACGA