Canonical Allele Identifier: CA3057242744

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58709924_58709926delinsGCC , CM000679.2:g.58709924_58709926delinsGCC	GRCh38
NC_000017.10:g.56787285_56787287delinsGCC , CM000679.1:g.56787285_56787287delinsGCC	GRCh37
NC_000017.9:g.54142284_54142286delinsGCC	NCBI36
NG_023199.1:g.22323_22325delinsGCC , LRG_314:g.22323_22325delinsGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.420_422delinsGCC	ENSP00000464056.2:p.Arg141Pro
ENST00000697678.1:n.673_675delinsGCC
ENST00000697679.1:n.1845_1847delinsGCC
ENST00000697680.1:c.*1635_*1637delinsGCC	ENSP00000513392.1:n.*1635_*1637delinsGCC
ENST00000697681.1:c.*1932_*1934delinsGCC	ENSP00000513393.1:n.*1932_*1934delinsGCC
ENST00000697683.1:c.*1635_*1637delinsGCC	ENSP00000513395.1:n.*1635_*1637delinsGCC
ENST00000697684.1:n.831_833delinsGCC
ENST00000697685.1:c.*1468_*1470delinsGCC	ENSP00000513396.1:n.*1468_*1470delinsGCC
ENST00000697686.1:c.420_422delinsGCC	ENSP00000513397.1:p.Arg141Pro
ENST00000697687.1:n.650_652delinsGCC
ENST00000697688.1:n.817_819delinsGCC
ENST00000697689.1:c.*1307_*1309delinsGCC	ENSP00000513398.1:n.*1307_*1309delinsGCC
ENST00000697690.1:c.771_773delinsGCC	ENSP00000513399.1:p.Arg258Pro
ENST00000697691.1:c.*743_*745delinsGCC	ENSP00000513400.1:n.*743_*745delinsGCC
ENST00000697692.1:c.*783_*785delinsGCC	ENSP00000513401.1:n.*783_*785delinsGCC
ENST00000697694.1:c.420_422delinsGCC	ENSP00000513402.1:p.Arg141Pro
ENST00000697695.1:n.1378_1380delinsGCC
ENST00000337432.9:c.771_773delinsGCC MANE Select	ENSP00000336701.4:p.Arg258Pro
ENST00000337432.8:c.771_773delinsGCC	ENSP00000336701.4:p.Arg258Pro
ENST00000413590.5:c.409_411delinsGCC
ENST00000475762.5:c.*1474_*1476delinsGCC	ENSP00000432421.1:n.*1474_*1476delinsGCC
ENST00000482007.5:c.*199_*201delinsGCC	ENSP00000433332.1:n.*199_*201delinsGCC
ENST00000487525.5:c.*344_*346delinsGCC	ENSP00000431637.1:n.*344_*346delinsGCC
ENST00000578151.1:n.106_108delinsGCC
ENST00000581221.5:n.286_288delinsGCC
ENST00000583539.5:c.771_773delinsGCC	ENSP00000463121.1:p.Arg258Pro
ENST00000584617.5:c.493_495delinsGCC
ENST00000584804.1:c.66_68delinsGCC	ENSP00000463658.1:p.Arg23Pro
NM_058216.2:c.771_773delinsGCC	NP_478123.1:p.Arg258Pro
NR_103872.1:n.675_677delinsGCC
XM_006722001.2:c.771_773delinsGCC	XP_006722064.1:p.Arg258Pro
XM_006722002.2:c.771_773delinsGCC	XP_006722065.1:p.Arg258Pro
XM_006722004.2:c.420_422delinsGCC	XP_006722067.1:p.Arg141Pro
XM_006722005.2:c.420_422delinsGCC	XP_006722068.1:p.Arg141Pro
XM_011525092.1:c.420_422delinsGCC	XP_011523394.1:p.Arg141Pro
XM_011525093.1:c.420_422delinsGCC	XP_011523395.1:p.Arg141Pro
XM_011525094.1:c.420_422delinsGCC	XP_011523396.1:p.Arg141Pro
XR_934513.1:n.989_991delinsGCC
XR_934514.1:n.989_991delinsGCC
XM_006722001.4:c.771_773delinsGCC	XP_006722064.1:p.Arg258Pro
XM_006722002.4:c.771_773delinsGCC	XP_006722065.1:p.Arg258Pro
XM_006722004.3:c.420_422delinsGCC	XP_006722067.1:p.Arg141Pro
XM_006722005.3:c.420_422delinsGCC	XP_006722068.1:p.Arg141Pro
XM_011525092.2:c.420_422delinsGCC	XP_011523394.1:p.Arg141Pro
XM_011525093.2:c.420_422delinsGCC	XP_011523395.1:p.Arg141Pro
XM_011525094.2:c.420_422delinsGCC	XP_011523396.1:p.Arg141Pro
XM_017024914.1:c.420_422delinsGCC	XP_016880403.1:p.Arg141Pro
XM_017024915.1:c.420_422delinsGCC	XP_016880404.1:p.Arg141Pro
XM_017024916.1:c.420_422delinsGCC	XP_016880405.1:p.Arg141Pro
XM_017024917.1:c.420_422delinsGCC	XP_016880406.1:p.Arg141Pro
XM_017024918.2:c.420_422delinsGCC	XP_016880407.1:p.Arg141Pro
XM_017024919.1:c.420_422delinsGCC	XP_016880408.1:p.Arg141Pro
XR_934513.3:n.1420_1422delinsGCC
XR_934514.3:n.1420_1422delinsGCC
NM_058216.3:c.771_773delinsGCC MANE Select	NP_478123.1:p.Arg258Pro
NR_103872.2:n.646_648delinsGCC