Canonical Allele Identifier: CA2267822517

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58709926_58709927delinsGT , CM000679.2:g.58709926_58709927delinsGT	GRCh38
NC_000017.10:g.56787287_56787288delinsGT , CM000679.1:g.56787287_56787288delinsGT	GRCh37
NC_000017.9:g.54142286_54142287delinsGT	NCBI36
NG_023199.1:g.22325_22326delinsGT , LRG_314:g.22325_22326delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.422_423delinsGT	ENSP00000464056.2:p.Arg141=
ENST00000697678.1:n.675_676delinsGT
ENST00000697679.1:n.1847_1848delinsGT
ENST00000697680.1:c.*1637_*1638delinsGT	ENSP00000513392.1:n.*1637_*1638delinsGT
ENST00000697681.1:c.*1934_*1935delinsGT	ENSP00000513393.1:n.*1934_*1935delinsGT
ENST00000697683.1:c.*1637_*1638delinsGT	ENSP00000513395.1:n.*1637_*1638delinsGT
ENST00000697684.1:n.833_834delinsGT
ENST00000697685.1:c.*1470_*1471delinsGT	ENSP00000513396.1:n.*1470_*1471delinsGT
ENST00000697686.1:c.422_423delinsGT	ENSP00000513397.1:p.Arg141=
ENST00000697687.1:n.652_653delinsGT
ENST00000697688.1:n.819_820delinsGT
ENST00000697689.1:c.*1309_*1310delinsGT	ENSP00000513398.1:n.*1309_*1310delinsGT
ENST00000697690.1:c.773_774delinsGT	ENSP00000513399.1:p.Arg258=
ENST00000697691.1:c.*745_*746delinsGT	ENSP00000513400.1:n.*745_*746delinsGT
ENST00000697692.1:c.*785_*786delinsGT	ENSP00000513401.1:n.*785_*786delinsGT
ENST00000697694.1:c.422_423delinsGT	ENSP00000513402.1:p.Arg141=
ENST00000697695.1:n.1380_1381delinsGT
ENST00000337432.9:c.773_774delinsGT MANE Select	ENSP00000336701.4:p.Arg258=
ENST00000337432.8:c.773_774delinsGT	ENSP00000336701.4:p.Arg258=
ENST00000413590.5:c.411_412delinsGT
ENST00000475762.5:c.*1476_*1477delinsGT	ENSP00000432421.1:n.*1476_*1477delinsGT
ENST00000482007.5:c.*201_*202delinsGT	ENSP00000433332.1:n.*201_*202delinsGT
ENST00000487525.5:c.*346_*347delinsGT	ENSP00000431637.1:n.*346_*347delinsGT
ENST00000578151.1:n.108_109delinsGT
ENST00000581221.5:n.288_289delinsGT
ENST00000583539.5:c.773_774delinsGT	ENSP00000463121.1:p.Arg258=
ENST00000584617.5:c.495_496delinsGT
ENST00000584804.1:c.68_69delinsGT	ENSP00000463658.1:p.Arg23=
NM_058216.2:c.773_774delinsGT	NP_478123.1:p.Arg258=
NR_103872.1:n.677_678delinsGT
XM_006722001.2:c.773_774delinsGT	XP_006722064.1:p.Arg258=
XM_006722002.2:c.773_774delinsGT	XP_006722065.1:p.Arg258=
XM_006722004.2:c.422_423delinsGT	XP_006722067.1:p.Arg141=
XM_006722005.2:c.422_423delinsGT	XP_006722068.1:p.Arg141=
XM_011525092.1:c.422_423delinsGT	XP_011523394.1:p.Arg141=
XM_011525093.1:c.422_423delinsGT	XP_011523395.1:p.Arg141=
XM_011525094.1:c.422_423delinsGT	XP_011523396.1:p.Arg141=
XR_934513.1:n.991_992delinsGT
XR_934514.1:n.991_992delinsGT
XM_006722001.4:c.773_774delinsGT	XP_006722064.1:p.Arg258=
XM_006722002.4:c.773_774delinsGT	XP_006722065.1:p.Arg258=
XM_006722004.3:c.422_423delinsGT	XP_006722067.1:p.Arg141=
XM_006722005.3:c.422_423delinsGT	XP_006722068.1:p.Arg141=
XM_011525092.2:c.422_423delinsGT	XP_011523394.1:p.Arg141=
XM_011525093.2:c.422_423delinsGT	XP_011523395.1:p.Arg141=
XM_011525094.2:c.422_423delinsGT	XP_011523396.1:p.Arg141=
XM_017024914.1:c.422_423delinsGT	XP_016880403.1:p.Arg141=
XM_017024915.1:c.422_423delinsGT	XP_016880404.1:p.Arg141=
XM_017024916.1:c.422_423delinsGT	XP_016880405.1:p.Arg141=
XM_017024917.1:c.422_423delinsGT	XP_016880406.1:p.Arg141=
XM_017024918.2:c.422_423delinsGT	XP_016880407.1:p.Arg141=
XM_017024919.1:c.422_423delinsGT	XP_016880408.1:p.Arg141=
XR_934513.3:n.1422_1423delinsGT
XR_934514.3:n.1422_1423delinsGT
NM_058216.3:c.773_774delinsGT MANE Select	NP_478123.1:p.Arg258=
NR_103872.2:n.648_649delinsGT