Canonical Allele Identifier: CA3057242353

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703254_58703256delinsGCC , CM000679.2:g.58703254_58703256delinsGCC	GRCh38
NC_000017.10:g.56780615_56780617delinsGCC , CM000679.1:g.56780615_56780617delinsGCC	GRCh37
NC_000017.9:g.54135614_54135616delinsGCC	NCBI36
NG_023199.1:g.15653_15655delinsGCC , LRG_314:g.15653_15655delinsGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.279_281delinsGCC	ENSP00000464056.2:p.Tyr93Ter
ENST00000697677.1:n.1711_1713delinsGCC
ENST00000697678.1:n.532_534delinsGCC
ENST00000697679.1:n.1704_1706delinsGCC
ENST00000697680.1:c.*1494_*1496delinsGCC	ENSP00000513392.1:n.*1494_*1496delinsGCC
ENST00000697681.1:c.*1646_*1648delinsGCC	ENSP00000513393.1:n.*1646_*1648delinsGCC
ENST00000697683.1:c.*1494_*1496delinsGCC	ENSP00000513395.1:n.*1494_*1496delinsGCC
ENST00000697684.1:n.690_692delinsGCC
ENST00000697685.1:c.*1327_*1329delinsGCC	ENSP00000513396.1:n.*1327_*1329delinsGCC
ENST00000697686.1:c.279_281delinsGCC	ENSP00000513397.1:p.Tyr93Ter
ENST00000697687.1:n.509_511delinsGCC
ENST00000697688.1:n.676_678delinsGCC
ENST00000697689.1:c.*1166_*1168delinsGCC	ENSP00000513398.1:n.*1166_*1168delinsGCC
ENST00000697690.1:c.630_632delinsGCC	ENSP00000513399.1:p.Tyr210Ter
ENST00000697691.1:c.*602_*604delinsGCC	ENSP00000513400.1:n.*602_*604delinsGCC
ENST00000697692.1:c.*642_*644delinsGCC	ENSP00000513401.1:n.*642_*644delinsGCC
ENST00000697694.1:c.279_281delinsGCC	ENSP00000513402.1:p.Tyr93Ter
ENST00000697695.1:n.1237_1239delinsGCC
ENST00000337432.9:c.630_632delinsGCC MANE Select	ENSP00000336701.4:p.Tyr210Ter
ENST00000337432.8:c.630_632delinsGCC	ENSP00000336701.4:p.Tyr210Ter
ENST00000413590.5:c.268_270delinsGCC
ENST00000425173.5:c.426_428delinsGCC	ENSP00000407282.1:p.Tyr142Ter
ENST00000461271.5:c.279_281delinsGCC	ENSP00000464056.1:p.Tyr93Ter
ENST00000475762.5:c.*1333_*1335delinsGCC	ENSP00000432421.1:n.*1333_*1335delinsGCC
ENST00000482007.5:c.*58_*60delinsGCC	ENSP00000433332.1:n.*58_*60delinsGCC
ENST00000487525.5:c.*58_*60delinsGCC	ENSP00000431637.1:n.*58_*60delinsGCC
ENST00000487921.5:n.542_544delinsGCC
ENST00000583539.5:c.630_632delinsGCC	ENSP00000463121.1:p.Tyr210Ter
ENST00000584617.5:c.352_354delinsGCC
NM_058216.2:c.630_632delinsGCC	NP_478123.1:p.Tyr210Ter
NR_103872.1:n.534_536delinsGCC
XM_006722001.2:c.630_632delinsGCC	XP_006722064.1:p.Tyr210Ter
XM_006722002.2:c.630_632delinsGCC	XP_006722065.1:p.Tyr210Ter
XM_006722004.2:c.279_281delinsGCC	XP_006722067.1:p.Tyr93Ter
XM_006722005.2:c.279_281delinsGCC	XP_006722068.1:p.Tyr93Ter
XM_011525092.1:c.279_281delinsGCC	XP_011523394.1:p.Tyr93Ter
XM_011525093.1:c.279_281delinsGCC	XP_011523395.1:p.Tyr93Ter
XM_011525094.1:c.279_281delinsGCC	XP_011523396.1:p.Tyr93Ter
XR_934513.1:n.703_705delinsGCC
XR_934514.1:n.703_705delinsGCC
XM_006722001.4:c.630_632delinsGCC	XP_006722064.1:p.Tyr210Ter
XM_006722002.4:c.630_632delinsGCC	XP_006722065.1:p.Tyr210Ter
XM_006722004.3:c.279_281delinsGCC	XP_006722067.1:p.Tyr93Ter
XM_006722005.3:c.279_281delinsGCC	XP_006722068.1:p.Tyr93Ter
XM_011525092.2:c.279_281delinsGCC	XP_011523394.1:p.Tyr93Ter
XM_011525093.2:c.279_281delinsGCC	XP_011523395.1:p.Tyr93Ter
XM_011525094.2:c.279_281delinsGCC	XP_011523396.1:p.Tyr93Ter
XM_017024914.1:c.279_281delinsGCC	XP_016880403.1:p.Tyr93Ter
XM_017024915.1:c.279_281delinsGCC	XP_016880404.1:p.Tyr93Ter
XM_017024916.1:c.279_281delinsGCC	XP_016880405.1:p.Tyr93Ter
XM_017024917.1:c.279_281delinsGCC	XP_016880406.1:p.Tyr93Ter
XM_017024918.2:c.279_281delinsGCC	XP_016880407.1:p.Tyr93Ter
XM_017024919.1:c.279_281delinsGCC	XP_016880408.1:p.Tyr93Ter
XR_934513.3:n.1134_1136delinsGCC
XR_934514.3:n.1134_1136delinsGCC
NM_058216.3:c.630_632delinsGCC MANE Select	NP_478123.1:p.Tyr210Ter
NR_103872.2:n.505_507delinsGCC