Canonical Allele Identifier: CA3057228845

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692758_58692759delinsGC , CM000679.2:g.58692758_58692759delinsGC	GRCh38
NC_000017.10:g.56770119_56770120delinsGC , CM000679.1:g.56770119_56770120delinsGC	GRCh37
NC_000017.9:g.54125118_54125119delinsGC	NCBI36
NG_023199.1:g.5157_5158delinsGC , LRG_314:g.5157_5158delinsGC
NG_047169.1:g.4321_4322delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-207+73_-207+74delinsGC	ENSP00000464056.2:n.-207+73_-207+74delinsGC
ENST00000697675.1:n.186_187delinsGC
ENST00000697676.1:n.175_176delinsGC
ENST00000697677.1:n.173_174delinsGC
ENST00000697678.1:n.47+126_47+127delinsGC
ENST00000697679.1:n.166_167delinsGC
ENST00000697680.1:c.115_116delinsGC	ENSP00000513392.1:p.Leu39Ala
ENST00000697681.1:c.115_116delinsGC	ENSP00000513393.1:p.Leu39Ala
ENST00000697683.1:c.115_116delinsGC	ENSP00000513395.1:p.Leu39Ala
ENST00000697684.1:n.175_176delinsGC
ENST00000697685.1:c.115_116delinsGC	ENSP00000513396.1:p.Leu39Ala
ENST00000697686.1:c.-207+126_-207+127delinsGC	ENSP00000513397.1:n.-207+126_-207+127delinsGC
ENST00000697687.1:n.161_162delinsGC
ENST00000697688.1:n.161_162delinsGC
ENST00000697689.1:c.115_116delinsGC	ENSP00000513398.1:p.Leu39Ala
ENST00000697690.1:c.115_116delinsGC	ENSP00000513399.1:p.Leu39Ala
ENST00000697691.1:c.42+73_42+74delinsGC	ENSP00000513400.1:n.42+73_42+74delinsGC
ENST00000697692.1:c.115_116delinsGC	ENSP00000513401.1:p.Leu39Ala
ENST00000697693.1:n.28_29delinsGC
ENST00000337432.9:c.115_116delinsGC MANE Select	ENSP00000336701.4:p.Leu39Ala
ENST00000337432.8:c.115_116delinsGC	ENSP00000336701.4:p.Leu39Ala
ENST00000421782.3:c.115_116delinsGC	ENSP00000391450.2:p.Leu39Ala
ENST00000461271.5:c.-207+73_-207+74delinsGC	ENSP00000464056.1:n.-207+73_-207+74delinsGC
ENST00000475762.5:c.115_116delinsGC	ENSP00000432421.1:p.Leu39Ala
ENST00000476741.2:n.157_158delinsGC
ENST00000482007.5:c.115_116delinsGC	ENSP00000433332.1:p.Leu39Ala
ENST00000486827.1:c.115_116delinsGC	ENSP00000436761.1:p.Leu39Ala
ENST00000487525.5:c.115_116delinsGC	ENSP00000431637.1:p.Leu39Ala
ENST00000487921.5:n.57+126_57+127delinsGC
ENST00000583539.5:c.115_116delinsGC	ENSP00000463121.1:p.Leu39Ala
ENST00000584617.5:c.96_97delinsGC
NM_002876.3:c.115_116delinsGC	NP_002867.1:p.Leu39Ala
NM_058216.2:c.115_116delinsGC	NP_478123.1:p.Leu39Ala
NR_103872.1:n.186_187delinsGC
NR_103873.1:n.113+73_113+74delinsGC
XM_006722001.2:c.115_116delinsGC	XP_006722064.1:p.Leu39Ala
XM_006722002.2:c.115_116delinsGC	XP_006722065.1:p.Leu39Ala
XM_006722004.2:c.-207+73_-207+74delinsGC	XP_006722067.1:n.-207+73_-207+74delinsGC
XM_006722005.2:c.-207+126_-207+127delinsGC	XP_006722068.1:n.-207+126_-207+127delinsGC
XM_011525092.1:c.-507+73_-507+74delinsGC	XP_011523394.1:n.-507+73_-507+74delinsGC
XM_011525093.1:c.-668+73_-668+74delinsGC	XP_011523395.1:n.-668+73_-668+74delinsGC
XR_934513.1:n.188_189delinsGC
XR_934514.1:n.188_189delinsGC
XM_006722001.4:c.115_116delinsGC	XP_006722064.1:p.Leu39Ala
XM_006722002.4:c.115_116delinsGC	XP_006722065.1:p.Leu39Ala
XM_006722004.3:c.-207+73_-207+74delinsGC	XP_006722067.1:n.-207+73_-207+74delinsGC
XM_006722005.3:c.-207+126_-207+127delinsGC	XP_006722068.1:n.-207+126_-207+127delinsGC
XM_011525092.2:c.-507+73_-507+74delinsGC	XP_011523394.1:n.-507+73_-507+74delinsGC
XM_011525093.2:c.-668+73_-668+74delinsGC	XP_011523395.1:n.-668+73_-668+74delinsGC
XM_017024914.1:c.-207+73_-207+74delinsGC	XP_016880403.1:n.-207+73_-207+74delinsGC
XM_017024916.1:c.-507+73_-507+74delinsGC	XP_016880405.1:n.-507+73_-507+74delinsGC
XM_017024917.1:c.-207+126_-207+127delinsGC	XP_016880406.1:n.-207+126_-207+127delinsGC
XM_017024918.2:c.-408_-407delinsGC	XP_016880407.1:n.-408_-407delinsGC
XM_017024919.1:c.-668+73_-668+74delinsGC	XP_016880408.1:n.-668+73_-668+74delinsGC
XR_934513.3:n.619_620delinsGC
XR_934514.3:n.619_620delinsGC
NM_058216.3:c.115_116delinsGC MANE Select	NP_478123.1:p.Leu39Ala
NR_103872.2:n.157_158delinsGC
NM_002876.4:c.115_116delinsGC	NP_002867.1:p.Leu39Ala