Canonical Allele Identifier: CA3060598349

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692657_58692658delinsGC , CM000679.2:g.58692657_58692658delinsGC	GRCh38
NC_000017.10:g.56770018_56770019delinsGC , CM000679.1:g.56770018_56770019delinsGC	GRCh37
NC_000017.9:g.54125017_54125018delinsGC	NCBI36
NG_023199.1:g.5056_5057delinsGC , LRG_314:g.5056_5057delinsGC
NG_047169.1:g.4422_4423delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-235_-234delinsGC	ENSP00000464056.2:n.-235_-234delinsGC
ENST00000697675.1:n.85_86delinsGC
ENST00000697676.1:n.74_75delinsGC
ENST00000697677.1:n.72_73delinsGC
ENST00000697678.1:n.47+25_47+26delinsGC
ENST00000697679.1:n.65_66delinsGC
ENST00000697680.1:c.14_15delinsGC	ENSP00000513392.1:p.Thr5Ser
ENST00000697681.1:c.14_15delinsGC	ENSP00000513393.1:p.Thr5Ser
ENST00000697683.1:c.14_15delinsGC	ENSP00000513395.1:p.Thr5Ser
ENST00000697684.1:n.74_75delinsGC
ENST00000697685.1:c.14_15delinsGC	ENSP00000513396.1:p.Thr5Ser
ENST00000697686.1:c.-207+25_-207+26delinsGC	ENSP00000513397.1:n.-207+25_-207+26delinsGC
ENST00000697687.1:n.60_61delinsGC
ENST00000697688.1:n.60_61delinsGC
ENST00000697689.1:c.14_15delinsGC	ENSP00000513398.1:p.Thr5Ser
ENST00000697690.1:c.14_15delinsGC	ENSP00000513399.1:p.Thr5Ser
ENST00000697691.1:c.14_15delinsGC	ENSP00000513400.1:p.Thr5Ser
ENST00000697692.1:c.14_15delinsGC	ENSP00000513401.1:p.Thr5Ser
ENST00000337432.9:c.14_15delinsGC MANE Select	ENSP00000336701.4:p.Thr5Ser
ENST00000337432.8:c.14_15delinsGC	ENSP00000336701.4:p.Thr5Ser
ENST00000421782.3:c.14_15delinsGC	ENSP00000391450.2:p.Thr5Ser
ENST00000461271.5:c.-235_-234delinsGC	ENSP00000464056.1:n.-235_-234delinsGC
ENST00000475762.5:c.14_15delinsGC	ENSP00000432421.1:p.Thr5Ser
ENST00000476741.2:n.56_57delinsGC
ENST00000482007.5:c.14_15delinsGC	ENSP00000433332.1:p.Thr5Ser
ENST00000486827.1:c.14_15delinsGC	ENSP00000436761.1:p.Thr5Ser
ENST00000487525.5:c.14_15delinsGC	ENSP00000431637.1:p.Thr5Ser
ENST00000487921.5:n.57+25_57+26delinsGC
ENST00000583539.5:c.14_15delinsGC	ENSP00000463121.1:p.Thr5Ser
NM_002876.3:c.14_15delinsGC	NP_002867.1:p.Thr5Ser
NM_058216.2:c.14_15delinsGC	NP_478123.1:p.Thr5Ser
NR_103872.1:n.85_86delinsGC
NR_103873.1:n.85_86delinsGC
XM_006722001.2:c.14_15delinsGC	XP_006722064.1:p.Thr5Ser
XM_006722002.2:c.14_15delinsGC	XP_006722065.1:p.Thr5Ser
XM_006722004.2:c.-235_-234delinsGC	XP_006722067.1:n.-235_-234delinsGC
XM_006722005.2:c.-207+25_-207+26delinsGC	XP_006722068.1:n.-207+25_-207+26delinsGC
XM_011525092.1:c.-535_-534delinsGC	XP_011523394.1:n.-535_-534delinsGC
XM_011525093.1:c.-696_-695delinsGC	XP_011523395.1:n.-696_-695delinsGC
XR_934513.1:n.87_88delinsGC
XR_934514.1:n.87_88delinsGC
XM_006722001.4:c.14_15delinsGC	XP_006722064.1:p.Thr5Ser
XM_006722002.4:c.14_15delinsGC	XP_006722065.1:p.Thr5Ser
XM_006722004.3:c.-235_-234delinsGC	XP_006722067.1:n.-235_-234delinsGC
XM_006722005.3:c.-207+25_-207+26delinsGC	XP_006722068.1:n.-207+25_-207+26delinsGC
XM_017024914.1:c.-235_-234delinsGC	XP_016880403.1:n.-235_-234delinsGC
XM_017024916.1:c.-535_-534delinsGC	XP_016880405.1:n.-535_-534delinsGC
XM_017024917.1:c.-207+25_-207+26delinsGC	XP_016880406.1:n.-207+25_-207+26delinsGC
XM_017024918.2:c.-509_-508delinsGC	XP_016880407.1:n.-509_-508delinsGC
XR_934513.3:n.518_519delinsGC
XR_934514.3:n.518_519delinsGC
NM_058216.3:c.14_15delinsGC MANE Select	NP_478123.1:p.Thr5Ser
NR_103872.2:n.56_57delinsGC
NM_002876.4:c.14_15delinsGC	NP_002867.1:p.Thr5Ser