Canonical Allele Identifier: CA3057228112

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692647_58692648delinsAC , CM000679.2:g.58692647_58692648delinsAC	GRCh38
NC_000017.10:g.56770008_56770009delinsAC , CM000679.1:g.56770008_56770009delinsAC	GRCh37
NC_000017.9:g.54125007_54125008delinsAC	NCBI36
NG_023199.1:g.5046_5047delinsAC , LRG_314:g.5046_5047delinsAC
NG_047169.1:g.4432_4433delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-245_-244delinsAC	ENSP00000464056.2:n.-245_-244delinsAC
ENST00000697675.1:n.75_76delinsAC
ENST00000697676.1:n.64_65delinsAC
ENST00000697677.1:n.62_63delinsAC
ENST00000697678.1:n.47+15_47+16delinsAC
ENST00000697679.1:n.55_56delinsAC
ENST00000697680.1:c.4_5delinsAC	ENSP00000513392.1:p.Arg2Thr
ENST00000697681.1:c.4_5delinsAC	ENSP00000513393.1:p.Arg2Thr
ENST00000697683.1:c.4_5delinsAC	ENSP00000513395.1:p.Arg2Thr
ENST00000697684.1:n.64_65delinsAC
ENST00000697685.1:c.4_5delinsAC	ENSP00000513396.1:p.Arg2Thr
ENST00000697686.1:c.-207+15_-207+16delinsAC	ENSP00000513397.1:n.-207+15_-207+16delinsAC
ENST00000697687.1:n.50_51delinsAC
ENST00000697688.1:n.50_51delinsAC
ENST00000697689.1:c.4_5delinsAC	ENSP00000513398.1:p.Arg2Thr
ENST00000697690.1:c.4_5delinsAC	ENSP00000513399.1:p.Arg2Thr
ENST00000697691.1:c.4_5delinsAC	ENSP00000513400.1:p.Arg2Thr
ENST00000697692.1:c.4_5delinsAC	ENSP00000513401.1:p.Arg2Thr
ENST00000337432.9:c.4_5delinsAC MANE Select	ENSP00000336701.4:p.Arg2Thr
ENST00000337432.8:c.4_5delinsAC	ENSP00000336701.4:p.Arg2Thr
ENST00000421782.3:c.4_5delinsAC	ENSP00000391450.2:p.Arg2Thr
ENST00000461271.5:c.-245_-244delinsAC	ENSP00000464056.1:n.-245_-244delinsAC
ENST00000475762.5:c.4_5delinsAC	ENSP00000432421.1:p.Arg2Thr
ENST00000476741.2:n.46_47delinsAC
ENST00000482007.5:c.4_5delinsAC	ENSP00000433332.1:p.Arg2Thr
ENST00000486827.1:c.4_5delinsAC	ENSP00000436761.1:p.Arg2Thr
ENST00000487525.5:c.4_5delinsAC	ENSP00000431637.1:p.Arg2Thr
ENST00000487921.5:n.57+15_57+16delinsAC
ENST00000583539.5:c.4_5delinsAC	ENSP00000463121.1:p.Arg2Thr
NM_002876.3:c.4_5delinsAC	NP_002867.1:p.Arg2Thr
NM_058216.2:c.4_5delinsAC	NP_478123.1:p.Arg2Thr
NR_103872.1:n.75_76delinsAC
NR_103873.1:n.75_76delinsAC
XM_006722001.2:c.4_5delinsAC	XP_006722064.1:p.Arg2Thr
XM_006722002.2:c.4_5delinsAC	XP_006722065.1:p.Arg2Thr
XM_006722004.2:c.-245_-244delinsAC	XP_006722067.1:n.-245_-244delinsAC
XM_006722005.2:c.-207+15_-207+16delinsAC	XP_006722068.1:n.-207+15_-207+16delinsAC
XM_011525092.1:c.-545_-544delinsAC	XP_011523394.1:n.-545_-544delinsAC
XM_011525093.1:c.-706_-705delinsAC	XP_011523395.1:n.-706_-705delinsAC
XR_934513.1:n.77_78delinsAC
XR_934514.1:n.77_78delinsAC
XM_006722001.4:c.4_5delinsAC	XP_006722064.1:p.Arg2Thr
XM_006722002.4:c.4_5delinsAC	XP_006722065.1:p.Arg2Thr
XM_006722004.3:c.-245_-244delinsAC	XP_006722067.1:n.-245_-244delinsAC
XM_006722005.3:c.-207+15_-207+16delinsAC	XP_006722068.1:n.-207+15_-207+16delinsAC
XM_017024914.1:c.-245_-244delinsAC	XP_016880403.1:n.-245_-244delinsAC
XM_017024916.1:c.-545_-544delinsAC	XP_016880405.1:n.-545_-544delinsAC
XM_017024917.1:c.-207+15_-207+16delinsAC	XP_016880406.1:n.-207+15_-207+16delinsAC
XM_017024918.2:c.-519_-518delinsAC	XP_016880407.1:n.-519_-518delinsAC
XR_934513.3:n.508_509delinsAC
XR_934514.3:n.508_509delinsAC
NM_058216.3:c.4_5delinsAC MANE Select	NP_478123.1:p.Arg2Thr
NR_103872.2:n.46_47delinsAC
NM_002876.4:c.4_5delinsAC	NP_002867.1:p.Arg2Thr