Canonical Allele Identifier: CA3057228120

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692653_58692654delinsTC , CM000679.2:g.58692653_58692654delinsTC	GRCh38
NC_000017.10:g.56770014_56770015delinsTC , CM000679.1:g.56770014_56770015delinsTC	GRCh37
NC_000017.9:g.54125013_54125014delinsTC	NCBI36
NG_023199.1:g.5052_5053delinsTC , LRG_314:g.5052_5053delinsTC
NG_047169.1:g.4426_4427delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-239_-238delinsTC	ENSP00000464056.2:n.-239_-238delinsTC
ENST00000697675.1:n.81_82delinsTC
ENST00000697676.1:n.70_71delinsTC
ENST00000697677.1:n.68_69delinsTC
ENST00000697678.1:n.47+21_47+22delinsTC
ENST00000697679.1:n.61_62delinsTC
ENST00000697680.1:c.10_11delinsTC	ENSP00000513392.1:p.Lys4Ser
ENST00000697681.1:c.10_11delinsTC	ENSP00000513393.1:p.Lys4Ser
ENST00000697683.1:c.10_11delinsTC	ENSP00000513395.1:p.Lys4Ser
ENST00000697684.1:n.70_71delinsTC
ENST00000697685.1:c.10_11delinsTC	ENSP00000513396.1:p.Lys4Ser
ENST00000697686.1:c.-207+21_-207+22delinsTC	ENSP00000513397.1:n.-207+21_-207+22delinsTC
ENST00000697687.1:n.56_57delinsTC
ENST00000697688.1:n.56_57delinsTC
ENST00000697689.1:c.10_11delinsTC	ENSP00000513398.1:p.Lys4Ser
ENST00000697690.1:c.10_11delinsTC	ENSP00000513399.1:p.Lys4Ser
ENST00000697691.1:c.10_11delinsTC	ENSP00000513400.1:p.Lys4Ser
ENST00000697692.1:c.10_11delinsTC	ENSP00000513401.1:p.Lys4Ser
ENST00000337432.9:c.10_11delinsTC MANE Select	ENSP00000336701.4:p.Lys4Ser
ENST00000337432.8:c.10_11delinsTC	ENSP00000336701.4:p.Lys4Ser
ENST00000421782.3:c.10_11delinsTC	ENSP00000391450.2:p.Lys4Ser
ENST00000461271.5:c.-239_-238delinsTC	ENSP00000464056.1:n.-239_-238delinsTC
ENST00000475762.5:c.10_11delinsTC	ENSP00000432421.1:p.Lys4Ser
ENST00000476741.2:n.52_53delinsTC
ENST00000482007.5:c.10_11delinsTC	ENSP00000433332.1:p.Lys4Ser
ENST00000486827.1:c.10_11delinsTC	ENSP00000436761.1:p.Lys4Ser
ENST00000487525.5:c.10_11delinsTC	ENSP00000431637.1:p.Lys4Ser
ENST00000487921.5:n.57+21_57+22delinsTC
ENST00000583539.5:c.10_11delinsTC	ENSP00000463121.1:p.Lys4Ser
NM_002876.3:c.10_11delinsTC	NP_002867.1:p.Lys4Ser
NM_058216.2:c.10_11delinsTC	NP_478123.1:p.Lys4Ser
NR_103872.1:n.81_82delinsTC
NR_103873.1:n.81_82delinsTC
XM_006722001.2:c.10_11delinsTC	XP_006722064.1:p.Lys4Ser
XM_006722002.2:c.10_11delinsTC	XP_006722065.1:p.Lys4Ser
XM_006722004.2:c.-239_-238delinsTC	XP_006722067.1:n.-239_-238delinsTC
XM_006722005.2:c.-207+21_-207+22delinsTC	XP_006722068.1:n.-207+21_-207+22delinsTC
XM_011525092.1:c.-539_-538delinsTC	XP_011523394.1:n.-539_-538delinsTC
XM_011525093.1:c.-700_-699delinsTC	XP_011523395.1:n.-700_-699delinsTC
XR_934513.1:n.83_84delinsTC
XR_934514.1:n.83_84delinsTC
XM_006722001.4:c.10_11delinsTC	XP_006722064.1:p.Lys4Ser
XM_006722002.4:c.10_11delinsTC	XP_006722065.1:p.Lys4Ser
XM_006722004.3:c.-239_-238delinsTC	XP_006722067.1:n.-239_-238delinsTC
XM_006722005.3:c.-207+21_-207+22delinsTC	XP_006722068.1:n.-207+21_-207+22delinsTC
XM_017024914.1:c.-239_-238delinsTC	XP_016880403.1:n.-239_-238delinsTC
XM_017024916.1:c.-539_-538delinsTC	XP_016880405.1:n.-539_-538delinsTC
XM_017024917.1:c.-207+21_-207+22delinsTC	XP_016880406.1:n.-207+21_-207+22delinsTC
XM_017024918.2:c.-513_-512delinsTC	XP_016880407.1:n.-513_-512delinsTC
XR_934513.3:n.514_515delinsTC
XR_934514.3:n.514_515delinsTC
NM_058216.3:c.10_11delinsTC MANE Select	NP_478123.1:p.Lys4Ser
NR_103872.2:n.52_53delinsTC
NM_002876.4:c.10_11delinsTC	NP_002867.1:p.Lys4Ser