Canonical Allele Identifier: CA3057228119

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692652_58692654delinsAGC , CM000679.2:g.58692652_58692654delinsAGC	GRCh38
NC_000017.10:g.56770013_56770015delinsAGC , CM000679.1:g.56770013_56770015delinsAGC	GRCh37
NC_000017.9:g.54125012_54125014delinsAGC	NCBI36
NG_023199.1:g.5051_5053delinsAGC , LRG_314:g.5051_5053delinsAGC
NG_047169.1:g.4426_4428delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-240_-238delinsAGC	ENSP00000464056.2:n.-240_-238delinsAGC
ENST00000697675.1:n.80_82delinsAGC
ENST00000697676.1:n.69_71delinsAGC
ENST00000697677.1:n.67_69delinsAGC
ENST00000697678.1:n.47+20_47+22delinsAGC
ENST00000697679.1:n.60_62delinsAGC
ENST00000697680.1:c.9_11delinsAGC	ENSP00000513392.1:p.Lys4Ala
ENST00000697681.1:c.9_11delinsAGC	ENSP00000513393.1:p.Lys4Ala
ENST00000697683.1:c.9_11delinsAGC	ENSP00000513395.1:p.Lys4Ala
ENST00000697684.1:n.69_71delinsAGC
ENST00000697685.1:c.9_11delinsAGC	ENSP00000513396.1:p.Lys4Ala
ENST00000697686.1:c.-207+20_-207+22delinsAGC	ENSP00000513397.1:n.-207+20_-207+22delinsAGC
ENST00000697687.1:n.55_57delinsAGC
ENST00000697688.1:n.55_57delinsAGC
ENST00000697689.1:c.9_11delinsAGC	ENSP00000513398.1:p.Lys4Ala
ENST00000697690.1:c.9_11delinsAGC	ENSP00000513399.1:p.Lys4Ala
ENST00000697691.1:c.9_11delinsAGC	ENSP00000513400.1:p.Lys4Ala
ENST00000697692.1:c.9_11delinsAGC	ENSP00000513401.1:p.Lys4Ala
ENST00000337432.9:c.9_11delinsAGC MANE Select	ENSP00000336701.4:p.Lys4Ala
ENST00000337432.8:c.9_11delinsAGC	ENSP00000336701.4:p.Lys4Ala
ENST00000421782.3:c.9_11delinsAGC	ENSP00000391450.2:p.Lys4Ala
ENST00000461271.5:c.-240_-238delinsAGC	ENSP00000464056.1:n.-240_-238delinsAGC
ENST00000475762.5:c.9_11delinsAGC	ENSP00000432421.1:p.Lys4Ala
ENST00000476741.2:n.51_53delinsAGC
ENST00000482007.5:c.9_11delinsAGC	ENSP00000433332.1:p.Lys4Ala
ENST00000486827.1:c.9_11delinsAGC	ENSP00000436761.1:p.Lys4Ala
ENST00000487525.5:c.9_11delinsAGC	ENSP00000431637.1:p.Lys4Ala
ENST00000487921.5:n.57+20_57+22delinsAGC
ENST00000583539.5:c.9_11delinsAGC	ENSP00000463121.1:p.Lys4Ala
NM_002876.3:c.9_11delinsAGC	NP_002867.1:p.Lys4Ala
NM_058216.2:c.9_11delinsAGC	NP_478123.1:p.Lys4Ala
NR_103872.1:n.80_82delinsAGC
NR_103873.1:n.80_82delinsAGC
XM_006722001.2:c.9_11delinsAGC	XP_006722064.1:p.Lys4Ala
XM_006722002.2:c.9_11delinsAGC	XP_006722065.1:p.Lys4Ala
XM_006722004.2:c.-240_-238delinsAGC	XP_006722067.1:n.-240_-238delinsAGC
XM_006722005.2:c.-207+20_-207+22delinsAGC	XP_006722068.1:n.-207+20_-207+22delinsAGC
XM_011525092.1:c.-540_-538delinsAGC	XP_011523394.1:n.-540_-538delinsAGC
XM_011525093.1:c.-701_-699delinsAGC	XP_011523395.1:n.-701_-699delinsAGC
XR_934513.1:n.82_84delinsAGC
XR_934514.1:n.82_84delinsAGC
XM_006722001.4:c.9_11delinsAGC	XP_006722064.1:p.Lys4Ala
XM_006722002.4:c.9_11delinsAGC	XP_006722065.1:p.Lys4Ala
XM_006722004.3:c.-240_-238delinsAGC	XP_006722067.1:n.-240_-238delinsAGC
XM_006722005.3:c.-207+20_-207+22delinsAGC	XP_006722068.1:n.-207+20_-207+22delinsAGC
XM_017024914.1:c.-240_-238delinsAGC	XP_016880403.1:n.-240_-238delinsAGC
XM_017024916.1:c.-540_-538delinsAGC	XP_016880405.1:n.-540_-538delinsAGC
XM_017024917.1:c.-207+20_-207+22delinsAGC	XP_016880406.1:n.-207+20_-207+22delinsAGC
XM_017024918.2:c.-514_-512delinsAGC	XP_016880407.1:n.-514_-512delinsAGC
XR_934513.3:n.513_515delinsAGC
XR_934514.3:n.513_515delinsAGC
NM_058216.3:c.9_11delinsAGC MANE Select	NP_478123.1:p.Lys4Ala
NR_103872.2:n.51_53delinsAGC
NM_002876.4:c.9_11delinsAGC	NP_002867.1:p.Lys4Ala