Canonical Allele Identifier: CA3057227974

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692698_58692700del , CM000679.2:g.58692698_58692700del	GRCh38
NC_000017.10:g.56770059_56770061del , CM000679.1:g.56770059_56770061del	GRCh37
NC_000017.9:g.54125058_54125060del	NCBI36
NG_023199.1:g.5097_5099del , LRG_314:g.5097_5099del
NG_047169.1:g.4381_4383del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-207+13_-207+15del	ENSP00000464056.2:n.-207+13_-207+15del
ENST00000697675.1:n.126_128del
ENST00000697676.1:n.115_117del
ENST00000697677.1:n.113_115del
ENST00000697678.1:n.47+66_47+68del
ENST00000697679.1:n.106_108del
ENST00000697680.1:c.55_57del	ENSP00000513392.1:p.Leu19del
ENST00000697681.1:c.55_57del	ENSP00000513393.1:p.Leu19del
ENST00000697683.1:c.55_57del	ENSP00000513395.1:p.Leu19del
ENST00000697684.1:n.115_117del
ENST00000697685.1:c.55_57del	ENSP00000513396.1:p.Leu19del
ENST00000697686.1:c.-207+66_-207+68del	ENSP00000513397.1:n.-207+66_-207+68del
ENST00000697687.1:n.101_103del
ENST00000697688.1:n.101_103del
ENST00000697689.1:c.55_57del	ENSP00000513398.1:p.Leu19del
ENST00000697690.1:c.55_57del	ENSP00000513399.1:p.Leu19del
ENST00000697691.1:c.42+13_42+15del	ENSP00000513400.1:n.42+13_42+15del
ENST00000697692.1:c.55_57del	ENSP00000513401.1:p.Leu19del
ENST00000337432.9:c.55_57del MANE Select	ENSP00000336701.4:p.Leu19del
ENST00000337432.8:c.55_57del	ENSP00000336701.4:p.Leu19del
ENST00000421782.3:c.55_57del	ENSP00000391450.2:p.Leu19del
ENST00000461271.5:c.-207+13_-207+15del	ENSP00000464056.1:n.-207+13_-207+15del
ENST00000475762.5:c.55_57del	ENSP00000432421.1:p.Leu19del
ENST00000476741.2:n.97_99del
ENST00000482007.5:c.55_57del	ENSP00000433332.1:p.Leu19del
ENST00000486827.1:c.55_57del	ENSP00000436761.1:p.Leu19del
ENST00000487525.5:c.55_57del	ENSP00000431637.1:p.Leu19del
ENST00000487921.5:n.57+66_57+68del
ENST00000583539.5:c.55_57del	ENSP00000463121.1:p.Leu19del
ENST00000584617.5:c.36_38del
NM_002876.3:c.55_57del	NP_002867.1:p.Leu19del
NM_058216.2:c.55_57del	NP_478123.1:p.Leu19del
NR_103872.1:n.126_128del
NR_103873.1:n.113+13_113+15del
XM_006722001.2:c.55_57del	XP_006722064.1:p.Leu19del
XM_006722002.2:c.55_57del	XP_006722065.1:p.Leu19del
XM_006722004.2:c.-207+13_-207+15del	XP_006722067.1:n.-207+13_-207+15del
XM_006722005.2:c.-207+66_-207+68del	XP_006722068.1:n.-207+66_-207+68del
XM_011525092.1:c.-507+13_-507+15del	XP_011523394.1:n.-507+13_-507+15del
XM_011525093.1:c.-668+13_-668+15del	XP_011523395.1:n.-668+13_-668+15del
XR_934513.1:n.128_130del
XR_934514.1:n.128_130del
XM_006722001.4:c.55_57del	XP_006722064.1:p.Leu19del
XM_006722002.4:c.55_57del	XP_006722065.1:p.Leu19del
XM_006722004.3:c.-207+13_-207+15del	XP_006722067.1:n.-207+13_-207+15del
XM_006722005.3:c.-207+66_-207+68del	XP_006722068.1:n.-207+66_-207+68del
XM_011525092.2:c.-507+13_-507+15del	XP_011523394.1:n.-507+13_-507+15del
XM_011525093.2:c.-668+13_-668+15del	XP_011523395.1:n.-668+13_-668+15del
XM_017024914.1:c.-207+13_-207+15del	XP_016880403.1:n.-207+13_-207+15del
XM_017024916.1:c.-507+13_-507+15del	XP_016880405.1:n.-507+13_-507+15del
XM_017024917.1:c.-207+66_-207+68del	XP_016880406.1:n.-207+66_-207+68del
XM_017024918.2:c.-468_-466del	XP_016880407.1:n.-468_-466del
XM_017024919.1:c.-668+13_-668+15del	XP_016880408.1:n.-668+13_-668+15del
XR_934513.3:n.559_561del
XR_934514.3:n.559_561del
NM_058216.3:c.55_57del MANE Select	NP_478123.1:p.Leu19del
NR_103872.2:n.97_99del
NM_002876.4:c.55_57del	NP_002867.1:p.Leu19del