Canonical Allele Identifier: CA2267814035

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692715_58692716delinsGG , CM000679.2:g.58692715_58692716delinsGG	GRCh38
NC_000017.10:g.56770076_56770077delinsGG , CM000679.1:g.56770076_56770077delinsGG	GRCh37
NC_000017.9:g.54125075_54125076delinsGG	NCBI36
NG_023199.1:g.5114_5115delinsGG , LRG_314:g.5114_5115delinsGG
NG_047169.1:g.4364_4365delinsCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-207+30_-207+31delinsGG	ENSP00000464056.2:n.-207+30_-207+31delinsGG
ENST00000697675.1:n.143_144delinsGG
ENST00000697676.1:n.132_133delinsGG
ENST00000697677.1:n.130_131delinsGG
ENST00000697678.1:n.47+83_47+84delinsGG
ENST00000697679.1:n.123_124delinsGG
ENST00000697680.1:c.72_73delinsGG	ENSP00000513392.1:p.Arg24=
ENST00000697681.1:c.72_73delinsGG	ENSP00000513393.1:p.Arg24=
ENST00000697683.1:c.72_73delinsGG	ENSP00000513395.1:p.Arg24=
ENST00000697684.1:n.132_133delinsGG
ENST00000697685.1:c.72_73delinsGG	ENSP00000513396.1:p.Arg24=
ENST00000697686.1:c.-207+83_-207+84delinsGG	ENSP00000513397.1:n.-207+83_-207+84delinsGG
ENST00000697687.1:n.118_119delinsGG
ENST00000697688.1:n.118_119delinsGG
ENST00000697689.1:c.72_73delinsGG	ENSP00000513398.1:p.Arg24=
ENST00000697690.1:c.72_73delinsGG	ENSP00000513399.1:p.Arg24=
ENST00000697691.1:c.42+30_42+31delinsGG	ENSP00000513400.1:n.42+30_42+31delinsGG
ENST00000697692.1:c.72_73delinsGG	ENSP00000513401.1:p.Arg24=
ENST00000337432.9:c.72_73delinsGG MANE Select	ENSP00000336701.4:p.Arg24=
ENST00000337432.8:c.72_73delinsGG	ENSP00000336701.4:p.Arg24=
ENST00000421782.3:c.72_73delinsGG	ENSP00000391450.2:p.Arg24=
ENST00000461271.5:c.-207+30_-207+31delinsGG	ENSP00000464056.1:n.-207+30_-207+31delinsGG
ENST00000475762.5:c.72_73delinsGG	ENSP00000432421.1:p.Arg24=
ENST00000476741.2:n.114_115delinsGG
ENST00000482007.5:c.72_73delinsGG	ENSP00000433332.1:p.Arg24=
ENST00000486827.1:c.72_73delinsGG	ENSP00000436761.1:p.Arg24=
ENST00000487525.5:c.72_73delinsGG	ENSP00000431637.1:p.Arg24=
ENST00000487921.5:n.57+83_57+84delinsGG
ENST00000583539.5:c.72_73delinsGG	ENSP00000463121.1:p.Arg24=
ENST00000584617.5:c.53_54delinsGG
NM_002876.3:c.72_73delinsGG	NP_002867.1:p.Arg24=
NM_058216.2:c.72_73delinsGG	NP_478123.1:p.Arg24=
NR_103872.1:n.143_144delinsGG
NR_103873.1:n.113+30_113+31delinsGG
XM_006722001.2:c.72_73delinsGG	XP_006722064.1:p.Arg24=
XM_006722002.2:c.72_73delinsGG	XP_006722065.1:p.Arg24=
XM_006722004.2:c.-207+30_-207+31delinsGG	XP_006722067.1:n.-207+30_-207+31delinsGG
XM_006722005.2:c.-207+83_-207+84delinsGG	XP_006722068.1:n.-207+83_-207+84delinsGG
XM_011525092.1:c.-507+30_-507+31delinsGG	XP_011523394.1:n.-507+30_-507+31delinsGG
XM_011525093.1:c.-668+30_-668+31delinsGG	XP_011523395.1:n.-668+30_-668+31delinsGG
XR_934513.1:n.145_146delinsGG
XR_934514.1:n.145_146delinsGG
XM_006722001.4:c.72_73delinsGG	XP_006722064.1:p.Arg24=
XM_006722002.4:c.72_73delinsGG	XP_006722065.1:p.Arg24=
XM_006722004.3:c.-207+30_-207+31delinsGG	XP_006722067.1:n.-207+30_-207+31delinsGG
XM_006722005.3:c.-207+83_-207+84delinsGG	XP_006722068.1:n.-207+83_-207+84delinsGG
XM_011525092.2:c.-507+30_-507+31delinsGG	XP_011523394.1:n.-507+30_-507+31delinsGG
XM_011525093.2:c.-668+30_-668+31delinsGG	XP_011523395.1:n.-668+30_-668+31delinsGG
XM_017024914.1:c.-207+30_-207+31delinsGG	XP_016880403.1:n.-207+30_-207+31delinsGG
XM_017024916.1:c.-507+30_-507+31delinsGG	XP_016880405.1:n.-507+30_-507+31delinsGG
XM_017024917.1:c.-207+83_-207+84delinsGG	XP_016880406.1:n.-207+83_-207+84delinsGG
XM_017024918.2:c.-451_-450delinsGG	XP_016880407.1:n.-451_-450delinsGG
XM_017024919.1:c.-668+30_-668+31delinsGG	XP_016880408.1:n.-668+30_-668+31delinsGG
XR_934513.3:n.576_577delinsGG
XR_934514.3:n.576_577delinsGG
NM_058216.3:c.72_73delinsGG MANE Select	NP_478123.1:p.Arg24=
NR_103872.2:n.114_115delinsGG
NM_002876.4:c.72_73delinsGG	NP_002867.1:p.Arg24=