Canonical Allele Identifier: CA2733775142

Gene: RAD51C

Linked Data

• dbSNP Id: rs2143677258

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692725del , CM000679.2:g.58692725del	GRCh38
NC_000017.10:g.56770086del , CM000679.1:g.56770086del	GRCh37
NC_000017.9:g.54125085del	NCBI36
NG_023199.1:g.5124del , LRG_314:g.5124del
NG_047169.1:g.4356del

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.-207+40del	ENSP00000464056.2:n.-207+40del
ENST00000697675.1:n.153del
ENST00000697676.1:n.142del
ENST00000697677.1:n.140del
ENST00000697678.1:n.47+93del
ENST00000697679.1:n.133del
ENST00000697680.1:c.82del	ENSP00000513392.1:p.Val28CysfsTer12
ENST00000697681.1:c.82del	ENSP00000513393.1:p.Val28CysfsTer12
ENST00000697683.1:c.82del	ENSP00000513395.1:p.Val28CysfsTer12
ENST00000697684.1:n.142del
ENST00000697685.1:c.82del	ENSP00000513396.1:p.Val28CysfsTer12
ENST00000697686.1:c.-207+93del	ENSP00000513397.1:n.-207+93del
ENST00000697687.1:n.128del
ENST00000697688.1:n.128del
ENST00000697689.1:c.82del	ENSP00000513398.1:p.Val28CysfsTer12
ENST00000697690.1:c.82del	ENSP00000513399.1:p.Val28CysfsTer12
ENST00000697691.1:c.42+40del	ENSP00000513400.1:n.42+40del
ENST00000697692.1:c.82del	ENSP00000513401.1:p.Val28CysfsTer12
ENST00000337432.9:c.82del MANE Select	ENSP00000336701.4:p.Val28CysfsTer12
ENST00000337432.8:c.82del	ENSP00000336701.4:p.Val28CysfsTer12
ENST00000421782.3:c.82del	ENSP00000391450.2:p.Val28CysfsTer12
ENST00000461271.5:c.-207+40del	ENSP00000464056.1:n.-207+40del
ENST00000475762.5:c.82del	ENSP00000432421.1:p.Val28CysfsTer12
ENST00000476741.2:n.124del
ENST00000482007.5:c.82del	ENSP00000433332.1:p.Val28CysfsTer12
ENST00000486827.1:c.82del	ENSP00000436761.1:p.Val28CysfsTer12
ENST00000487525.5:c.82del	ENSP00000431637.1:p.Val28CysfsTer12
ENST00000487921.5:n.57+93del
ENST00000583539.5:c.82del	ENSP00000463121.1:p.Val28CysfsTer12
ENST00000584617.5:c.63del
NM_002876.3:c.82del	NP_002867.1:p.Val28CysfsTer12
NM_058216.2:c.82del	NP_478123.1:p.Val28CysfsTer12
NR_103872.1:n.153del
NR_103873.1:n.113+40del
XM_006722001.2:c.82del	XP_006722064.1:p.Val28CysfsTer12
XM_006722002.2:c.82del	XP_006722065.1:p.Val28CysfsTer12
XM_006722004.2:c.-207+40del	XP_006722067.1:n.-207+40del
XM_006722005.2:c.-207+93del	XP_006722068.1:n.-207+93del
XM_011525092.1:c.-507+40del	XP_011523394.1:n.-507+40del
XM_011525093.1:c.-668+40del	XP_011523395.1:n.-668+40del
XR_934513.1:n.155del
XR_934514.1:n.155del
XM_006722001.4:c.82del	XP_006722064.1:p.Val28CysfsTer12
XM_006722002.4:c.82del	XP_006722065.1:p.Val28CysfsTer12
XM_006722004.3:c.-207+40del	XP_006722067.1:n.-207+40del
XM_006722005.3:c.-207+93del	XP_006722068.1:n.-207+93del
XM_011525092.2:c.-507+40del	XP_011523394.1:n.-507+40del
XM_011525093.2:c.-668+40del	XP_011523395.1:n.-668+40del
XM_017024914.1:c.-207+40del	XP_016880403.1:n.-207+40del
XM_017024916.1:c.-507+40del	XP_016880405.1:n.-507+40del
XM_017024917.1:c.-207+93del	XP_016880406.1:n.-207+93del
XM_017024918.2:c.-441del	XP_016880407.1:n.-441del
XM_017024919.1:c.-668+40del	XP_016880408.1:n.-668+40del
XR_934513.3:n.586del
XR_934514.3:n.586del
NM_058216.3:c.82del MANE Select	NP_478123.1:p.Val28CysfsTer12
NR_103872.2:n.124del
NM_002876.4:c.82del	NP_002867.1:p.Val28CysfsTer12