Canonical Allele Identifier: CA773574964

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58699722A>G , CM000679.2:g.58699722A>G	GRCh38
NC_000017.10:g.56777083A>G , CM000679.1:g.56777083A>G	GRCh37
NC_000017.9:g.54132082A>G	NCBI36
NG_023199.1:g.12121A>G , LRG_314:g.12121A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_058216.3:c.571+2863A>G MANE Select	NP_478123.1:n.571+2863A>G
ENST00000337432.9:c.571+2863A>G MANE Select	ENSP00000336701.4:n.571+2863A>G
NM_058216.2:c.571+2863A>G	NP_478123.1:n.571+2863A>G
NR_103872.1:n.476-3474A>G
NR_103872.2:n.447-3474A>G
ENST00000337432.8:c.571+2863A>G	ENSP00000336701.4:n.571+2863A>G
ENST00000413590.5:c.209+2863A>G
ENST00000425173.5:c.367+2863A>G	ENSP00000407282.1:n.367+2863A>G
ENST00000461271.5:c.220+2863A>G	ENSP00000464056.1:n.220+2863A>G
ENST00000461271.6:c.220+2863A>G	ENSP00000464056.2:n.220+2863A>G
ENST00000475762.5:c.*1274+2863A>G	ENSP00000432421.1:n.*1274+2863A>G
ENST00000482007.5:c.405-3474A>G	ENSP00000433332.1:n.405-3474A>G
ENST00000487525.5:c.405-3474A>G	ENSP00000431637.1:n.405-3474A>G
ENST00000487921.5:n.483+2863A>G
ENST00000583539.5:c.571+2863A>G	ENSP00000463121.1:n.571+2863A>G
ENST00000584617.5:c.293+2863A>G
ENST00000622327.4:c.308-153A>G	ENSP00000482326.1:n.308-153A>G
ENST00000697676.1:n.632-1874A>G
ENST00000697677.1:n.1652+2863A>G
ENST00000697678.1:n.473+2863A>G
ENST00000697679.1:n.1645+2863A>G
ENST00000697680.1:c.*1435+2863A>G	ENSP00000513392.1:n.*1435+2863A>G
ENST00000697681.1:c.*1463-153A>G	ENSP00000513393.1:n.*1463-153A>G
ENST00000697683.1:c.*1435+2863A>G	ENSP00000513395.1:n.*1435+2863A>G
ENST00000697684.1:n.631+2863A>G
ENST00000697685.1:c.*1269-3474A>G	ENSP00000513396.1:n.*1269-3474A>G
ENST00000697686.1:c.220+2863A>G	ENSP00000513397.1:n.220+2863A>G
ENST00000697687.1:n.451-3474A>G
ENST00000697688.1:n.617+2863A>G
ENST00000697689.1:c.*1108-3474A>G	ENSP00000513398.1:n.*1108-3474A>G
ENST00000697690.1:c.571+2863A>G	ENSP00000513399.1:n.571+2863A>G
ENST00000697691.1:c.*543+2863A>G	ENSP00000513400.1:n.*543+2863A>G
ENST00000697692.1:c.*583+2863A>G	ENSP00000513401.1:n.*583+2863A>G
ENST00000697694.1:c.220+2863A>G	ENSP00000513402.1:n.220+2863A>G
ENST00000697695.1:n.1178+2863A>G
XM_006722001.2:c.571+2863A>G	XP_006722064.1:n.571+2863A>G
XM_006722001.4:c.571+2863A>G	XP_006722064.1:n.571+2863A>G
XM_006722002.2:c.571+2863A>G	XP_006722065.1:n.571+2863A>G
XM_006722002.4:c.571+2863A>G	XP_006722065.1:n.571+2863A>G
XM_006722004.2:c.220+2863A>G	XP_006722067.1:n.220+2863A>G
XM_006722004.3:c.220+2863A>G	XP_006722067.1:n.220+2863A>G
XM_006722005.2:c.220+2863A>G	XP_006722068.1:n.220+2863A>G
XM_006722005.3:c.220+2863A>G	XP_006722068.1:n.220+2863A>G
XM_011525092.1:c.220+2863A>G	XP_011523394.1:n.220+2863A>G
XM_011525092.2:c.220+2863A>G	XP_011523394.1:n.220+2863A>G
XM_011525093.1:c.220+2863A>G	XP_011523395.1:n.220+2863A>G
XM_011525093.2:c.220+2863A>G	XP_011523395.1:n.220+2863A>G
XM_011525094.1:c.220+2863A>G	XP_011523396.1:n.220+2863A>G
XM_011525094.2:c.220+2863A>G	XP_011523396.1:n.220+2863A>G
XM_017024914.1:c.220+2863A>G	XP_016880403.1:n.220+2863A>G
XM_017024915.1:c.220+2863A>G	XP_016880404.1:n.220+2863A>G
XM_017024916.1:c.220+2863A>G	XP_016880405.1:n.220+2863A>G
XM_017024917.1:c.220+2863A>G	XP_016880406.1:n.220+2863A>G
XM_017024918.2:c.220+2863A>G	XP_016880407.1:n.220+2863A>G
XM_017024919.1:c.220+2863A>G	XP_016880408.1:n.220+2863A>G
XR_934513.1:n.644+2863A>G
XR_934513.3:n.1075+2863A>G
XR_934514.1:n.644+2863A>G
XR_934514.3:n.1075+2863A>G