Canonical Allele Identifier: CA16620499

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58696830A>G , CM000679.2:g.58696830A>G	GRCh38
NC_000017.10:g.56774191A>G , CM000679.1:g.56774191A>G	GRCh37
NC_000017.9:g.54129190A>G	NCBI36
NG_023199.1:g.9229A>G , LRG_314:g.9229A>G
NG_047169.1:g.250T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_058216.3:c.542A>G MANE Select	NP_478123.1:p.Gln181Arg
ENST00000337432.9:c.542A>G MANE Select	ENSP00000336701.4:p.Gln181Arg
NM_058216.2:c.542A>G	NP_478123.1:p.Gln181Arg
NR_103872.1:n.475+1641A>G
NR_103872.2:n.446+1641A>G
ENST00000337432.8:c.542A>G	ENSP00000336701.4:p.Gln181Arg
ENST00000413590.5:c.180A>G
ENST00000425173.5:c.338A>G	ENSP00000407282.1:p.Gln113Arg
ENST00000461271.5:c.191A>G	ENSP00000464056.1:p.Gln64Arg
ENST00000461271.6:c.191A>G	ENSP00000464056.2:p.Gln64Arg
ENST00000475762.5:c.*1245A>G	ENSP00000432421.1:n.*1245A>G
ENST00000482007.5:c.404+1641A>G	ENSP00000433332.1:n.404+1641A>G
ENST00000487525.5:c.404+1641A>G	ENSP00000431637.1:n.404+1641A>G
ENST00000487921.5:n.454A>G
ENST00000583539.5:c.542A>G	ENSP00000463121.1:p.Gln181Arg
ENST00000584617.5:c.264A>G
ENST00000622327.4:c.278A>G	ENSP00000482326.1:p.Gln93Arg
ENST00000697675.1:n.3139A>G
ENST00000697676.1:n.602A>G
ENST00000697677.1:n.1623A>G
ENST00000697678.1:n.444A>G
ENST00000697679.1:n.1616A>G
ENST00000697680.1:c.*1406A>G	ENSP00000513392.1:n.*1406A>G
ENST00000697681.1:c.*1433A>G	ENSP00000513393.1:n.*1433A>G
ENST00000697683.1:c.*1406A>G	ENSP00000513395.1:n.*1406A>G
ENST00000697684.1:n.602A>G
ENST00000697685.1:c.*1268+1641A>G	ENSP00000513396.1:n.*1268+1641A>G
ENST00000697686.1:c.191A>G	ENSP00000513397.1:p.Gln64Arg
ENST00000697687.1:n.450+1641A>G
ENST00000697688.1:n.588A>G
ENST00000697689.1:c.*1107+1641A>G	ENSP00000513398.1:n.*1107+1641A>G
ENST00000697690.1:c.542A>G	ENSP00000513399.1:p.Gln181Arg
ENST00000697691.1:c.*514A>G	ENSP00000513400.1:n.*514A>G
ENST00000697692.1:c.*554A>G	ENSP00000513401.1:n.*554A>G
ENST00000697694.1:c.191A>G	ENSP00000513402.1:p.Gln64Arg
ENST00000697695.1:n.1149A>G
XM_006722001.2:c.542A>G	XP_006722064.1:p.Gln181Arg
XM_006722001.4:c.542A>G	XP_006722064.1:p.Gln181Arg
XM_006722002.2:c.542A>G	XP_006722065.1:p.Gln181Arg
XM_006722002.4:c.542A>G	XP_006722065.1:p.Gln181Arg
XM_006722004.2:c.191A>G	XP_006722067.1:p.Gln64Arg
XM_006722004.3:c.191A>G	XP_006722067.1:p.Gln64Arg
XM_006722005.2:c.191A>G	XP_006722068.1:p.Gln64Arg
XM_006722005.3:c.191A>G	XP_006722068.1:p.Gln64Arg
XM_011525092.1:c.191A>G	XP_011523394.1:p.Gln64Arg
XM_011525092.2:c.191A>G	XP_011523394.1:p.Gln64Arg
XM_011525093.1:c.191A>G	XP_011523395.1:p.Gln64Arg
XM_011525093.2:c.191A>G	XP_011523395.1:p.Gln64Arg
XM_011525094.1:c.191A>G	XP_011523396.1:p.Gln64Arg
XM_011525094.2:c.191A>G	XP_011523396.1:p.Gln64Arg
XM_017024914.1:c.191A>G	XP_016880403.1:p.Gln64Arg
XM_017024915.1:c.191A>G	XP_016880404.1:p.Gln64Arg
XM_017024916.1:c.191A>G	XP_016880405.1:p.Gln64Arg
XM_017024917.1:c.191A>G	XP_016880406.1:p.Gln64Arg
XM_017024918.2:c.191A>G	XP_016880407.1:p.Gln64Arg
XM_017024919.1:c.191A>G	XP_016880408.1:p.Gln64Arg
XR_934513.1:n.615A>G
XR_934513.3:n.1046A>G
XR_934514.1:n.615A>G
XR_934514.3:n.1046A>G