Canonical Allele Identifier: CA400366639

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58734211G>A , CM000679.2:g.58734211G>A	GRCh38
NC_000017.10:g.56811572G>A , CM000679.1:g.56811572G>A	GRCh37
NC_000017.9:g.54166571G>A	NCBI36
NG_023199.1:g.46610G>A , LRG_314:g.46610G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_058216.3:c.1120G>A MANE Select	NP_478123.1:p.Glu374Lys
ENST00000337432.9:c.1120G>A MANE Select	ENSP00000336701.4:p.Glu374Lys
NM_058216.2:c.1120G>A	NP_478123.1:p.Glu374Lys
NR_103872.1:n.1024G>A
NR_103872.2:n.995G>A
ENST00000337432.8:c.1120G>A	ENSP00000336701.4:p.Glu374Lys
ENST00000413590.5:c.761G>A
ENST00000461271.6:c.*1652G>A	ENSP00000464056.2:n.*1652G>A
ENST00000461706.1:n.307G>A
ENST00000475762.5:c.*1756G>A	ENSP00000432421.1:n.*1756G>A
ENST00000482007.5:c.*548G>A	ENSP00000433332.1:n.*548G>A
ENST00000487525.5:c.*696G>A	ENSP00000431637.1:n.*696G>A
ENST00000578151.1:n.333G>A
ENST00000581221.5:n.635G>A
ENST00000584804.1:c.354G>A	ENSP00000463658.1:n.354G>A
ENST00000697680.1:c.*2084G>A	ENSP00000513392.1:n.*2084G>A
ENST00000697681.1:c.*2281G>A	ENSP00000513393.1:n.*2281G>A
ENST00000697683.1:c.*2056G>A	ENSP00000513395.1:n.*2056G>A
ENST00000697685.1:c.*1817G>A	ENSP00000513396.1:n.*1817G>A
ENST00000697686.1:c.*30G>A	ENSP00000513397.1:n.*30G>A
ENST00000697689.1:c.*1534G>A	ENSP00000513398.1:n.*1534G>A
ENST00000697690.1:c.*80G>A	ENSP00000513399.1:n.*80G>A
ENST00000697691.1:c.*1092G>A	ENSP00000513400.1:n.*1092G>A
ENST00000697692.1:c.*1132G>A	ENSP00000513401.1:n.*1132G>A
ENST00000697694.1:c.769G>A	ENSP00000513402.1:p.Glu257Lys
ENST00000697695.1:n.1727G>A
XM_006722001.2:c.1123G>A	XP_006722064.1:p.Glu375Lys
XM_006722001.4:c.1123G>A	XP_006722064.1:p.Glu375Lys
XM_006722002.2:c.*30G>A	XP_006722065.1:n.*30G>A
XM_006722002.4:c.*30G>A	XP_006722065.1:n.*30G>A
XM_006722004.2:c.772G>A	XP_006722067.1:p.Glu258Lys
XM_006722004.3:c.772G>A	XP_006722067.1:p.Glu258Lys
XM_006722005.2:c.772G>A	XP_006722068.1:p.Glu258Lys
XM_006722005.3:c.772G>A	XP_006722068.1:p.Glu258Lys
XM_011525092.1:c.772G>A	XP_011523394.1:p.Glu258Lys
XM_011525092.2:c.772G>A	XP_011523394.1:p.Glu258Lys
XM_011525093.1:c.772G>A	XP_011523395.1:p.Glu258Lys
XM_011525093.2:c.772G>A	XP_011523395.1:p.Glu258Lys
XM_011525094.1:c.772G>A	XP_011523396.1:p.Glu258Lys
XM_011525094.2:c.772G>A	XP_011523396.1:p.Glu258Lys
XM_017024914.1:c.769G>A	XP_016880403.1:p.Glu257Lys
XM_017024915.1:c.769G>A	XP_016880404.1:p.Glu257Lys
XM_017024916.1:c.769G>A	XP_016880405.1:p.Glu257Lys
XM_017024917.1:c.769G>A	XP_016880406.1:p.Glu257Lys
XM_017024918.2:c.769G>A	XP_016880407.1:p.Glu257Lys
XM_017024919.1:c.*30G>A	XP_016880408.1:n.*30G>A
XR_934513.1:n.1338G>A
XR_934513.3:n.1769G>A
XR_934886.1:n.149+3860C>T
XR_934886.2:n.149+3860C>T