Canonical Allele Identifier: CA400366018

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58734139G>A , CM000679.2:g.58734139G>A	GRCh38
NC_000017.10:g.56811500G>A , CM000679.1:g.56811500G>A	GRCh37
NC_000017.9:g.54166499G>A	NCBI36
NG_023199.1:g.46538G>A , LRG_314:g.46538G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_058216.3:c.1048G>A MANE Select	NP_478123.1:p.Val350Ile
ENST00000337432.9:c.1048G>A MANE Select	ENSP00000336701.4:p.Val350Ile
NM_058216.2:c.1048G>A	NP_478123.1:p.Val350Ile
NR_103872.1:n.952G>A
NR_103872.2:n.923G>A
ENST00000337432.8:c.1048G>A	ENSP00000336701.4:p.Val350Ile
ENST00000413590.5:c.689G>A
ENST00000461271.6:c.*1580G>A	ENSP00000464056.2:n.*1580G>A
ENST00000461706.1:n.235G>A
ENST00000475762.5:c.*1684G>A	ENSP00000432421.1:n.*1684G>A
ENST00000482007.5:c.*476G>A	ENSP00000433332.1:n.*476G>A
ENST00000487525.5:c.*624G>A	ENSP00000431637.1:n.*624G>A
ENST00000578151.1:n.261G>A
ENST00000581221.5:n.563G>A
ENST00000584804.1:c.282G>A	ENSP00000463658.1:p.Leu94=
ENST00000697680.1:c.*2012G>A	ENSP00000513392.1:n.*2012G>A
ENST00000697681.1:c.*2209G>A	ENSP00000513393.1:n.*2209G>A
ENST00000697683.1:c.*1984G>A	ENSP00000513395.1:n.*1984G>A
ENST00000697685.1:c.*1745G>A	ENSP00000513396.1:n.*1745G>A
ENST00000697686.1:c.819G>A	ENSP00000513397.1:p.Leu273=
ENST00000697689.1:c.*1462G>A	ENSP00000513398.1:n.*1462G>A
ENST00000697690.1:c.*8G>A	ENSP00000513399.1:n.*8G>A
ENST00000697691.1:c.*1020G>A	ENSP00000513400.1:n.*1020G>A
ENST00000697692.1:c.*1060G>A	ENSP00000513401.1:n.*1060G>A
ENST00000697694.1:c.697G>A	ENSP00000513402.1:p.Val233Ile
ENST00000697695.1:n.1655G>A
XM_006722001.2:c.1051G>A	XP_006722064.1:p.Val351Ile
XM_006722001.4:c.1051G>A	XP_006722064.1:p.Val351Ile
XM_006722002.2:c.987G>A	XP_006722065.1:p.Leu329=
XM_006722002.4:c.987G>A	XP_006722065.1:p.Leu329=
XM_006722004.2:c.700G>A	XP_006722067.1:p.Val234Ile
XM_006722004.3:c.700G>A	XP_006722067.1:p.Val234Ile
XM_006722005.2:c.700G>A	XP_006722068.1:p.Val234Ile
XM_006722005.3:c.700G>A	XP_006722068.1:p.Val234Ile
XM_011525092.1:c.700G>A	XP_011523394.1:p.Val234Ile
XM_011525092.2:c.700G>A	XP_011523394.1:p.Val234Ile
XM_011525093.1:c.700G>A	XP_011523395.1:p.Val234Ile
XM_011525093.2:c.700G>A	XP_011523395.1:p.Val234Ile
XM_011525094.1:c.700G>A	XP_011523396.1:p.Val234Ile
XM_011525094.2:c.700G>A	XP_011523396.1:p.Val234Ile
XM_017024914.1:c.697G>A	XP_016880403.1:p.Val233Ile
XM_017024915.1:c.697G>A	XP_016880404.1:p.Val233Ile
XM_017024916.1:c.697G>A	XP_016880405.1:p.Val233Ile
XM_017024917.1:c.697G>A	XP_016880406.1:p.Val233Ile
XM_017024918.2:c.697G>A	XP_016880407.1:p.Val233Ile
XM_017024919.1:c.636G>A	XP_016880408.1:p.Leu212=
XR_934513.1:n.1266G>A
XR_934513.3:n.1697G>A
XR_934514.1:n.1269G>A
XR_934514.3:n.1700G>A
XR_934886.1:n.149+3932C>T
XR_934886.2:n.149+3932C>T