Canonical Allele Identifier: CA400359424

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58720764A>G , CM000679.2:g.58720764A>G	GRCh38
NC_000017.10:g.56798125A>G , CM000679.1:g.56798125A>G	GRCh37
NC_000017.9:g.54153124A>G	NCBI36
NG_023199.1:g.33163A>G , LRG_314:g.33163A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_058216.3:c.856A>G MANE Select	NP_478123.1:p.Met286Val
ENST00000337432.9:c.856A>G MANE Select	ENSP00000336701.4:p.Met286Val
NM_058216.2:c.856A>G	NP_478123.1:p.Met286Val
NR_103872.1:n.760A>G
NR_103872.2:n.731A>G
ENST00000337432.8:c.856A>G	ENSP00000336701.4:p.Met286Val
ENST00000413590.5:c.494A>G
ENST00000461271.6:c.505A>G	ENSP00000464056.2:p.Met169Val
ENST00000475762.5:c.*1541-3276A>G	ENSP00000432421.1:n.*1541-3276A>G
ENST00000482007.5:c.*284A>G	ENSP00000433332.1:n.*284A>G
ENST00000487525.5:c.*429A>G	ENSP00000431637.1:n.*429A>G
ENST00000578151.1:n.191A>G
ENST00000581221.5:n.371A>G
ENST00000583539.5:c.856A>G	ENSP00000463121.1:p.Met286Val
ENST00000584617.5:c.578A>G
ENST00000584804.1:c.151A>G	ENSP00000463658.1:p.Met51Val
ENST00000697678.1:n.758A>G
ENST00000697679.1:n.1930A>G
ENST00000697680.1:c.*1820A>G	ENSP00000513392.1:n.*1820A>G
ENST00000697681.1:c.*2017A>G	ENSP00000513393.1:n.*2017A>G
ENST00000697683.1:c.*1720A>G	ENSP00000513395.1:n.*1720A>G
ENST00000697684.1:n.916A>G
ENST00000697685.1:c.*1553A>G	ENSP00000513396.1:n.*1553A>G
ENST00000697686.1:c.505A>G	ENSP00000513397.1:p.Met169Val
ENST00000697687.1:n.735A>G
ENST00000697688.1:n.902A>G
ENST00000697689.1:c.*1392A>G	ENSP00000513398.1:n.*1392A>G
ENST00000697690.1:c.856A>G	ENSP00000513399.1:p.Met286Val
ENST00000697691.1:c.*828A>G	ENSP00000513400.1:n.*828A>G
ENST00000697692.1:c.*868A>G	ENSP00000513401.1:n.*868A>G
ENST00000697694.1:c.505A>G	ENSP00000513402.1:p.Met169Val
ENST00000697695.1:n.1463A>G
XM_006722001.2:c.856A>G	XP_006722064.1:p.Met286Val
XM_006722001.4:c.856A>G	XP_006722064.1:p.Met286Val
XM_006722002.2:c.856A>G	XP_006722065.1:p.Met286Val
XM_006722002.4:c.856A>G	XP_006722065.1:p.Met286Val
XM_006722004.2:c.505A>G	XP_006722067.1:p.Met169Val
XM_006722004.3:c.505A>G	XP_006722067.1:p.Met169Val
XM_006722005.2:c.505A>G	XP_006722068.1:p.Met169Val
XM_006722005.3:c.505A>G	XP_006722068.1:p.Met169Val
XM_011525092.1:c.505A>G	XP_011523394.1:p.Met169Val
XM_011525092.2:c.505A>G	XP_011523394.1:p.Met169Val
XM_011525093.1:c.505A>G	XP_011523395.1:p.Met169Val
XM_011525093.2:c.505A>G	XP_011523395.1:p.Met169Val
XM_011525094.1:c.505A>G	XP_011523396.1:p.Met169Val
XM_011525094.2:c.505A>G	XP_011523396.1:p.Met169Val
XM_017024914.1:c.505A>G	XP_016880403.1:p.Met169Val
XM_017024915.1:c.505A>G	XP_016880404.1:p.Met169Val
XM_017024916.1:c.505A>G	XP_016880405.1:p.Met169Val
XM_017024917.1:c.505A>G	XP_016880406.1:p.Met169Val
XM_017024918.2:c.505A>G	XP_016880407.1:p.Met169Val
XM_017024919.1:c.505A>G	XP_016880408.1:p.Met169Val
XR_934513.1:n.1074A>G
XR_934513.3:n.1505A>G
XR_934514.1:n.1074A>G
XR_934514.3:n.1505A>G