Canonical Allele Identifier: CA166555

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58732486T>G , CM000679.2:g.58732486T>G	GRCh38
NC_000017.10:g.56809847T>G , CM000679.1:g.56809847T>G	GRCh37
NC_000017.9:g.54164846T>G	NCBI36
NG_023199.1:g.44885T>G , LRG_314:g.44885T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.617T>G	ENSP00000464056.2:p.Leu206Trp
ENST00000697680.1:c.*1932T>G	ENSP00000513392.1:n.*1932T>G
ENST00000697681.1:c.*2129T>G	ENSP00000513393.1:n.*2129T>G
ENST00000697683.1:c.*1904T>G	ENSP00000513395.1:n.*1904T>G
ENST00000697685.1:c.*1665T>G	ENSP00000513396.1:n.*1665T>G
ENST00000697686.1:c.739T>G	ENSP00000513397.1:p.Trp247Gly
ENST00000697689.1:c.*1441-1632T>G	ENSP00000513398.1:n.*1441-1632T>G
ENST00000697690.1:c.905-1632T>G	ENSP00000513399.1:n.905-1632T>G
ENST00000697691.1:c.*940T>G	ENSP00000513400.1:n.*940T>G
ENST00000697692.1:c.*980T>G	ENSP00000513401.1:n.*980T>G
ENST00000697694.1:c.617T>G	ENSP00000513402.1:p.Leu206Trp
ENST00000697695.1:n.1575T>G
ENST00000337432.9:c.968T>G MANE Select	ENSP00000336701.4:p.Leu323Trp
ENST00000337432.8:c.968T>G	ENSP00000336701.4:p.Leu323Trp
ENST00000413590.5:c.609T>G
ENST00000461706.1:n.155T>G
ENST00000475762.5:c.*1604T>G	ENSP00000432421.1:n.*1604T>G
ENST00000482007.5:c.*396T>G	ENSP00000433332.1:n.*396T>G
ENST00000487525.5:c.*544T>G	ENSP00000431637.1:n.*544T>G
ENST00000578151.1:n.240-1632T>G
ENST00000581221.5:n.483T>G
ENST00000583539.5:c.968T>G	ENSP00000463121.1:p.Leu323Trp
ENST00000584617.5:c.690T>G
ENST00000584804.1:c.202T>G	ENSP00000463658.1:p.Trp68Gly
NM_058216.2:c.968T>G	NP_478123.1:p.Leu323Trp
NR_103872.1:n.872T>G
XM_006722001.2:c.971T>G	XP_006722064.1:p.Leu324Trp
XM_006722002.2:c.907T>G	XP_006722065.1:p.Trp303Gly
XM_006722004.2:c.620T>G	XP_006722067.1:p.Leu207Trp
XM_006722005.2:c.620T>G	XP_006722068.1:p.Leu207Trp
XM_011525092.1:c.620T>G	XP_011523394.1:p.Leu207Trp
XM_011525093.1:c.620T>G	XP_011523395.1:p.Leu207Trp
XM_011525094.1:c.620T>G	XP_011523396.1:p.Leu207Trp
XR_934513.1:n.1186T>G
XR_934514.1:n.1189T>G
XR_934886.1:n.149+5585A>C
XM_006722001.4:c.971T>G	XP_006722064.1:p.Leu324Trp
XM_006722002.4:c.907T>G	XP_006722065.1:p.Trp303Gly
XM_006722004.3:c.620T>G	XP_006722067.1:p.Leu207Trp
XM_006722005.3:c.620T>G	XP_006722068.1:p.Leu207Trp
XM_011525092.2:c.620T>G	XP_011523394.1:p.Leu207Trp
XM_011525093.2:c.620T>G	XP_011523395.1:p.Leu207Trp
XM_011525094.2:c.620T>G	XP_011523396.1:p.Leu207Trp
XM_017024914.1:c.617T>G	XP_016880403.1:p.Leu206Trp
XM_017024915.1:c.617T>G	XP_016880404.1:p.Leu206Trp
XM_017024916.1:c.617T>G	XP_016880405.1:p.Leu206Trp
XM_017024917.1:c.617T>G	XP_016880406.1:p.Leu206Trp
XM_017024918.2:c.617T>G	XP_016880407.1:p.Leu206Trp
XM_017024919.1:c.556T>G	XP_016880408.1:p.Trp186Gly
XR_934513.3:n.1617T>G
XR_934514.3:n.1620T>G
XR_934886.2:n.149+5585A>C
NM_058216.3:c.968T>G MANE Select	NP_478123.1:p.Leu323Trp
NR_103872.2:n.843T>G