Canonical Allele Identifier: CA168293

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58734187C>T , CM000679.2:g.58734187C>T	GRCh38
NC_000017.10:g.56811548C>T , CM000679.1:g.56811548C>T	GRCh37
NC_000017.9:g.54166547C>T	NCBI36
NG_023199.1:g.46586C>T , LRG_314:g.46586C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_058216.3:c.1096C>T MANE Select	NP_478123.1:p.Arg366Trp
ENST00000337432.9:c.1096C>T MANE Select	ENSP00000336701.4:p.Arg366Trp
NM_058216.2:c.1096C>T	NP_478123.1:p.Arg366Trp
NR_103872.1:n.1000C>T
NR_103872.2:n.971C>T
ENST00000337432.8:c.1096C>T	ENSP00000336701.4:p.Arg366Trp
ENST00000413590.5:c.737C>T
ENST00000461271.6:c.*1628C>T	ENSP00000464056.2:n.*1628C>T
ENST00000461706.1:n.283C>T
ENST00000475762.5:c.*1732C>T	ENSP00000432421.1:n.*1732C>T
ENST00000482007.5:c.*524C>T	ENSP00000433332.1:n.*524C>T
ENST00000487525.5:c.*672C>T	ENSP00000431637.1:n.*672C>T
ENST00000578151.1:n.309C>T
ENST00000581221.5:n.611C>T
ENST00000584804.1:c.330C>T	ENSP00000463658.1:n.330C>T
ENST00000697680.1:c.*2060C>T	ENSP00000513392.1:n.*2060C>T
ENST00000697681.1:c.*2257C>T	ENSP00000513393.1:n.*2257C>T
ENST00000697683.1:c.*2032C>T	ENSP00000513395.1:n.*2032C>T
ENST00000697685.1:c.*1793C>T	ENSP00000513396.1:n.*1793C>T
ENST00000697686.1:c.*6C>T	ENSP00000513397.1:n.*6C>T
ENST00000697689.1:c.*1510C>T	ENSP00000513398.1:n.*1510C>T
ENST00000697690.1:c.*56C>T	ENSP00000513399.1:n.*56C>T
ENST00000697691.1:c.*1068C>T	ENSP00000513400.1:n.*1068C>T
ENST00000697692.1:c.*1108C>T	ENSP00000513401.1:n.*1108C>T
ENST00000697694.1:c.745C>T	ENSP00000513402.1:p.Arg249Trp
ENST00000697695.1:n.1703C>T
XM_006722001.2:c.1099C>T	XP_006722064.1:p.Arg367Trp
XM_006722001.4:c.1099C>T	XP_006722064.1:p.Arg367Trp
XM_006722002.2:c.*6C>T	XP_006722065.1:n.*6C>T
XM_006722002.4:c.*6C>T	XP_006722065.1:n.*6C>T
XM_006722004.2:c.748C>T	XP_006722067.1:p.Arg250Trp
XM_006722004.3:c.748C>T	XP_006722067.1:p.Arg250Trp
XM_006722005.2:c.748C>T	XP_006722068.1:p.Arg250Trp
XM_006722005.3:c.748C>T	XP_006722068.1:p.Arg250Trp
XM_011525092.1:c.748C>T	XP_011523394.1:p.Arg250Trp
XM_011525092.2:c.748C>T	XP_011523394.1:p.Arg250Trp
XM_011525093.1:c.748C>T	XP_011523395.1:p.Arg250Trp
XM_011525093.2:c.748C>T	XP_011523395.1:p.Arg250Trp
XM_011525094.1:c.748C>T	XP_011523396.1:p.Arg250Trp
XM_011525094.2:c.748C>T	XP_011523396.1:p.Arg250Trp
XM_017024914.1:c.745C>T	XP_016880403.1:p.Arg249Trp
XM_017024915.1:c.745C>T	XP_016880404.1:p.Arg249Trp
XM_017024916.1:c.745C>T	XP_016880405.1:p.Arg249Trp
XM_017024917.1:c.745C>T	XP_016880406.1:p.Arg249Trp
XM_017024918.2:c.745C>T	XP_016880407.1:p.Arg249Trp
XM_017024919.1:c.*6C>T	XP_016880408.1:n.*6C>T
XR_934513.1:n.1314C>T
XR_934513.3:n.1745C>T
XR_934886.1:n.149+3884G>A
XR_934886.2:n.149+3884G>A