Canonical Allele Identifier: CA400365871

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58734124G>A , CM000679.2:g.58734124G>A	GRCh38
NC_000017.10:g.56811485G>A , CM000679.1:g.56811485G>A	GRCh37
NC_000017.9:g.54166484G>A	NCBI36
NG_023199.1:g.46523G>A , LRG_314:g.46523G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_058216.3:c.1033G>A MANE Select	NP_478123.1:p.Gly345Arg
ENST00000337432.9:c.1033G>A MANE Select	ENSP00000336701.4:p.Gly345Arg
NM_058216.2:c.1033G>A	NP_478123.1:p.Gly345Arg
NR_103872.1:n.937G>A
NR_103872.2:n.908G>A
ENST00000337432.8:c.1033G>A	ENSP00000336701.4:p.Gly345Arg
ENST00000413590.5:c.674G>A
ENST00000461271.6:c.*1565G>A	ENSP00000464056.2:n.*1565G>A
ENST00000461706.1:n.220G>A
ENST00000475762.5:c.*1669G>A	ENSP00000432421.1:n.*1669G>A
ENST00000482007.5:c.*461G>A	ENSP00000433332.1:n.*461G>A
ENST00000487525.5:c.*609G>A	ENSP00000431637.1:n.*609G>A
ENST00000578151.1:n.246G>A
ENST00000581221.5:n.548G>A
ENST00000584804.1:c.267G>A	ENSP00000463658.1:p.Arg89=
ENST00000697680.1:c.*1997G>A	ENSP00000513392.1:n.*1997G>A
ENST00000697681.1:c.*2194G>A	ENSP00000513393.1:n.*2194G>A
ENST00000697683.1:c.*1969G>A	ENSP00000513395.1:n.*1969G>A
ENST00000697685.1:c.*1730G>A	ENSP00000513396.1:n.*1730G>A
ENST00000697686.1:c.804G>A	ENSP00000513397.1:p.Arg268=
ENST00000697689.1:c.*1447G>A	ENSP00000513398.1:n.*1447G>A
ENST00000697690.1:c.911G>A	ENSP00000513399.1:p.Gly304Glu
ENST00000697691.1:c.*1005G>A	ENSP00000513400.1:n.*1005G>A
ENST00000697692.1:c.*1045G>A	ENSP00000513401.1:n.*1045G>A
ENST00000697694.1:c.682G>A	ENSP00000513402.1:p.Gly228Arg
ENST00000697695.1:n.1640G>A
XM_006722001.2:c.1036G>A	XP_006722064.1:p.Gly346Arg
XM_006722001.4:c.1036G>A	XP_006722064.1:p.Gly346Arg
XM_006722002.2:c.972G>A	XP_006722065.1:p.Arg324=
XM_006722002.4:c.972G>A	XP_006722065.1:p.Arg324=
XM_006722004.2:c.685G>A	XP_006722067.1:p.Gly229Arg
XM_006722004.3:c.685G>A	XP_006722067.1:p.Gly229Arg
XM_006722005.2:c.685G>A	XP_006722068.1:p.Gly229Arg
XM_006722005.3:c.685G>A	XP_006722068.1:p.Gly229Arg
XM_011525092.1:c.685G>A	XP_011523394.1:p.Gly229Arg
XM_011525092.2:c.685G>A	XP_011523394.1:p.Gly229Arg
XM_011525093.1:c.685G>A	XP_011523395.1:p.Gly229Arg
XM_011525093.2:c.685G>A	XP_011523395.1:p.Gly229Arg
XM_011525094.1:c.685G>A	XP_011523396.1:p.Gly229Arg
XM_011525094.2:c.685G>A	XP_011523396.1:p.Gly229Arg
XM_017024914.1:c.682G>A	XP_016880403.1:p.Gly228Arg
XM_017024915.1:c.682G>A	XP_016880404.1:p.Gly228Arg
XM_017024916.1:c.682G>A	XP_016880405.1:p.Gly228Arg
XM_017024917.1:c.682G>A	XP_016880406.1:p.Gly228Arg
XM_017024918.2:c.682G>A	XP_016880407.1:p.Gly228Arg
XM_017024919.1:c.621G>A	XP_016880408.1:p.Arg207=
XR_934513.1:n.1251G>A
XR_934513.3:n.1682G>A
XR_934514.1:n.1254G>A
XR_934514.3:n.1685G>A
XR_934886.1:n.149+3947C>T
XR_934886.2:n.149+3947C>T