Canonical Allele Identifier: CA168223
Community Standard Title: NM_058216.3(RAD51C):c.1063T>C (p.Cys355Arg)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734154T>C , CM000679.2:g.58734154T>C GRCh38
NC_000017.10:g.56811515T>C , CM000679.1:g.56811515T>C GRCh37
NC_000017.9:g.54166514T>C NCBI36
NG_023199.1:g.46553T>C , LRG_314:g.46553T>C

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1063T>C MANE Select NP_478123.1:p.Cys355Arg
ENST00000337432.9:c.1063T>C MANE Select ENSP00000336701.4:p.Cys355Arg
NM_058216.2:c.1063T>C NP_478123.1:p.Cys355Arg
NR_103872.1:n.967T>C
NR_103872.2:n.938T>C
ENST00000337432.8:c.1063T>C ENSP00000336701.4:p.Cys355Arg
ENST00000413590.5:c.704T>C
ENST00000461271.6:c.*1595T>C ENSP00000464056.2:n.*1595T>C
ENST00000461706.1:n.250T>C
ENST00000475762.5:c.*1699T>C ENSP00000432421.1:n.*1699T>C
ENST00000482007.5:c.*491T>C ENSP00000433332.1:n.*491T>C
ENST00000487525.5:c.*639T>C ENSP00000431637.1:n.*639T>C
ENST00000578151.1:n.276T>C
ENST00000581221.5:n.578T>C
ENST00000584804.1:c.297T>C ENSP00000463658.1:p.His99=
ENST00000697680.1:c.*2027T>C ENSP00000513392.1:n.*2027T>C
ENST00000697681.1:c.*2224T>C ENSP00000513393.1:n.*2224T>C
ENST00000697683.1:c.*1999T>C ENSP00000513395.1:n.*1999T>C
ENST00000697685.1:c.*1760T>C ENSP00000513396.1:n.*1760T>C
ENST00000697686.1:c.834T>C ENSP00000513397.1:p.His278=
ENST00000697689.1:c.*1477T>C ENSP00000513398.1:n.*1477T>C
ENST00000697690.1:c.*23T>C ENSP00000513399.1:n.*23T>C
ENST00000697691.1:c.*1035T>C ENSP00000513400.1:n.*1035T>C
ENST00000697692.1:c.*1075T>C ENSP00000513401.1:n.*1075T>C
ENST00000697694.1:c.712T>C ENSP00000513402.1:p.Cys238Arg
ENST00000697695.1:n.1670T>C
XM_006722001.2:c.1066T>C XP_006722064.1:p.Cys356Arg
XM_006722001.4:c.1066T>C XP_006722064.1:p.Cys356Arg
XM_006722002.2:c.1002T>C XP_006722065.1:p.His334=
XM_006722002.4:c.1002T>C XP_006722065.1:p.His334=
XM_006722004.2:c.715T>C XP_006722067.1:p.Cys239Arg
XM_006722004.3:c.715T>C XP_006722067.1:p.Cys239Arg
XM_006722005.2:c.715T>C XP_006722068.1:p.Cys239Arg
XM_006722005.3:c.715T>C XP_006722068.1:p.Cys239Arg
XM_011525092.1:c.715T>C XP_011523394.1:p.Cys239Arg
XM_011525092.2:c.715T>C XP_011523394.1:p.Cys239Arg
XM_011525093.1:c.715T>C XP_011523395.1:p.Cys239Arg
XM_011525093.2:c.715T>C XP_011523395.1:p.Cys239Arg
XM_011525094.1:c.715T>C XP_011523396.1:p.Cys239Arg
XM_011525094.2:c.715T>C XP_011523396.1:p.Cys239Arg
XM_017024914.1:c.712T>C XP_016880403.1:p.Cys238Arg
XM_017024915.1:c.712T>C XP_016880404.1:p.Cys238Arg
XM_017024916.1:c.712T>C XP_016880405.1:p.Cys238Arg
XM_017024917.1:c.712T>C XP_016880406.1:p.Cys238Arg
XM_017024918.2:c.712T>C XP_016880407.1:p.Cys238Arg
XM_017024919.1:c.651T>C XP_016880408.1:p.His217=
XR_934513.1:n.1281T>C
XR_934513.3:n.1712T>C
XR_934514.1:n.1284T>C
XR_934514.3:n.1715T>C
XR_934886.1:n.149+3917A>G
XR_934886.2:n.149+3917A>G