Canonical Allele Identifier: CA400366166
Community Standard Title: NM_058216.3(RAD51C):c.1065T>G (p.Cys355Trp)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734156T>G , CM000679.2:g.58734156T>G GRCh38
NC_000017.10:g.56811517T>G , CM000679.1:g.56811517T>G GRCh37
NC_000017.9:g.54166516T>G NCBI36
NG_023199.1:g.46555T>G , LRG_314:g.46555T>G

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1065T>G MANE Select NP_478123.1:p.Cys355Trp
ENST00000337432.9:c.1065T>G MANE Select ENSP00000336701.4:p.Cys355Trp
NM_058216.2:c.1065T>G NP_478123.1:p.Cys355Trp
NR_103872.1:n.969T>G
NR_103872.2:n.940T>G
ENST00000337432.8:c.1065T>G ENSP00000336701.4:p.Cys355Trp
ENST00000413590.5:c.706T>G
ENST00000461271.6:c.*1597T>G ENSP00000464056.2:n.*1597T>G
ENST00000461706.1:n.252T>G
ENST00000475762.5:c.*1701T>G ENSP00000432421.1:n.*1701T>G
ENST00000482007.5:c.*493T>G ENSP00000433332.1:n.*493T>G
ENST00000487525.5:c.*641T>G ENSP00000431637.1:n.*641T>G
ENST00000578151.1:n.278T>G
ENST00000581221.5:n.580T>G
ENST00000584804.1:c.299T>G ENSP00000463658.1:p.Val100Gly
ENST00000697680.1:c.*2029T>G ENSP00000513392.1:n.*2029T>G
ENST00000697681.1:c.*2226T>G ENSP00000513393.1:n.*2226T>G
ENST00000697683.1:c.*2001T>G ENSP00000513395.1:n.*2001T>G
ENST00000697685.1:c.*1762T>G ENSP00000513396.1:n.*1762T>G
ENST00000697686.1:c.836T>G ENSP00000513397.1:p.Val279Gly
ENST00000697689.1:c.*1479T>G ENSP00000513398.1:n.*1479T>G
ENST00000697690.1:c.*25T>G ENSP00000513399.1:n.*25T>G
ENST00000697691.1:c.*1037T>G ENSP00000513400.1:n.*1037T>G
ENST00000697692.1:c.*1077T>G ENSP00000513401.1:n.*1077T>G
ENST00000697694.1:c.714T>G ENSP00000513402.1:p.Cys238Trp
ENST00000697695.1:n.1672T>G
XM_006722001.2:c.1068T>G XP_006722064.1:p.Cys356Trp
XM_006722001.4:c.1068T>G XP_006722064.1:p.Cys356Trp
XM_006722002.2:c.1004T>G XP_006722065.1:p.Val335Gly
XM_006722002.4:c.1004T>G XP_006722065.1:p.Val335Gly
XM_006722004.2:c.717T>G XP_006722067.1:p.Cys239Trp
XM_006722004.3:c.717T>G XP_006722067.1:p.Cys239Trp
XM_006722005.2:c.717T>G XP_006722068.1:p.Cys239Trp
XM_006722005.3:c.717T>G XP_006722068.1:p.Cys239Trp
XM_011525092.1:c.717T>G XP_011523394.1:p.Cys239Trp
XM_011525092.2:c.717T>G XP_011523394.1:p.Cys239Trp
XM_011525093.1:c.717T>G XP_011523395.1:p.Cys239Trp
XM_011525093.2:c.717T>G XP_011523395.1:p.Cys239Trp
XM_011525094.1:c.717T>G XP_011523396.1:p.Cys239Trp
XM_011525094.2:c.717T>G XP_011523396.1:p.Cys239Trp
XM_017024914.1:c.714T>G XP_016880403.1:p.Cys238Trp
XM_017024915.1:c.714T>G XP_016880404.1:p.Cys238Trp
XM_017024916.1:c.714T>G XP_016880405.1:p.Cys238Trp
XM_017024917.1:c.714T>G XP_016880406.1:p.Cys238Trp
XM_017024918.2:c.714T>G XP_016880407.1:p.Cys238Trp
XM_017024919.1:c.653T>G XP_016880408.1:p.Val218Gly
XR_934513.1:n.1283T>G
XR_934513.3:n.1714T>G
XR_934514.1:n.1286T>G
XR_934514.3:n.1717T>G
XR_934886.1:n.149+3915A>C
XR_934886.2:n.149+3915A>C