Canonical Allele Identifier: CA400359615
Community Standard Title: NM_058216.3(RAD51C):c.875G>A (p.Arg292Lys)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58720783G>A , CM000679.2:g.58720783G>A GRCh38
NC_000017.10:g.56798144G>A , CM000679.1:g.56798144G>A GRCh37
NC_000017.9:g.54153143G>A NCBI36
NG_023199.1:g.33182G>A , LRG_314:g.33182G>A

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.875G>A MANE Select NP_478123.1:p.Arg292Lys
ENST00000337432.9:c.875G>A MANE Select ENSP00000336701.4:p.Arg292Lys
NM_058216.2:c.875G>A NP_478123.1:p.Arg292Lys
NR_103872.1:n.779G>A
NR_103872.2:n.750G>A
ENST00000337432.8:c.875G>A ENSP00000336701.4:p.Arg292Lys
ENST00000413590.5:c.513G>A
ENST00000461271.6:c.524G>A ENSP00000464056.2:p.Arg175Lys
ENST00000475762.5:c.*1541-3257G>A ENSP00000432421.1:n.*1541-3257G>A
ENST00000482007.5:c.*303G>A ENSP00000433332.1:n.*303G>A
ENST00000487525.5:c.*448G>A ENSP00000431637.1:n.*448G>A
ENST00000578151.1:n.210G>A
ENST00000581221.5:n.390G>A
ENST00000583539.5:c.875G>A ENSP00000463121.1:p.Arg292Lys
ENST00000584617.5:c.597G>A
ENST00000584804.1:c.170G>A ENSP00000463658.1:p.Arg57Lys
ENST00000697678.1:n.777G>A
ENST00000697679.1:n.1949G>A
ENST00000697680.1:c.*1839G>A ENSP00000513392.1:n.*1839G>A
ENST00000697681.1:c.*2036G>A ENSP00000513393.1:n.*2036G>A
ENST00000697683.1:c.*1739G>A ENSP00000513395.1:n.*1739G>A
ENST00000697684.1:n.935G>A
ENST00000697685.1:c.*1572G>A ENSP00000513396.1:n.*1572G>A
ENST00000697686.1:c.524G>A ENSP00000513397.1:p.Arg175Lys
ENST00000697687.1:n.754G>A
ENST00000697688.1:n.921G>A
ENST00000697689.1:c.*1411G>A ENSP00000513398.1:n.*1411G>A
ENST00000697690.1:c.875G>A ENSP00000513399.1:p.Arg292Lys
ENST00000697691.1:c.*847G>A ENSP00000513400.1:n.*847G>A
ENST00000697692.1:c.*887G>A ENSP00000513401.1:n.*887G>A
ENST00000697694.1:c.524G>A ENSP00000513402.1:p.Arg175Lys
ENST00000697695.1:n.1482G>A
XM_006722001.2:c.875G>A XP_006722064.1:p.Arg292Lys
XM_006722001.4:c.875G>A XP_006722064.1:p.Arg292Lys
XM_006722002.2:c.875G>A XP_006722065.1:p.Arg292Lys
XM_006722002.4:c.875G>A XP_006722065.1:p.Arg292Lys
XM_006722004.2:c.524G>A XP_006722067.1:p.Arg175Lys
XM_006722004.3:c.524G>A XP_006722067.1:p.Arg175Lys
XM_006722005.2:c.524G>A XP_006722068.1:p.Arg175Lys
XM_006722005.3:c.524G>A XP_006722068.1:p.Arg175Lys
XM_011525092.1:c.524G>A XP_011523394.1:p.Arg175Lys
XM_011525092.2:c.524G>A XP_011523394.1:p.Arg175Lys
XM_011525093.1:c.524G>A XP_011523395.1:p.Arg175Lys
XM_011525093.2:c.524G>A XP_011523395.1:p.Arg175Lys
XM_011525094.1:c.524G>A XP_011523396.1:p.Arg175Lys
XM_011525094.2:c.524G>A XP_011523396.1:p.Arg175Lys
XM_017024914.1:c.524G>A XP_016880403.1:p.Arg175Lys
XM_017024915.1:c.524G>A XP_016880404.1:p.Arg175Lys
XM_017024916.1:c.524G>A XP_016880405.1:p.Arg175Lys
XM_017024917.1:c.524G>A XP_016880406.1:p.Arg175Lys
XM_017024918.2:c.524G>A XP_016880407.1:p.Arg175Lys
XM_017024919.1:c.524G>A XP_016880408.1:p.Arg175Lys
XR_934513.1:n.1093G>A
XR_934513.3:n.1524G>A
XR_934514.1:n.1093G>A
XR_934514.3:n.1524G>A