Canonical Allele Identifier: CA400341542
Community Standard Title: NM_058216.3(RAD51C):c.351A>C (p.Leu117Phe)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58695136A>C , CM000679.2:g.58695136A>C GRCh38
NC_000017.10:g.56772497A>C , CM000679.1:g.56772497A>C GRCh37
NC_000017.9:g.54127496A>C NCBI36
NG_023199.1:g.7535A>C , LRG_314:g.7535A>C
NG_047169.1:g.1944T>G

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.351A>C MANE Select NP_478123.1:p.Leu117Phe
ENST00000337432.9:c.351A>C MANE Select ENSP00000336701.4:p.Leu117Phe
NM_002876.3:c.351A>C NP_002867.1:p.Leu117Phe
NM_002876.4:c.351A>C NP_002867.1:p.Leu117Phe
NM_058216.2:c.351A>C NP_478123.1:p.Leu117Phe
NR_103872.1:n.422A>C
NR_103872.2:n.393A>C
NR_103873.1:n.319A>C
ENST00000337432.8:c.351A>C ENSP00000336701.4:p.Leu117Phe
ENST00000421782.3:c.351A>C ENSP00000391450.2:p.Leu117Phe
ENST00000425173.5:c.147A>C ENSP00000407282.1:p.Leu49Phe
ENST00000461271.5:c.-1A>C ENSP00000464056.1:n.-1A>C
ENST00000461271.6:c.-1A>C ENSP00000464056.2:n.-1A>C
ENST00000475762.5:c.*1054A>C ENSP00000432421.1:n.*1054A>C
ENST00000482007.5:c.351A>C ENSP00000433332.1:p.Leu117Phe
ENST00000486827.1:c.*1215A>C ENSP00000436761.1:n.*1215A>C
ENST00000487525.5:c.351A>C ENSP00000431637.1:p.Leu117Phe
ENST00000487921.5:n.263A>C
ENST00000583539.5:c.351A>C ENSP00000463121.1:p.Leu117Phe
ENST00000584617.5:c.127-1557A>C
ENST00000622327.4:c.87A>C ENSP00000482326.1:p.Leu29Phe
ENST00000697675.1:n.1445A>C
ENST00000697676.1:n.411A>C
ENST00000697677.1:n.1432A>C
ENST00000697678.1:n.253A>C
ENST00000697679.1:n.1425A>C
ENST00000697680.1:c.*1215A>C ENSP00000513392.1:n.*1215A>C
ENST00000697681.1:c.*1215A>C ENSP00000513393.1:n.*1215A>C
ENST00000697683.1:c.*1215A>C ENSP00000513395.1:n.*1215A>C
ENST00000697684.1:n.411A>C
ENST00000697685.1:c.*1215A>C ENSP00000513396.1:n.*1215A>C
ENST00000697686.1:c.-1A>C ENSP00000513397.1:n.-1A>C
ENST00000697687.1:n.397A>C
ENST00000697688.1:n.397A>C
ENST00000697689.1:c.*1054A>C ENSP00000513398.1:n.*1054A>C
ENST00000697690.1:c.351A>C ENSP00000513399.1:p.Leu117Phe
ENST00000697691.1:c.*323A>C ENSP00000513400.1:n.*323A>C
ENST00000697692.1:c.*363A>C ENSP00000513401.1:n.*363A>C
ENST00000697693.1:n.1126A>C
ENST00000697694.1:c.-1A>C ENSP00000513402.1:n.-1A>C
ENST00000697695.1:n.958A>C
XM_006722001.2:c.351A>C XP_006722064.1:p.Leu117Phe
XM_006722001.4:c.351A>C XP_006722064.1:p.Leu117Phe
XM_006722002.2:c.351A>C XP_006722065.1:p.Leu117Phe
XM_006722002.4:c.351A>C XP_006722065.1:p.Leu117Phe
XM_006722004.2:c.-1A>C XP_006722067.1:n.-1A>C
XM_006722004.3:c.-1A>C XP_006722067.1:n.-1A>C
XM_006722005.2:c.-1A>C XP_006722068.1:n.-1A>C
XM_006722005.3:c.-1A>C XP_006722068.1:n.-1A>C
XM_011525092.1:c.-1A>C XP_011523394.1:n.-1A>C
XM_011525092.2:c.-1A>C XP_011523394.1:n.-1A>C
XM_011525093.1:c.-1A>C XP_011523395.1:n.-1A>C
XM_011525093.2:c.-1A>C XP_011523395.1:n.-1A>C
XM_011525094.1:c.-1A>C XP_011523396.1:n.-1A>C
XM_011525094.2:c.-1A>C XP_011523396.1:n.-1A>C
XM_017024914.1:c.-1A>C XP_016880403.1:n.-1A>C
XM_017024915.1:c.-1A>C XP_016880404.1:n.-1A>C
XM_017024916.1:c.-1A>C XP_016880405.1:n.-1A>C
XM_017024917.1:c.-1A>C XP_016880406.1:n.-1A>C
XM_017024918.2:c.-1A>C XP_016880407.1:n.-1A>C
XM_017024919.1:c.-1A>C XP_016880408.1:n.-1A>C
XR_934513.1:n.424A>C
XR_934513.3:n.855A>C
XR_934514.1:n.424A>C
XR_934514.3:n.855A>C