Canonical Allele Identifier: CA2267815376
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58695181A= , CM000679.2:g.58695181A= GRCh38
NC_000017.10:g.56772542A= , CM000679.1:g.56772542A= GRCh37
NC_000017.9:g.54127541A= NCBI36
NG_023199.1:g.7580A= , LRG_314:g.7580A=
NG_047169.1:g.1899T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.45A= ENSP00000464056.2:p.Thr15=
ENST00000697675.1:n.1490A=
ENST00000697676.1:n.456A=
ENST00000697677.1:n.1477A=
ENST00000697678.1:n.298A=
ENST00000697679.1:n.1470A=
ENST00000697680.1:c.*1260A= ENSP00000513392.1:n.*1260A=
ENST00000697681.1:c.*1260A= ENSP00000513393.1:n.*1260A=
ENST00000697683.1:c.*1260A= ENSP00000513395.1:n.*1260A=
ENST00000697684.1:n.456A=
ENST00000697685.1:c.*1260A= ENSP00000513396.1:n.*1260A=
ENST00000697686.1:c.45A= ENSP00000513397.1:p.Thr15=
ENST00000697687.1:n.442A=
ENST00000697688.1:n.442A=
ENST00000697689.1:c.*1099A= ENSP00000513398.1:n.*1099A=
ENST00000697690.1:c.396A= ENSP00000513399.1:p.Thr132=
ENST00000697691.1:c.*368A= ENSP00000513400.1:n.*368A=
ENST00000697692.1:c.*408A= ENSP00000513401.1:n.*408A=
ENST00000697693.1:n.1171A=
ENST00000697694.1:c.45A= ENSP00000513402.1:p.Thr15=
ENST00000697695.1:n.1003A=
ENST00000337432.9:c.396A= MANE Select ENSP00000336701.4:p.Thr132=
ENST00000337432.8:c.396A= ENSP00000336701.4:p.Thr132=
ENST00000413590.5:c.34A=
ENST00000421782.3:c.396A= ENSP00000391450.2:p.Thr132=
ENST00000425173.5:c.192A= ENSP00000407282.1:p.Thr64=
ENST00000461271.5:c.45A= ENSP00000464056.1:p.Thr15=
ENST00000475762.5:c.*1099A= ENSP00000432421.1:n.*1099A=
ENST00000482007.5:c.396A= ENSP00000433332.1:p.Thr132=
ENST00000486827.1:c.*1260A= ENSP00000436761.1:n.*1260A=
ENST00000487525.5:c.396A= ENSP00000431637.1:p.Thr132=
ENST00000487921.5:n.308A=
ENST00000583539.5:c.396A= ENSP00000463121.1:p.Thr132=
ENST00000584617.5:c.127-1512A=
ENST00000622327.4:c.132A= ENSP00000482326.1:p.Thr44=
NM_002876.3:c.396A= NP_002867.1:p.Thr132=
NM_058216.2:c.396A= NP_478123.1:p.Thr132=
NR_103872.1:n.467A=
NR_103873.1:n.364A=
XM_006722001.2:c.396A= XP_006722064.1:p.Thr132=
XM_006722002.2:c.396A= XP_006722065.1:p.Thr132=
XM_006722004.2:c.45A= XP_006722067.1:p.Thr15=
XM_006722005.2:c.45A= XP_006722068.1:p.Thr15=
XM_011525092.1:c.45A= XP_011523394.1:p.Thr15=
XM_011525093.1:c.45A= XP_011523395.1:p.Thr15=
XM_011525094.1:c.45A= XP_011523396.1:p.Thr15=
XR_934513.1:n.469A=
XR_934514.1:n.469A=
XM_006722001.4:c.396A= XP_006722064.1:p.Thr132=
XM_006722002.4:c.396A= XP_006722065.1:p.Thr132=
XM_006722004.3:c.45A= XP_006722067.1:p.Thr15=
XM_006722005.3:c.45A= XP_006722068.1:p.Thr15=
XM_011525092.2:c.45A= XP_011523394.1:p.Thr15=
XM_011525093.2:c.45A= XP_011523395.1:p.Thr15=
XM_011525094.2:c.45A= XP_011523396.1:p.Thr15=
XM_017024914.1:c.45A= XP_016880403.1:p.Thr15=
XM_017024915.1:c.45A= XP_016880404.1:p.Thr15=
XM_017024916.1:c.45A= XP_016880405.1:p.Thr15=
XM_017024917.1:c.45A= XP_016880406.1:p.Thr15=
XM_017024918.2:c.45A= XP_016880407.1:p.Thr15=
XM_017024919.1:c.45A= XP_016880408.1:p.Thr15=
XR_934513.3:n.900A=
XR_934514.3:n.900A=
NM_058216.3:c.396A= MANE Select NP_478123.1:p.Thr132=
NR_103872.2:n.438A=
NM_002876.4:c.396A= NP_002867.1:p.Thr132=