Canonical Allele Identifier: CA2267819513
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703320A= , CM000679.2:g.58703320A= GRCh38
NC_000017.10:g.56780681A= , CM000679.1:g.56780681A= GRCh37
NC_000017.9:g.54135680A= NCBI36
NG_023199.1:g.15719A= , LRG_314:g.15719A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.345A= ENSP00000464056.2:p.Glu115=
ENST00000697677.1:n.1777A=
ENST00000697678.1:n.598A=
ENST00000697679.1:n.1770A=
ENST00000697680.1:c.*1560A= ENSP00000513392.1:n.*1560A=
ENST00000697681.1:c.*1712A= ENSP00000513393.1:n.*1712A=
ENST00000697683.1:c.*1560A= ENSP00000513395.1:n.*1560A=
ENST00000697684.1:n.756A=
ENST00000697685.1:c.*1393A= ENSP00000513396.1:n.*1393A=
ENST00000697686.1:c.345A= ENSP00000513397.1:p.Glu115=
ENST00000697687.1:n.575A=
ENST00000697688.1:n.742A=
ENST00000697689.1:c.*1232A= ENSP00000513398.1:n.*1232A=
ENST00000697690.1:c.696A= ENSP00000513399.1:p.Glu232=
ENST00000697691.1:c.*668A= ENSP00000513400.1:n.*668A=
ENST00000697692.1:c.*708A= ENSP00000513401.1:n.*708A=
ENST00000697694.1:c.345A= ENSP00000513402.1:p.Glu115=
ENST00000697695.1:n.1303A=
ENST00000337432.9:c.696A= MANE Select ENSP00000336701.4:p.Glu232=
ENST00000337432.8:c.696A= ENSP00000336701.4:p.Glu232=
ENST00000413590.5:c.334A=
ENST00000425173.5:c.492A= ENSP00000407282.1:p.Glu164=
ENST00000461271.5:c.345A= ENSP00000464056.1:p.Glu115=
ENST00000475762.5:c.*1399A= ENSP00000432421.1:n.*1399A=
ENST00000482007.5:c.*124A= ENSP00000433332.1:n.*124A=
ENST00000487525.5:c.*124A= ENSP00000431637.1:n.*124A=
ENST00000487921.5:n.608A=
ENST00000583539.5:c.696A= ENSP00000463121.1:p.Glu232=
ENST00000584617.5:c.418A=
NM_058216.2:c.696A= NP_478123.1:p.Glu232=
NR_103872.1:n.600A=
XM_006722001.2:c.696A= XP_006722064.1:p.Glu232=
XM_006722002.2:c.696A= XP_006722065.1:p.Glu232=
XM_006722004.2:c.345A= XP_006722067.1:p.Glu115=
XM_006722005.2:c.345A= XP_006722068.1:p.Glu115=
XM_011525092.1:c.345A= XP_011523394.1:p.Glu115=
XM_011525093.1:c.345A= XP_011523395.1:p.Glu115=
XM_011525094.1:c.345A= XP_011523396.1:p.Glu115=
XR_934513.1:n.769A=
XR_934514.1:n.769A=
XM_006722001.4:c.696A= XP_006722064.1:p.Glu232=
XM_006722002.4:c.696A= XP_006722065.1:p.Glu232=
XM_006722004.3:c.345A= XP_006722067.1:p.Glu115=
XM_006722005.3:c.345A= XP_006722068.1:p.Glu115=
XM_011525092.2:c.345A= XP_011523394.1:p.Glu115=
XM_011525093.2:c.345A= XP_011523395.1:p.Glu115=
XM_011525094.2:c.345A= XP_011523396.1:p.Glu115=
XM_017024914.1:c.345A= XP_016880403.1:p.Glu115=
XM_017024915.1:c.345A= XP_016880404.1:p.Glu115=
XM_017024916.1:c.345A= XP_016880405.1:p.Glu115=
XM_017024917.1:c.345A= XP_016880406.1:p.Glu115=
XM_017024918.2:c.345A= XP_016880407.1:p.Glu115=
XM_017024919.1:c.345A= XP_016880408.1:p.Glu115=
XR_934513.3:n.1200A=
XR_934514.3:n.1200A=
NM_058216.3:c.696A= MANE Select NP_478123.1:p.Glu232=
NR_103872.2:n.571A=