Canonical Allele Identifier: CA2267814247
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58693016C= , CM000679.2:g.58693016C= GRCh38
NC_000017.10:g.56770377C= , CM000679.1:g.56770377C= GRCh37
NC_000017.9:g.54125376C= NCBI36
NG_023199.1:g.5415C= , LRG_314:g.5415C=
NG_047169.1:g.4064G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.-207+331C= ENSP00000464056.2:n.-207+331C=
ENST00000697675.1:n.444C=
ENST00000697676.1:n.205+228C=
ENST00000697677.1:n.431C=
ENST00000697678.1:n.47+384C=
ENST00000697679.1:n.424C=
ENST00000697680.1:c.*214C= ENSP00000513392.1:n.*214C=
ENST00000697681.1:c.*214C= ENSP00000513393.1:n.*214C=
ENST00000697683.1:c.*214C= ENSP00000513395.1:n.*214C=
ENST00000697684.1:n.205+228C=
ENST00000697685.1:c.*214C= ENSP00000513396.1:n.*214C=
ENST00000697686.1:c.-207+384C= ENSP00000513397.1:n.-207+384C=
ENST00000697687.1:n.191+228C=
ENST00000697688.1:n.191+228C=
ENST00000697689.1:c.*214C= ENSP00000513398.1:n.*214C=
ENST00000697690.1:c.145+228C= ENSP00000513399.1:n.145+228C=
ENST00000697691.1:c.42+331C= ENSP00000513400.1:n.42+331C=
ENST00000697692.1:c.*157+57C= ENSP00000513401.1:n.*157+57C=
ENST00000697693.1:n.286C=
ENST00000697694.1:c.-309C= ENSP00000513402.1:n.-309C=
ENST00000697695.1:n.90C=
ENST00000337432.9:c.145+228C= MANE Select ENSP00000336701.4:n.145+228C=
ENST00000337432.8:c.145+228C= ENSP00000336701.4:n.145+228C=
ENST00000421782.3:c.145+228C= ENSP00000391450.2:n.145+228C=
ENST00000461271.5:c.-207+331C= ENSP00000464056.1:n.-207+331C=
ENST00000475762.5:c.*214C= ENSP00000432421.1:n.*214C=
ENST00000476741.2:n.187+228C=
ENST00000482007.5:c.145+228C= ENSP00000433332.1:n.145+228C=
ENST00000486827.1:c.*214C= ENSP00000436761.1:n.*214C=
ENST00000487525.5:c.145+228C= ENSP00000431637.1:n.145+228C=
ENST00000487921.5:n.57+384C=
ENST00000583539.5:c.145+228C= ENSP00000463121.1:n.145+228C=
ENST00000584617.5:c.126+228C=
NM_002876.3:c.145+228C= NP_002867.1:n.145+228C=
NM_058216.2:c.145+228C= NP_478123.1:n.145+228C=
NR_103872.1:n.216+228C=
NR_103873.1:n.113+331C=
XM_006722001.2:c.145+228C= XP_006722064.1:n.145+228C=
XM_006722002.2:c.145+228C= XP_006722065.1:n.145+228C=
XM_006722004.2:c.-207+331C= XP_006722067.1:n.-207+331C=
XM_006722005.2:c.-207+384C= XP_006722068.1:n.-207+384C=
XM_011525092.1:c.-507+331C= XP_011523394.1:n.-507+331C=
XM_011525093.1:c.-668+331C= XP_011523395.1:n.-668+331C=
XM_011525094.1:c.-207+57C= XP_011523396.1:n.-207+57C=
XR_934513.1:n.218+228C=
XR_934514.1:n.218+228C=
XM_006722001.4:c.145+228C= XP_006722064.1:n.145+228C=
XM_006722002.4:c.145+228C= XP_006722065.1:n.145+228C=
XM_006722004.3:c.-207+331C= XP_006722067.1:n.-207+331C=
XM_006722005.3:c.-207+384C= XP_006722068.1:n.-207+384C=
XM_011525092.2:c.-507+331C= XP_011523394.1:n.-507+331C=
XM_011525093.2:c.-668+331C= XP_011523395.1:n.-668+331C=
XM_011525094.2:c.-207+57C= XP_011523396.1:n.-207+57C=
XM_017024914.1:c.-207+331C= XP_016880403.1:n.-207+331C=
XM_017024916.1:c.-507+331C= XP_016880405.1:n.-507+331C=
XM_017024917.1:c.-207+384C= XP_016880406.1:n.-207+384C=
XM_017024918.2:c.-207+57C= XP_016880407.1:n.-207+57C=
XM_017024919.1:c.-668+331C= XP_016880408.1:n.-668+331C=
XR_934513.3:n.649+228C=
XR_934514.3:n.649+228C=
NM_058216.3:c.145+228C= MANE Select NP_478123.1:n.145+228C=
NR_103872.2:n.187+228C=
NM_002876.4:c.145+228C= NP_002867.1:n.145+228C=