Canonical Allele Identifier: CA2267814312
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58693134A= , CM000679.2:g.58693134A= GRCh38
NC_000017.10:g.56770495A= , CM000679.1:g.56770495A= GRCh37
NC_000017.9:g.54125494A= NCBI36
NG_023199.1:g.5533A= , LRG_314:g.5533A=
NG_047169.1:g.3946T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.-207+449A= ENSP00000464056.2:n.-207+449A=
ENST00000697675.1:n.562A=
ENST00000697676.1:n.205+346A=
ENST00000697677.1:n.549A=
ENST00000697678.1:n.47+502A=
ENST00000697679.1:n.542A=
ENST00000697680.1:c.*332A= ENSP00000513392.1:n.*332A=
ENST00000697681.1:c.*332A= ENSP00000513393.1:n.*332A=
ENST00000697683.1:c.*332A= ENSP00000513395.1:n.*332A=
ENST00000697684.1:n.205+346A=
ENST00000697685.1:c.*332A= ENSP00000513396.1:n.*332A=
ENST00000697686.1:c.-207+502A= ENSP00000513397.1:n.-207+502A=
ENST00000697687.1:n.191+346A=
ENST00000697688.1:n.191+346A=
ENST00000697689.1:c.*332A= ENSP00000513398.1:n.*332A=
ENST00000697690.1:c.145+346A= ENSP00000513399.1:n.145+346A=
ENST00000697691.1:c.43-217A= ENSP00000513400.1:n.43-217A=
ENST00000697692.1:c.*157+175A= ENSP00000513401.1:n.*157+175A=
ENST00000697693.1:n.404A=
ENST00000697694.1:c.-207+16A= ENSP00000513402.1:n.-207+16A=
ENST00000697695.1:n.208A=
ENST00000337432.9:c.145+346A= MANE Select ENSP00000336701.4:n.145+346A=
ENST00000337432.8:c.145+346A= ENSP00000336701.4:n.145+346A=
ENST00000421782.3:c.145+346A= ENSP00000391450.2:n.145+346A=
ENST00000461271.5:c.-207+449A= ENSP00000464056.1:n.-207+449A=
ENST00000475762.5:c.*332A= ENSP00000432421.1:n.*332A=
ENST00000476741.2:n.188-217A=
ENST00000482007.5:c.145+346A= ENSP00000433332.1:n.145+346A=
ENST00000486827.1:c.*332A= ENSP00000436761.1:n.*332A=
ENST00000487525.5:c.145+346A= ENSP00000431637.1:n.145+346A=
ENST00000487921.5:n.57+502A=
ENST00000583539.5:c.145+346A= ENSP00000463121.1:n.145+346A=
ENST00000584617.5:c.126+346A=
NM_002876.3:c.145+346A= NP_002867.1:n.145+346A=
NM_058216.2:c.145+346A= NP_478123.1:n.145+346A=
NR_103872.1:n.216+346A=
NR_103873.1:n.113+449A=
XM_006722001.2:c.145+346A= XP_006722064.1:n.145+346A=
XM_006722002.2:c.145+346A= XP_006722065.1:n.145+346A=
XM_006722004.2:c.-207+449A= XP_006722067.1:n.-207+449A=
XM_006722005.2:c.-207+502A= XP_006722068.1:n.-207+502A=
XM_011525092.1:c.-506-217A= XP_011523394.1:n.-506-217A=
XM_011525093.1:c.-667-217A= XP_011523395.1:n.-667-217A=
XM_011525094.1:c.-207+175A= XP_011523396.1:n.-207+175A=
XR_934513.1:n.218+346A=
XR_934514.1:n.218+346A=
XM_006722001.4:c.145+346A= XP_006722064.1:n.145+346A=
XM_006722002.4:c.145+346A= XP_006722065.1:n.145+346A=
XM_006722004.3:c.-207+449A= XP_006722067.1:n.-207+449A=
XM_006722005.3:c.-207+502A= XP_006722068.1:n.-207+502A=
XM_011525092.2:c.-506-217A= XP_011523394.1:n.-506-217A=
XM_011525093.2:c.-667-217A= XP_011523395.1:n.-667-217A=
XM_011525094.2:c.-207+175A= XP_011523396.1:n.-207+175A=
XM_017024914.1:c.-207+449A= XP_016880403.1:n.-207+449A=
XM_017024916.1:c.-506-217A= XP_016880405.1:n.-506-217A=
XM_017024917.1:c.-207+502A= XP_016880406.1:n.-207+502A=
XM_017024918.2:c.-207+175A= XP_016880407.1:n.-207+175A=
XM_017024919.1:c.-667-217A= XP_016880408.1:n.-667-217A=
XR_934513.3:n.649+346A=
XR_934514.3:n.649+346A=
NM_058216.3:c.145+346A= MANE Select NP_478123.1:n.145+346A=
NR_103872.2:n.187+346A=
NM_002876.4:c.145+346A= NP_002867.1:n.145+346A=