Canonical Allele Identifier: CA2267815232
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58694983A= , CM000679.2:g.58694983A= GRCh38
NC_000017.10:g.56772344A= , CM000679.1:g.56772344A= GRCh37
NC_000017.9:g.54127343A= NCBI36
NG_023199.1:g.7382A= , LRG_314:g.7382A=
NG_047169.1:g.2097T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.-154A= ENSP00000464056.2:n.-154A=
ENST00000697675.1:n.1292A=
ENST00000697676.1:n.258A=
ENST00000697677.1:n.1279A=
ENST00000697678.1:n.100A=
ENST00000697679.1:n.1272A=
ENST00000697680.1:c.*1062A= ENSP00000513392.1:n.*1062A=
ENST00000697681.1:c.*1062A= ENSP00000513393.1:n.*1062A=
ENST00000697683.1:c.*1062A= ENSP00000513395.1:n.*1062A=
ENST00000697684.1:n.258A=
ENST00000697685.1:c.*1062A= ENSP00000513396.1:n.*1062A=
ENST00000697686.1:c.-154A= ENSP00000513397.1:n.-154A=
ENST00000697687.1:n.244A=
ENST00000697688.1:n.244A=
ENST00000697689.1:c.*901A= ENSP00000513398.1:n.*901A=
ENST00000697690.1:c.198A= ENSP00000513399.1:p.Arg66=
ENST00000697691.1:c.*170A= ENSP00000513400.1:n.*170A=
ENST00000697692.1:c.*210A= ENSP00000513401.1:n.*210A=
ENST00000697693.1:n.973A=
ENST00000697694.1:c.-154A= ENSP00000513402.1:n.-154A=
ENST00000697695.1:n.805A=
ENST00000337432.9:c.198A= MANE Select ENSP00000336701.4:p.Arg66=
ENST00000337432.8:c.198A= ENSP00000336701.4:p.Arg66=
ENST00000421782.3:c.198A= ENSP00000391450.2:p.Arg66=
ENST00000461271.5:c.-154A= ENSP00000464056.1:n.-154A=
ENST00000475762.5:c.*901A= ENSP00000432421.1:n.*901A=
ENST00000482007.5:c.198A= ENSP00000433332.1:p.Arg66=
ENST00000486827.1:c.*1062A= ENSP00000436761.1:n.*1062A=
ENST00000487525.5:c.198A= ENSP00000431637.1:p.Arg66=
ENST00000487921.5:n.110A=
ENST00000583539.5:c.198A= ENSP00000463121.1:p.Arg66=
ENST00000584617.5:c.127-1710A=
NM_002876.3:c.198A= NP_002867.1:p.Arg66=
NM_058216.2:c.198A= NP_478123.1:p.Arg66=
NR_103872.1:n.269A=
NR_103873.1:n.166A=
XM_006722001.2:c.198A= XP_006722064.1:p.Arg66=
XM_006722002.2:c.198A= XP_006722065.1:p.Arg66=
XM_006722004.2:c.-154A= XP_006722067.1:n.-154A=
XM_006722005.2:c.-154A= XP_006722068.1:n.-154A=
XM_011525092.1:c.-154A= XP_011523394.1:n.-154A=
XM_011525093.1:c.-154A= XP_011523395.1:n.-154A=
XM_011525094.1:c.-154A= XP_011523396.1:n.-154A=
XR_934513.1:n.271A=
XR_934514.1:n.271A=
XM_006722001.4:c.198A= XP_006722064.1:p.Arg66=
XM_006722002.4:c.198A= XP_006722065.1:p.Arg66=
XM_006722004.3:c.-154A= XP_006722067.1:n.-154A=
XM_006722005.3:c.-154A= XP_006722068.1:n.-154A=
XM_011525092.2:c.-154A= XP_011523394.1:n.-154A=
XM_011525093.2:c.-154A= XP_011523395.1:n.-154A=
XM_011525094.2:c.-154A= XP_011523396.1:n.-154A=
XM_017024914.1:c.-154A= XP_016880403.1:n.-154A=
XM_017024915.1:c.-154A= XP_016880404.1:n.-154A=
XM_017024916.1:c.-154A= XP_016880405.1:n.-154A=
XM_017024917.1:c.-154A= XP_016880406.1:n.-154A=
XM_017024918.2:c.-154A= XP_016880407.1:n.-154A=
XM_017024919.1:c.-154A= XP_016880408.1:n.-154A=
XR_934513.3:n.702A=
XR_934514.3:n.702A=
NM_058216.3:c.198A= MANE Select NP_478123.1:p.Arg66=
NR_103872.2:n.240A=
NM_002876.4:c.198A= NP_002867.1:p.Arg66=