Canonical Allele Identifier: CA2267816151
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58696708A= , CM000679.2:g.58696708A= GRCh38
NC_000017.10:g.56774069A= , CM000679.1:g.56774069A= GRCh37
NC_000017.9:g.54129068A= NCBI36
NG_023199.1:g.9107A= , LRG_314:g.9107A=
NG_047169.1:g.372T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.69A= ENSP00000464056.2:p.Val23=
ENST00000697675.1:n.3017A=
ENST00000697676.1:n.480A=
ENST00000697677.1:n.1501A=
ENST00000697678.1:n.322A=
ENST00000697679.1:n.1494A=
ENST00000697680.1:c.*1284A= ENSP00000513392.1:n.*1284A=
ENST00000697681.1:c.*1311A= ENSP00000513393.1:n.*1311A=
ENST00000697683.1:c.*1284A= ENSP00000513395.1:n.*1284A=
ENST00000697684.1:n.480A=
ENST00000697685.1:c.*1268+1519A= ENSP00000513396.1:n.*1268+1519A=
ENST00000697686.1:c.69A= ENSP00000513397.1:p.Val23=
ENST00000697687.1:n.450+1519A=
ENST00000697688.1:n.466A=
ENST00000697689.1:c.*1107+1519A= ENSP00000513398.1:n.*1107+1519A=
ENST00000697690.1:c.420A= ENSP00000513399.1:p.Val140=
ENST00000697691.1:c.*392A= ENSP00000513400.1:n.*392A=
ENST00000697692.1:c.*432A= ENSP00000513401.1:n.*432A=
ENST00000697694.1:c.69A= ENSP00000513402.1:p.Val23=
ENST00000697695.1:n.1027A=
ENST00000337432.9:c.420A= MANE Select ENSP00000336701.4:p.Val140=
ENST00000337432.8:c.420A= ENSP00000336701.4:p.Val140=
ENST00000413590.5:c.58A=
ENST00000425173.5:c.216A= ENSP00000407282.1:p.Val72=
ENST00000461271.5:c.69A= ENSP00000464056.1:p.Val23=
ENST00000475762.5:c.*1123A= ENSP00000432421.1:n.*1123A=
ENST00000482007.5:c.404+1519A= ENSP00000433332.1:n.404+1519A=
ENST00000487525.5:c.404+1519A= ENSP00000431637.1:n.404+1519A=
ENST00000487921.5:n.332A=
ENST00000583539.5:c.420A= ENSP00000463121.1:p.Val140=
ENST00000584617.5:c.142A=
ENST00000622327.4:c.156A= ENSP00000482326.1:p.Val52=
NM_058216.2:c.420A= NP_478123.1:p.Val140=
NR_103872.1:n.475+1519A=
XM_006722001.2:c.420A= XP_006722064.1:p.Val140=
XM_006722002.2:c.420A= XP_006722065.1:p.Val140=
XM_006722004.2:c.69A= XP_006722067.1:p.Val23=
XM_006722005.2:c.69A= XP_006722068.1:p.Val23=
XM_011525092.1:c.69A= XP_011523394.1:p.Val23=
XM_011525093.1:c.69A= XP_011523395.1:p.Val23=
XM_011525094.1:c.69A= XP_011523396.1:p.Val23=
XR_934513.1:n.493A=
XR_934514.1:n.493A=
XM_006722001.4:c.420A= XP_006722064.1:p.Val140=
XM_006722002.4:c.420A= XP_006722065.1:p.Val140=
XM_006722004.3:c.69A= XP_006722067.1:p.Val23=
XM_006722005.3:c.69A= XP_006722068.1:p.Val23=
XM_011525092.2:c.69A= XP_011523394.1:p.Val23=
XM_011525093.2:c.69A= XP_011523395.1:p.Val23=
XM_011525094.2:c.69A= XP_011523396.1:p.Val23=
XM_017024914.1:c.69A= XP_016880403.1:p.Val23=
XM_017024915.1:c.69A= XP_016880404.1:p.Val23=
XM_017024916.1:c.69A= XP_016880405.1:p.Val23=
XM_017024917.1:c.69A= XP_016880406.1:p.Val23=
XM_017024918.2:c.69A= XP_016880407.1:p.Val23=
XM_017024919.1:c.69A= XP_016880408.1:p.Val23=
XR_934513.3:n.924A=
XR_934514.3:n.924A=
NM_058216.3:c.420A= MANE Select NP_478123.1:p.Val140=
NR_103872.2:n.446+1519A=