Canonical Allele Identifier: CA2267819451
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703217A= , CM000679.2:g.58703217A= GRCh38
NC_000017.10:g.56780578A= , CM000679.1:g.56780578A= GRCh37
NC_000017.9:g.54135577A= NCBI36
NG_023199.1:g.15616A= , LRG_314:g.15616A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.242A= ENSP00000464056.2:p.Asp81=
ENST00000697677.1:n.1674A=
ENST00000697678.1:n.495A=
ENST00000697679.1:n.1667A=
ENST00000697680.1:c.*1457A= ENSP00000513392.1:n.*1457A=
ENST00000697681.1:c.*1609A= ENSP00000513393.1:n.*1609A=
ENST00000697683.1:c.*1457A= ENSP00000513395.1:n.*1457A=
ENST00000697684.1:n.653A=
ENST00000697685.1:c.*1290A= ENSP00000513396.1:n.*1290A=
ENST00000697686.1:c.242A= ENSP00000513397.1:p.Asp81=
ENST00000697687.1:n.472A=
ENST00000697688.1:n.639A=
ENST00000697689.1:c.*1129A= ENSP00000513398.1:n.*1129A=
ENST00000697690.1:c.593A= ENSP00000513399.1:p.Asp198=
ENST00000697691.1:c.*565A= ENSP00000513400.1:n.*565A=
ENST00000697692.1:c.*605A= ENSP00000513401.1:n.*605A=
ENST00000697694.1:c.242A= ENSP00000513402.1:p.Asp81=
ENST00000697695.1:n.1200A=
ENST00000337432.9:c.593A= MANE Select ENSP00000336701.4:p.Asp198=
ENST00000337432.8:c.593A= ENSP00000336701.4:p.Asp198=
ENST00000413590.5:c.231A=
ENST00000425173.5:c.389A= ENSP00000407282.1:p.Asp130=
ENST00000461271.5:c.242A= ENSP00000464056.1:p.Asp81=
ENST00000475762.5:c.*1296A= ENSP00000432421.1:n.*1296A=
ENST00000482007.5:c.*21A= ENSP00000433332.1:n.*21A=
ENST00000487525.5:c.*21A= ENSP00000431637.1:n.*21A=
ENST00000487921.5:n.505A=
ENST00000583539.5:c.593A= ENSP00000463121.1:p.Asp198=
ENST00000584617.5:c.315A=
NM_058216.2:c.593A= NP_478123.1:p.Asp198=
NR_103872.1:n.497A=
XM_006722001.2:c.593A= XP_006722064.1:p.Asp198=
XM_006722002.2:c.593A= XP_006722065.1:p.Asp198=
XM_006722004.2:c.242A= XP_006722067.1:p.Asp81=
XM_006722005.2:c.242A= XP_006722068.1:p.Asp81=
XM_011525092.1:c.242A= XP_011523394.1:p.Asp81=
XM_011525093.1:c.242A= XP_011523395.1:p.Asp81=
XM_011525094.1:c.242A= XP_011523396.1:p.Asp81=
XR_934513.1:n.666A=
XR_934514.1:n.666A=
XM_006722001.4:c.593A= XP_006722064.1:p.Asp198=
XM_006722002.4:c.593A= XP_006722065.1:p.Asp198=
XM_006722004.3:c.242A= XP_006722067.1:p.Asp81=
XM_006722005.3:c.242A= XP_006722068.1:p.Asp81=
XM_011525092.2:c.242A= XP_011523394.1:p.Asp81=
XM_011525093.2:c.242A= XP_011523395.1:p.Asp81=
XM_011525094.2:c.242A= XP_011523396.1:p.Asp81=
XM_017024914.1:c.242A= XP_016880403.1:p.Asp81=
XM_017024915.1:c.242A= XP_016880404.1:p.Asp81=
XM_017024916.1:c.242A= XP_016880405.1:p.Asp81=
XM_017024917.1:c.242A= XP_016880406.1:p.Asp81=
XM_017024918.2:c.242A= XP_016880407.1:p.Asp81=
XM_017024919.1:c.242A= XP_016880408.1:p.Asp81=
XR_934513.3:n.1097A=
XR_934514.3:n.1097A=
NM_058216.3:c.593A= MANE Select NP_478123.1:p.Asp198=
NR_103872.2:n.468A=