Canonical Allele Identifier: CA2267819498
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703294T= , CM000679.2:g.58703294T= GRCh38
NC_000017.10:g.56780655T= , CM000679.1:g.56780655T= GRCh37
NC_000017.9:g.54135654T= NCBI36
NG_023199.1:g.15693T= , LRG_314:g.15693T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.319T= ENSP00000464056.2:p.Tyr107=
ENST00000697677.1:n.1751T=
ENST00000697678.1:n.572T=
ENST00000697679.1:n.1744T=
ENST00000697680.1:c.*1534T= ENSP00000513392.1:n.*1534T=
ENST00000697681.1:c.*1686T= ENSP00000513393.1:n.*1686T=
ENST00000697683.1:c.*1534T= ENSP00000513395.1:n.*1534T=
ENST00000697684.1:n.730T=
ENST00000697685.1:c.*1367T= ENSP00000513396.1:n.*1367T=
ENST00000697686.1:c.319T= ENSP00000513397.1:p.Tyr107=
ENST00000697687.1:n.549T=
ENST00000697688.1:n.716T=
ENST00000697689.1:c.*1206T= ENSP00000513398.1:n.*1206T=
ENST00000697690.1:c.670T= ENSP00000513399.1:p.Tyr224=
ENST00000697691.1:c.*642T= ENSP00000513400.1:n.*642T=
ENST00000697692.1:c.*682T= ENSP00000513401.1:n.*682T=
ENST00000697694.1:c.319T= ENSP00000513402.1:p.Tyr107=
ENST00000697695.1:n.1277T=
ENST00000337432.9:c.670T= MANE Select ENSP00000336701.4:p.Tyr224=
ENST00000337432.8:c.670T= ENSP00000336701.4:p.Tyr224=
ENST00000413590.5:c.308T=
ENST00000425173.5:c.466T= ENSP00000407282.1:p.Tyr156=
ENST00000461271.5:c.319T= ENSP00000464056.1:p.Tyr107=
ENST00000475762.5:c.*1373T= ENSP00000432421.1:n.*1373T=
ENST00000482007.5:c.*98T= ENSP00000433332.1:n.*98T=
ENST00000487525.5:c.*98T= ENSP00000431637.1:n.*98T=
ENST00000487921.5:n.582T=
ENST00000583539.5:c.670T= ENSP00000463121.1:p.Tyr224=
ENST00000584617.5:c.392T=
NM_058216.2:c.670T= NP_478123.1:p.Tyr224=
NR_103872.1:n.574T=
XM_006722001.2:c.670T= XP_006722064.1:p.Tyr224=
XM_006722002.2:c.670T= XP_006722065.1:p.Tyr224=
XM_006722004.2:c.319T= XP_006722067.1:p.Tyr107=
XM_006722005.2:c.319T= XP_006722068.1:p.Tyr107=
XM_011525092.1:c.319T= XP_011523394.1:p.Tyr107=
XM_011525093.1:c.319T= XP_011523395.1:p.Tyr107=
XM_011525094.1:c.319T= XP_011523396.1:p.Tyr107=
XR_934513.1:n.743T=
XR_934514.1:n.743T=
XM_006722001.4:c.670T= XP_006722064.1:p.Tyr224=
XM_006722002.4:c.670T= XP_006722065.1:p.Tyr224=
XM_006722004.3:c.319T= XP_006722067.1:p.Tyr107=
XM_006722005.3:c.319T= XP_006722068.1:p.Tyr107=
XM_011525092.2:c.319T= XP_011523394.1:p.Tyr107=
XM_011525093.2:c.319T= XP_011523395.1:p.Tyr107=
XM_011525094.2:c.319T= XP_011523396.1:p.Tyr107=
XM_017024914.1:c.319T= XP_016880403.1:p.Tyr107=
XM_017024915.1:c.319T= XP_016880404.1:p.Tyr107=
XM_017024916.1:c.319T= XP_016880405.1:p.Tyr107=
XM_017024917.1:c.319T= XP_016880406.1:p.Tyr107=
XM_017024918.2:c.319T= XP_016880407.1:p.Tyr107=
XM_017024919.1:c.319T= XP_016880408.1:p.Tyr107=
XR_934513.3:n.1174T=
XR_934514.3:n.1174T=
NM_058216.3:c.670T= MANE Select NP_478123.1:p.Tyr224=
NR_103872.2:n.545T=