Canonical Allele Identifier: CA2267819514
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703322A= , CM000679.2:g.58703322A= GRCh38
NC_000017.10:g.56780683A= , CM000679.1:g.56780683A= GRCh37
NC_000017.9:g.54135682A= NCBI36
NG_023199.1:g.15721A= , LRG_314:g.15721A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.347A= ENSP00000464056.2:p.His116=
ENST00000697677.1:n.1779A=
ENST00000697678.1:n.600A=
ENST00000697679.1:n.1772A=
ENST00000697680.1:c.*1562A= ENSP00000513392.1:n.*1562A=
ENST00000697681.1:c.*1714A= ENSP00000513393.1:n.*1714A=
ENST00000697683.1:c.*1562A= ENSP00000513395.1:n.*1562A=
ENST00000697684.1:n.758A=
ENST00000697685.1:c.*1395A= ENSP00000513396.1:n.*1395A=
ENST00000697686.1:c.347A= ENSP00000513397.1:p.His116=
ENST00000697687.1:n.577A=
ENST00000697688.1:n.744A=
ENST00000697689.1:c.*1234A= ENSP00000513398.1:n.*1234A=
ENST00000697690.1:c.698A= ENSP00000513399.1:p.His233=
ENST00000697691.1:c.*670A= ENSP00000513400.1:n.*670A=
ENST00000697692.1:c.*710A= ENSP00000513401.1:n.*710A=
ENST00000697694.1:c.347A= ENSP00000513402.1:p.His116=
ENST00000697695.1:n.1305A=
ENST00000337432.9:c.698A= MANE Select ENSP00000336701.4:p.His233=
ENST00000337432.8:c.698A= ENSP00000336701.4:p.His233=
ENST00000413590.5:c.336A=
ENST00000425173.5:c.494A= ENSP00000407282.1:p.His165=
ENST00000461271.5:c.347A= ENSP00000464056.1:p.His116=
ENST00000475762.5:c.*1401A= ENSP00000432421.1:n.*1401A=
ENST00000482007.5:c.*126A= ENSP00000433332.1:n.*126A=
ENST00000487525.5:c.*126A= ENSP00000431637.1:n.*126A=
ENST00000487921.5:n.610A=
ENST00000583539.5:c.698A= ENSP00000463121.1:p.His233=
ENST00000584617.5:c.420A=
NM_058216.2:c.698A= NP_478123.1:p.His233=
NR_103872.1:n.602A=
XM_006722001.2:c.698A= XP_006722064.1:p.His233=
XM_006722002.2:c.698A= XP_006722065.1:p.His233=
XM_006722004.2:c.347A= XP_006722067.1:p.His116=
XM_006722005.2:c.347A= XP_006722068.1:p.His116=
XM_011525092.1:c.347A= XP_011523394.1:p.His116=
XM_011525093.1:c.347A= XP_011523395.1:p.His116=
XM_011525094.1:c.347A= XP_011523396.1:p.His116=
XR_934513.1:n.771A=
XR_934514.1:n.771A=
XM_006722001.4:c.698A= XP_006722064.1:p.His233=
XM_006722002.4:c.698A= XP_006722065.1:p.His233=
XM_006722004.3:c.347A= XP_006722067.1:p.His116=
XM_006722005.3:c.347A= XP_006722068.1:p.His116=
XM_011525092.2:c.347A= XP_011523394.1:p.His116=
XM_011525093.2:c.347A= XP_011523395.1:p.His116=
XM_011525094.2:c.347A= XP_011523396.1:p.His116=
XM_017024914.1:c.347A= XP_016880403.1:p.His116=
XM_017024915.1:c.347A= XP_016880404.1:p.His116=
XM_017024916.1:c.347A= XP_016880405.1:p.His116=
XM_017024917.1:c.347A= XP_016880406.1:p.His116=
XM_017024918.2:c.347A= XP_016880407.1:p.His116=
XM_017024919.1:c.347A= XP_016880408.1:p.His116=
XR_934513.3:n.1202A=
XR_934514.3:n.1202A=
NM_058216.3:c.698A= MANE Select NP_478123.1:p.His233=
NR_103872.2:n.573A=