Canonical Allele Identifier: CA2267814260
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58693048C= , CM000679.2:g.58693048C= GRCh38
NC_000017.10:g.56770409C= , CM000679.1:g.56770409C= GRCh37
NC_000017.9:g.54125408C= NCBI36
NG_023199.1:g.5447C= , LRG_314:g.5447C=
NG_047169.1:g.4032G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.-207+363C= ENSP00000464056.2:n.-207+363C=
ENST00000697675.1:n.476C=
ENST00000697676.1:n.205+260C=
ENST00000697677.1:n.463C=
ENST00000697678.1:n.47+416C=
ENST00000697679.1:n.456C=
ENST00000697680.1:c.*246C= ENSP00000513392.1:n.*246C=
ENST00000697681.1:c.*246C= ENSP00000513393.1:n.*246C=
ENST00000697683.1:c.*246C= ENSP00000513395.1:n.*246C=
ENST00000697684.1:n.205+260C=
ENST00000697685.1:c.*246C= ENSP00000513396.1:n.*246C=
ENST00000697686.1:c.-207+416C= ENSP00000513397.1:n.-207+416C=
ENST00000697687.1:n.191+260C=
ENST00000697688.1:n.191+260C=
ENST00000697689.1:c.*246C= ENSP00000513398.1:n.*246C=
ENST00000697690.1:c.145+260C= ENSP00000513399.1:n.145+260C=
ENST00000697691.1:c.43-303C= ENSP00000513400.1:n.43-303C=
ENST00000697692.1:c.*157+89C= ENSP00000513401.1:n.*157+89C=
ENST00000697693.1:n.318C=
ENST00000697694.1:c.-277C= ENSP00000513402.1:n.-277C=
ENST00000697695.1:n.122C=
ENST00000337432.9:c.145+260C= MANE Select ENSP00000336701.4:n.145+260C=
ENST00000337432.8:c.145+260C= ENSP00000336701.4:n.145+260C=
ENST00000421782.3:c.145+260C= ENSP00000391450.2:n.145+260C=
ENST00000461271.5:c.-207+363C= ENSP00000464056.1:n.-207+363C=
ENST00000475762.5:c.*246C= ENSP00000432421.1:n.*246C=
ENST00000476741.2:n.187+260C=
ENST00000482007.5:c.145+260C= ENSP00000433332.1:n.145+260C=
ENST00000486827.1:c.*246C= ENSP00000436761.1:n.*246C=
ENST00000487525.5:c.145+260C= ENSP00000431637.1:n.145+260C=
ENST00000487921.5:n.57+416C=
ENST00000583539.5:c.145+260C= ENSP00000463121.1:n.145+260C=
ENST00000584617.5:c.126+260C=
NM_002876.3:c.145+260C= NP_002867.1:n.145+260C=
NM_058216.2:c.145+260C= NP_478123.1:n.145+260C=
NR_103872.1:n.216+260C=
NR_103873.1:n.113+363C=
XM_006722001.2:c.145+260C= XP_006722064.1:n.145+260C=
XM_006722002.2:c.145+260C= XP_006722065.1:n.145+260C=
XM_006722004.2:c.-207+363C= XP_006722067.1:n.-207+363C=
XM_006722005.2:c.-207+416C= XP_006722068.1:n.-207+416C=
XM_011525092.1:c.-506-303C= XP_011523394.1:n.-506-303C=
XM_011525093.1:c.-667-303C= XP_011523395.1:n.-667-303C=
XM_011525094.1:c.-207+89C= XP_011523396.1:n.-207+89C=
XR_934513.1:n.218+260C=
XR_934514.1:n.218+260C=
XM_006722001.4:c.145+260C= XP_006722064.1:n.145+260C=
XM_006722002.4:c.145+260C= XP_006722065.1:n.145+260C=
XM_006722004.3:c.-207+363C= XP_006722067.1:n.-207+363C=
XM_006722005.3:c.-207+416C= XP_006722068.1:n.-207+416C=
XM_011525092.2:c.-506-303C= XP_011523394.1:n.-506-303C=
XM_011525093.2:c.-667-303C= XP_011523395.1:n.-667-303C=
XM_011525094.2:c.-207+89C= XP_011523396.1:n.-207+89C=
XM_017024914.1:c.-207+363C= XP_016880403.1:n.-207+363C=
XM_017024916.1:c.-506-303C= XP_016880405.1:n.-506-303C=
XM_017024917.1:c.-207+416C= XP_016880406.1:n.-207+416C=
XM_017024918.2:c.-207+89C= XP_016880407.1:n.-207+89C=
XM_017024919.1:c.-667-303C= XP_016880408.1:n.-667-303C=
XR_934513.3:n.649+260C=
XR_934514.3:n.649+260C=
NM_058216.3:c.145+260C= MANE Select NP_478123.1:n.145+260C=
NR_103872.2:n.187+260C=
NM_002876.4:c.145+260C= NP_002867.1:n.145+260C=