Canonical Allele Identifier: CA2267814315

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58693137T= , CM000679.2:g.58693137T=	GRCh38
NC_000017.10:g.56770498T= , CM000679.1:g.56770498T=	GRCh37
NC_000017.9:g.54125497T=	NCBI36
NG_023199.1:g.5536T= , LRG_314:g.5536T=
NG_047169.1:g.3943A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-207+452T=	ENSP00000464056.2:n.-207+452T=
ENST00000697675.1:n.565T=
ENST00000697676.1:n.205+349T=
ENST00000697677.1:n.552T=
ENST00000697678.1:n.47+505T=
ENST00000697679.1:n.545T=
ENST00000697680.1:c.*335T=	ENSP00000513392.1:n.*335T=
ENST00000697681.1:c.*335T=	ENSP00000513393.1:n.*335T=
ENST00000697683.1:c.*335T=	ENSP00000513395.1:n.*335T=
ENST00000697684.1:n.205+349T=
ENST00000697685.1:c.*335T=	ENSP00000513396.1:n.*335T=
ENST00000697686.1:c.-207+505T=	ENSP00000513397.1:n.-207+505T=
ENST00000697687.1:n.191+349T=
ENST00000697688.1:n.191+349T=
ENST00000697689.1:c.*335T=	ENSP00000513398.1:n.*335T=
ENST00000697690.1:c.145+349T=	ENSP00000513399.1:n.145+349T=
ENST00000697691.1:c.43-214T=	ENSP00000513400.1:n.43-214T=
ENST00000697692.1:c.*157+178T=	ENSP00000513401.1:n.*157+178T=
ENST00000697693.1:n.407T=
ENST00000697694.1:c.-207+19T=	ENSP00000513402.1:n.-207+19T=
ENST00000697695.1:n.211T=
ENST00000337432.9:c.145+349T= MANE Select	ENSP00000336701.4:n.145+349T=
ENST00000337432.8:c.145+349T=	ENSP00000336701.4:n.145+349T=
ENST00000421782.3:c.145+349T=	ENSP00000391450.2:n.145+349T=
ENST00000461271.5:c.-207+452T=	ENSP00000464056.1:n.-207+452T=
ENST00000475762.5:c.*335T=	ENSP00000432421.1:n.*335T=
ENST00000476741.2:n.188-214T=
ENST00000482007.5:c.145+349T=	ENSP00000433332.1:n.145+349T=
ENST00000486827.1:c.*335T=	ENSP00000436761.1:n.*335T=
ENST00000487525.5:c.145+349T=	ENSP00000431637.1:n.145+349T=
ENST00000487921.5:n.57+505T=
ENST00000583539.5:c.145+349T=	ENSP00000463121.1:n.145+349T=
ENST00000584617.5:c.126+349T=
NM_002876.3:c.145+349T=	NP_002867.1:n.145+349T=
NM_058216.2:c.145+349T=	NP_478123.1:n.145+349T=
NR_103872.1:n.216+349T=
NR_103873.1:n.113+452T=
XM_006722001.2:c.145+349T=	XP_006722064.1:n.145+349T=
XM_006722002.2:c.145+349T=	XP_006722065.1:n.145+349T=
XM_006722004.2:c.-207+452T=	XP_006722067.1:n.-207+452T=
XM_006722005.2:c.-207+505T=	XP_006722068.1:n.-207+505T=
XM_011525092.1:c.-506-214T=	XP_011523394.1:n.-506-214T=
XM_011525093.1:c.-667-214T=	XP_011523395.1:n.-667-214T=
XM_011525094.1:c.-207+178T=	XP_011523396.1:n.-207+178T=
XR_934513.1:n.218+349T=
XR_934514.1:n.218+349T=
XM_006722001.4:c.145+349T=	XP_006722064.1:n.145+349T=
XM_006722002.4:c.145+349T=	XP_006722065.1:n.145+349T=
XM_006722004.3:c.-207+452T=	XP_006722067.1:n.-207+452T=
XM_006722005.3:c.-207+505T=	XP_006722068.1:n.-207+505T=
XM_011525092.2:c.-506-214T=	XP_011523394.1:n.-506-214T=
XM_011525093.2:c.-667-214T=	XP_011523395.1:n.-667-214T=
XM_011525094.2:c.-207+178T=	XP_011523396.1:n.-207+178T=
XM_017024914.1:c.-207+452T=	XP_016880403.1:n.-207+452T=
XM_017024916.1:c.-506-214T=	XP_016880405.1:n.-506-214T=
XM_017024917.1:c.-207+505T=	XP_016880406.1:n.-207+505T=
XM_017024918.2:c.-207+178T=	XP_016880407.1:n.-207+178T=
XM_017024919.1:c.-667-214T=	XP_016880408.1:n.-667-214T=
XR_934513.3:n.649+349T=
XR_934514.3:n.649+349T=
NM_058216.3:c.145+349T= MANE Select	NP_478123.1:n.145+349T=
NR_103872.2:n.187+349T=
NM_002876.4:c.145+349T=	NP_002867.1:n.145+349T=