Canonical Allele Identifier: CA2638988868

Gene: RAD51C

Linked Data

• gnomAD v4: 17-58692806-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692808dup , CM000679.2:g.58692808dup	GRCh38
NC_000017.10:g.56770169dup , CM000679.1:g.56770169dup	GRCh37
NC_000017.9:g.54125168dup	NCBI36
NG_023199.1:g.5207dup , LRG_314:g.5207dup
NG_047169.1:g.4273dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-207+123dup	ENSP00000464056.2:n.-207+123dup
ENST00000697675.1:n.236dup
ENST00000697676.1:n.205+20dup
ENST00000697677.1:n.223dup
ENST00000697678.1:n.47+176dup
ENST00000697679.1:n.216dup
ENST00000697680.1:c.*6dup	ENSP00000513392.1:n.*6dup
ENST00000697681.1:c.*6dup	ENSP00000513393.1:n.*6dup
ENST00000697683.1:c.*6dup	ENSP00000513395.1:n.*6dup
ENST00000697684.1:n.205+20dup
ENST00000697685.1:c.*6dup	ENSP00000513396.1:n.*6dup
ENST00000697686.1:c.-207+176dup	ENSP00000513397.1:n.-207+176dup
ENST00000697687.1:n.191+20dup
ENST00000697688.1:n.191+20dup
ENST00000697689.1:c.*6dup	ENSP00000513398.1:n.*6dup
ENST00000697690.1:c.145+20dup	ENSP00000513399.1:n.145+20dup
ENST00000697691.1:c.42+123dup	ENSP00000513400.1:n.42+123dup
ENST00000697692.1:c.*6dup	ENSP00000513401.1:n.*6dup
ENST00000697693.1:n.78dup
ENST00000337432.9:c.145+20dup MANE Select	ENSP00000336701.4:n.145+20dup
ENST00000337432.8:c.145+20dup	ENSP00000336701.4:n.145+20dup
ENST00000421782.3:c.145+20dup	ENSP00000391450.2:n.145+20dup
ENST00000461271.5:c.-207+123dup	ENSP00000464056.1:n.-207+123dup
ENST00000475762.5:c.*6dup	ENSP00000432421.1:n.*6dup
ENST00000476741.2:n.187+20dup
ENST00000482007.5:c.145+20dup	ENSP00000433332.1:n.145+20dup
ENST00000486827.1:c.*6dup	ENSP00000436761.1:n.*6dup
ENST00000487525.5:c.145+20dup	ENSP00000431637.1:n.145+20dup
ENST00000487921.5:n.57+176dup
ENST00000583539.5:c.145+20dup	ENSP00000463121.1:n.145+20dup
ENST00000584617.5:c.126+20dup
NM_002876.3:c.145+20dup	NP_002867.1:n.145+20dup
NM_058216.2:c.145+20dup	NP_478123.1:n.145+20dup
NR_103872.1:n.216+20dup
NR_103873.1:n.113+123dup
XM_006722001.2:c.145+20dup	XP_006722064.1:n.145+20dup
XM_006722002.2:c.145+20dup	XP_006722065.1:n.145+20dup
XM_006722004.2:c.-207+123dup	XP_006722067.1:n.-207+123dup
XM_006722005.2:c.-207+176dup	XP_006722068.1:n.-207+176dup
XM_011525092.1:c.-507+123dup	XP_011523394.1:n.-507+123dup
XM_011525093.1:c.-668+123dup	XP_011523395.1:n.-668+123dup
XM_011525094.1:c.-358dup	XP_011523396.1:n.-358dup
XR_934513.1:n.218+20dup
XR_934514.1:n.218+20dup
XM_006722001.4:c.145+20dup	XP_006722064.1:n.145+20dup
XM_006722002.4:c.145+20dup	XP_006722065.1:n.145+20dup
XM_006722004.3:c.-207+123dup	XP_006722067.1:n.-207+123dup
XM_006722005.3:c.-207+176dup	XP_006722068.1:n.-207+176dup
XM_011525092.2:c.-507+123dup	XP_011523394.1:n.-507+123dup
XM_011525093.2:c.-668+123dup	XP_011523395.1:n.-668+123dup
XM_011525094.2:c.-358dup	XP_011523396.1:n.-358dup
XM_017024914.1:c.-207+123dup	XP_016880403.1:n.-207+123dup
XM_017024916.1:c.-507+123dup	XP_016880405.1:n.-507+123dup
XM_017024917.1:c.-207+176dup	XP_016880406.1:n.-207+176dup
XM_017024918.2:c.-358dup	XP_016880407.1:n.-358dup
XM_017024919.1:c.-668+123dup	XP_016880408.1:n.-668+123dup
XR_934513.3:n.649+20dup
XR_934514.3:n.649+20dup
NM_058216.3:c.145+20dup MANE Select	NP_478123.1:n.145+20dup
NR_103872.2:n.187+20dup
NM_002876.4:c.145+20dup	NP_002867.1:n.145+20dup