Canonical Allele Identifier: CA913188858

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 629079
• ClinVar RCV Id: RCV002534096
• dbSNP Id: rs1567794083

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703189G>A , CM000679.2:g.58703189G>A	GRCh38
NC_000017.10:g.56780550G>A , CM000679.1:g.56780550G>A	GRCh37
NC_000017.9:g.54135549G>A	NCBI36
NG_023199.1:g.15588G>A , LRG_314:g.15588G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.221-7G>A	ENSP00000464056.2:n.221-7G>A
ENST00000697677.1:n.1653-7G>A
ENST00000697678.1:n.474-7G>A
ENST00000697679.1:n.1646-7G>A
ENST00000697680.1:c.*1436-7G>A	ENSP00000513392.1:n.*1436-7G>A
ENST00000697681.1:c.*1588-7G>A	ENSP00000513393.1:n.*1588-7G>A
ENST00000697683.1:c.*1436-7G>A	ENSP00000513395.1:n.*1436-7G>A
ENST00000697684.1:n.632-7G>A
ENST00000697685.1:c.*1269-7G>A	ENSP00000513396.1:n.*1269-7G>A
ENST00000697686.1:c.221-7G>A	ENSP00000513397.1:n.221-7G>A
ENST00000697687.1:n.451-7G>A
ENST00000697688.1:n.618-7G>A
ENST00000697689.1:c.*1108-7G>A	ENSP00000513398.1:n.*1108-7G>A
ENST00000697690.1:c.572-7G>A	ENSP00000513399.1:n.572-7G>A
ENST00000697691.1:c.*544-7G>A	ENSP00000513400.1:n.*544-7G>A
ENST00000697692.1:c.*584-7G>A	ENSP00000513401.1:n.*584-7G>A
ENST00000697694.1:c.221-7G>A	ENSP00000513402.1:n.221-7G>A
ENST00000697695.1:n.1179-7G>A
ENST00000337432.9:c.572-7G>A MANE Select	ENSP00000336701.4:n.572-7G>A
ENST00000337432.8:c.572-7G>A	ENSP00000336701.4:n.572-7G>A
ENST00000413590.5:c.210-7G>A
ENST00000425173.5:c.368-7G>A	ENSP00000407282.1:n.368-7G>A
ENST00000461271.5:c.221-7G>A	ENSP00000464056.1:n.221-7G>A
ENST00000475762.5:c.*1275-7G>A	ENSP00000432421.1:n.*1275-7G>A
ENST00000482007.5:c.405-7G>A	ENSP00000433332.1:n.405-7G>A
ENST00000487525.5:c.405-7G>A	ENSP00000431637.1:n.405-7G>A
ENST00000487921.5:n.484-7G>A
ENST00000583539.5:c.572-7G>A	ENSP00000463121.1:n.572-7G>A
ENST00000584617.5:c.294-7G>A
NM_058216.2:c.572-7G>A	NP_478123.1:n.572-7G>A
NR_103872.1:n.476-7G>A
XM_006722001.2:c.572-7G>A	XP_006722064.1:n.572-7G>A
XM_006722002.2:c.572-7G>A	XP_006722065.1:n.572-7G>A
XM_006722004.2:c.221-7G>A	XP_006722067.1:n.221-7G>A
XM_006722005.2:c.221-7G>A	XP_006722068.1:n.221-7G>A
XM_011525092.1:c.221-7G>A	XP_011523394.1:n.221-7G>A
XM_011525093.1:c.221-7G>A	XP_011523395.1:n.221-7G>A
XM_011525094.1:c.221-7G>A	XP_011523396.1:n.221-7G>A
XR_934513.1:n.645-7G>A
XR_934514.1:n.645-7G>A
XM_006722001.4:c.572-7G>A	XP_006722064.1:n.572-7G>A
XM_006722002.4:c.572-7G>A	XP_006722065.1:n.572-7G>A
XM_006722004.3:c.221-7G>A	XP_006722067.1:n.221-7G>A
XM_006722005.3:c.221-7G>A	XP_006722068.1:n.221-7G>A
XM_011525092.2:c.221-7G>A	XP_011523394.1:n.221-7G>A
XM_011525093.2:c.221-7G>A	XP_011523395.1:n.221-7G>A
XM_011525094.2:c.221-7G>A	XP_011523396.1:n.221-7G>A
XM_017024914.1:c.221-7G>A	XP_016880403.1:n.221-7G>A
XM_017024915.1:c.221-7G>A	XP_016880404.1:n.221-7G>A
XM_017024916.1:c.221-7G>A	XP_016880405.1:n.221-7G>A
XM_017024917.1:c.221-7G>A	XP_016880406.1:n.221-7G>A
XM_017024918.2:c.221-7G>A	XP_016880407.1:n.221-7G>A
XM_017024919.1:c.221-7G>A	XP_016880408.1:n.221-7G>A
XR_934513.3:n.1076-7G>A
XR_934514.3:n.1076-7G>A
NM_058216.3:c.572-7G>A MANE Select	NP_478123.1:n.572-7G>A
NR_103872.2:n.447-7G>A