Canonical Allele Identifier: CA288627

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 128208
• ClinVar RCV Id: RCV000116177 ; RCV000773140 ; RCV002055276 ; RCV002465522 ; RCV003975003
• dbSNP Id: rs587780258
• ExAC: 17:56780542 GT / G
• gnomAD v2: 17-56780542-GT-G
• gnomAD v3: 17-58703181-GT-G
• gnomAD v4: 17-58703181-GT-G
• MyVariant Identifiers: chr17:g.56780546del (hg19) ; chr17:g.56780543del (hg19) ; chr17:g.58703185del (hg38) ; chr17:g.58703183del (hg38) ; chr17:g.58703182del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703185del , CM000679.2:g.58703185del	GRCh38
NC_000017.10:g.56780546del , CM000679.1:g.56780546del	GRCh37
NC_000017.9:g.54135545del	NCBI36
NG_023199.1:g.15584del , LRG_314:g.15584del

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.221-11del	ENSP00000464056.2:n.221-11del
ENST00000697677.1:n.1653-11del
ENST00000697678.1:n.474-11del
ENST00000697679.1:n.1646-11del
ENST00000697680.1:c.*1436-11del	ENSP00000513392.1:n.*1436-11del
ENST00000697681.1:c.*1588-11del	ENSP00000513393.1:n.*1588-11del
ENST00000697683.1:c.*1436-11del	ENSP00000513395.1:n.*1436-11del
ENST00000697684.1:n.632-11del
ENST00000697685.1:c.*1269-11del	ENSP00000513396.1:n.*1269-11del
ENST00000697686.1:c.221-11del	ENSP00000513397.1:n.221-11del
ENST00000697687.1:n.451-11del
ENST00000697688.1:n.618-11del
ENST00000697689.1:c.*1108-11del	ENSP00000513398.1:n.*1108-11del
ENST00000697690.1:c.572-11del	ENSP00000513399.1:n.572-11del
ENST00000697691.1:c.*544-11del	ENSP00000513400.1:n.*544-11del
ENST00000697692.1:c.*584-11del	ENSP00000513401.1:n.*584-11del
ENST00000697694.1:c.221-11del	ENSP00000513402.1:n.221-11del
ENST00000697695.1:n.1179-11del
ENST00000337432.9:c.572-11del MANE Select	ENSP00000336701.4:n.572-11del
ENST00000337432.8:c.572-11del	ENSP00000336701.4:n.572-11del
ENST00000413590.5:c.210-11del
ENST00000425173.5:c.368-11del	ENSP00000407282.1:n.368-11del
ENST00000461271.5:c.221-11del	ENSP00000464056.1:n.221-11del
ENST00000475762.5:c.*1275-11del	ENSP00000432421.1:n.*1275-11del
ENST00000482007.5:c.405-11del	ENSP00000433332.1:n.405-11del
ENST00000487525.5:c.405-11del	ENSP00000431637.1:n.405-11del
ENST00000487921.5:n.484-11del
ENST00000583539.5:c.572-11del	ENSP00000463121.1:n.572-11del
ENST00000584617.5:c.294-11del
NM_058216.2:c.572-11del	NP_478123.1:n.572-11del
NR_103872.1:n.476-11del
XM_006722001.2:c.572-11del	XP_006722064.1:n.572-11del
XM_006722002.2:c.572-11del	XP_006722065.1:n.572-11del
XM_006722004.2:c.221-11del	XP_006722067.1:n.221-11del
XM_006722005.2:c.221-11del	XP_006722068.1:n.221-11del
XM_011525092.1:c.221-11del	XP_011523394.1:n.221-11del
XM_011525093.1:c.221-11del	XP_011523395.1:n.221-11del
XM_011525094.1:c.221-11del	XP_011523396.1:n.221-11del
XR_934513.1:n.645-11del
XR_934514.1:n.645-11del
XM_006722001.4:c.572-11del	XP_006722064.1:n.572-11del
XM_006722002.4:c.572-11del	XP_006722065.1:n.572-11del
XM_006722004.3:c.221-11del	XP_006722067.1:n.221-11del
XM_006722005.3:c.221-11del	XP_006722068.1:n.221-11del
XM_011525092.2:c.221-11del	XP_011523394.1:n.221-11del
XM_011525093.2:c.221-11del	XP_011523395.1:n.221-11del
XM_011525094.2:c.221-11del	XP_011523396.1:n.221-11del
XM_017024914.1:c.221-11del	XP_016880403.1:n.221-11del
XM_017024915.1:c.221-11del	XP_016880404.1:n.221-11del
XM_017024916.1:c.221-11del	XP_016880405.1:n.221-11del
XM_017024917.1:c.221-11del	XP_016880406.1:n.221-11del
XM_017024918.2:c.221-11del	XP_016880407.1:n.221-11del
XM_017024919.1:c.221-11del	XP_016880408.1:n.221-11del
XR_934513.3:n.1076-11del
XR_934514.3:n.1076-11del
NM_058216.3:c.572-11del MANE Select	NP_478123.1:n.572-11del
NR_103872.2:n.447-11del