Canonical Allele Identifier: CA10580751

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 230728
• ClinVar RCV Id: RCV000219629
• dbSNP Id: rs876658730
• gnomAD v3: 17-58709907-C-G
• gnomAD v4: 17-58709907-C-G
• MyVariant Identifiers: chr17:g.56787268C>G (hg19) ; chr17:g.58709907C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58709907C>G , CM000679.2:g.58709907C>G	GRCh38
NC_000017.10:g.56787268C>G , CM000679.1:g.56787268C>G	GRCh37
NC_000017.9:g.54142267C>G	NCBI36
NG_023199.1:g.22306C>G , LRG_314:g.22306C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.403C>G	ENSP00000464056.2:p.Leu135Val
ENST00000697678.1:n.656C>G
ENST00000697679.1:n.1828C>G
ENST00000697680.1:c.*1618C>G	ENSP00000513392.1:n.*1618C>G
ENST00000697681.1:c.*1915C>G	ENSP00000513393.1:n.*1915C>G
ENST00000697683.1:c.*1618C>G	ENSP00000513395.1:n.*1618C>G
ENST00000697684.1:n.814C>G
ENST00000697685.1:c.*1451C>G	ENSP00000513396.1:n.*1451C>G
ENST00000697686.1:c.403C>G	ENSP00000513397.1:p.Leu135Val
ENST00000697687.1:n.633C>G
ENST00000697688.1:n.800C>G
ENST00000697689.1:c.*1290C>G	ENSP00000513398.1:n.*1290C>G
ENST00000697690.1:c.754C>G	ENSP00000513399.1:p.Leu252Val
ENST00000697691.1:c.*726C>G	ENSP00000513400.1:n.*726C>G
ENST00000697692.1:c.*766C>G	ENSP00000513401.1:n.*766C>G
ENST00000697694.1:c.403C>G	ENSP00000513402.1:p.Leu135Val
ENST00000697695.1:n.1361C>G
ENST00000337432.9:c.754C>G MANE Select	ENSP00000336701.4:p.Leu252Val
ENST00000337432.8:c.754C>G	ENSP00000336701.4:p.Leu252Val
ENST00000413590.5:c.392C>G
ENST00000461271.5:c.403C>G	ENSP00000464056.1:p.Leu135Val
ENST00000475762.5:c.*1457C>G	ENSP00000432421.1:n.*1457C>G
ENST00000482007.5:c.*182C>G	ENSP00000433332.1:n.*182C>G
ENST00000487525.5:c.*327C>G	ENSP00000431637.1:n.*327C>G
ENST00000578151.1:n.89C>G
ENST00000581221.5:n.269C>G
ENST00000583539.5:c.754C>G	ENSP00000463121.1:p.Leu252Val
ENST00000584617.5:c.476C>G
ENST00000584804.1:c.49C>G	ENSP00000463658.1:p.Leu17Val
NM_058216.2:c.754C>G	NP_478123.1:p.Leu252Val
NR_103872.1:n.658C>G
XM_006722001.2:c.754C>G	XP_006722064.1:p.Leu252Val
XM_006722002.2:c.754C>G	XP_006722065.1:p.Leu252Val
XM_006722004.2:c.403C>G	XP_006722067.1:p.Leu135Val
XM_006722005.2:c.403C>G	XP_006722068.1:p.Leu135Val
XM_011525092.1:c.403C>G	XP_011523394.1:p.Leu135Val
XM_011525093.1:c.403C>G	XP_011523395.1:p.Leu135Val
XM_011525094.1:c.403C>G	XP_011523396.1:p.Leu135Val
XR_934513.1:n.972C>G
XR_934514.1:n.972C>G
XM_006722001.4:c.754C>G	XP_006722064.1:p.Leu252Val
XM_006722002.4:c.754C>G	XP_006722065.1:p.Leu252Val
XM_006722004.3:c.403C>G	XP_006722067.1:p.Leu135Val
XM_006722005.3:c.403C>G	XP_006722068.1:p.Leu135Val
XM_011525092.2:c.403C>G	XP_011523394.1:p.Leu135Val
XM_011525093.2:c.403C>G	XP_011523395.1:p.Leu135Val
XM_011525094.2:c.403C>G	XP_011523396.1:p.Leu135Val
XM_017024914.1:c.403C>G	XP_016880403.1:p.Leu135Val
XM_017024915.1:c.403C>G	XP_016880404.1:p.Leu135Val
XM_017024916.1:c.403C>G	XP_016880405.1:p.Leu135Val
XM_017024917.1:c.403C>G	XP_016880406.1:p.Leu135Val
XM_017024918.2:c.403C>G	XP_016880407.1:p.Leu135Val
XM_017024919.1:c.403C>G	XP_016880408.1:p.Leu135Val
XR_934513.3:n.1403C>G
XR_934514.3:n.1403C>G
NM_058216.3:c.754C>G MANE Select	NP_478123.1:p.Leu252Val
NR_103872.2:n.629C>G