Canonical Allele Identifier: CA400353171

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 478612
• ClinVar RCV Id: RCV000536020
• dbSNP Id: rs863224806
• MyVariant Identifiers: chr17:g.56787232A>G (hg19) ; chr17:g.58709871A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58709871A>G , CM000679.2:g.58709871A>G	GRCh38
NC_000017.10:g.56787232A>G , CM000679.1:g.56787232A>G	GRCh37
NC_000017.9:g.54142231A>G	NCBI36
NG_023199.1:g.22270A>G , LRG_314:g.22270A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.367A>G	ENSP00000464056.2:p.Ile123Val
ENST00000697678.1:n.620A>G
ENST00000697679.1:n.1792A>G
ENST00000697680.1:c.*1582A>G	ENSP00000513392.1:n.*1582A>G
ENST00000697681.1:c.*1879A>G	ENSP00000513393.1:n.*1879A>G
ENST00000697683.1:c.*1582A>G	ENSP00000513395.1:n.*1582A>G
ENST00000697684.1:n.778A>G
ENST00000697685.1:c.*1415A>G	ENSP00000513396.1:n.*1415A>G
ENST00000697686.1:c.367A>G	ENSP00000513397.1:p.Ile123Val
ENST00000697687.1:n.597A>G
ENST00000697688.1:n.764A>G
ENST00000697689.1:c.*1254A>G	ENSP00000513398.1:n.*1254A>G
ENST00000697690.1:c.718A>G	ENSP00000513399.1:p.Ile240Val
ENST00000697691.1:c.*690A>G	ENSP00000513400.1:n.*690A>G
ENST00000697692.1:c.*730A>G	ENSP00000513401.1:n.*730A>G
ENST00000697694.1:c.367A>G	ENSP00000513402.1:p.Ile123Val
ENST00000697695.1:n.1325A>G
ENST00000337432.9:c.718A>G MANE Select	ENSP00000336701.4:p.Ile240Val
ENST00000337432.8:c.718A>G	ENSP00000336701.4:p.Ile240Val
ENST00000413590.5:c.356A>G
ENST00000425173.5:c.634A>G	ENSP00000407282.1:p.Ile212Val
ENST00000461271.5:c.367A>G	ENSP00000464056.1:p.Ile123Val
ENST00000475762.5:c.*1421A>G	ENSP00000432421.1:n.*1421A>G
ENST00000482007.5:c.*146A>G	ENSP00000433332.1:n.*146A>G
ENST00000487525.5:c.*291A>G	ENSP00000431637.1:n.*291A>G
ENST00000578151.1:n.53A>G
ENST00000581221.5:n.233A>G
ENST00000583539.5:c.718A>G	ENSP00000463121.1:p.Ile240Val
ENST00000584617.5:c.440A>G
ENST00000584804.1:c.13A>G	ENSP00000463658.1:p.Ile5Val
NM_058216.2:c.718A>G	NP_478123.1:p.Ile240Val
NR_103872.1:n.622A>G
XM_006722001.2:c.718A>G	XP_006722064.1:p.Ile240Val
XM_006722002.2:c.718A>G	XP_006722065.1:p.Ile240Val
XM_006722004.2:c.367A>G	XP_006722067.1:p.Ile123Val
XM_006722005.2:c.367A>G	XP_006722068.1:p.Ile123Val
XM_011525092.1:c.367A>G	XP_011523394.1:p.Ile123Val
XM_011525093.1:c.367A>G	XP_011523395.1:p.Ile123Val
XM_011525094.1:c.367A>G	XP_011523396.1:p.Ile123Val
XR_934513.1:n.936A>G
XR_934514.1:n.936A>G
XM_006722001.4:c.718A>G	XP_006722064.1:p.Ile240Val
XM_006722002.4:c.718A>G	XP_006722065.1:p.Ile240Val
XM_006722004.3:c.367A>G	XP_006722067.1:p.Ile123Val
XM_006722005.3:c.367A>G	XP_006722068.1:p.Ile123Val
XM_011525092.2:c.367A>G	XP_011523394.1:p.Ile123Val
XM_011525093.2:c.367A>G	XP_011523395.1:p.Ile123Val
XM_011525094.2:c.367A>G	XP_011523396.1:p.Ile123Val
XM_017024914.1:c.367A>G	XP_016880403.1:p.Ile123Val
XM_017024915.1:c.367A>G	XP_016880404.1:p.Ile123Val
XM_017024916.1:c.367A>G	XP_016880405.1:p.Ile123Val
XM_017024917.1:c.367A>G	XP_016880406.1:p.Ile123Val
XM_017024918.2:c.367A>G	XP_016880407.1:p.Ile123Val
XM_017024919.1:c.367A>G	XP_016880408.1:p.Ile123Val
XR_934513.3:n.1367A>G
XR_934514.3:n.1367A>G
NM_058216.3:c.718A>G MANE Select	NP_478123.1:p.Ile240Val
NR_103872.2:n.593A>G