Canonical Allele Identifier: CA349183

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 219853
• ClinVar RCV Id: RCV000205015 ; RCV000486898 ; RCV000570805 ; RCV000663210 ; RCV003316135
• dbSNP Id: rs864622278
• gnomAD v4: 17-58696808-A-G
• MyVariant Identifiers: chr17:g.56774169A>G (hg19) ; chr17:g.58696808A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58696808A>G , CM000679.2:g.58696808A>G	GRCh38
NC_000017.10:g.56774169A>G , CM000679.1:g.56774169A>G	GRCh37
NC_000017.9:g.54129168A>G	NCBI36
NG_023199.1:g.9207A>G , LRG_314:g.9207A>G
NG_047169.1:g.272T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.169A>G	ENSP00000464056.2:p.Thr57Ala
ENST00000697675.1:n.3117A>G
ENST00000697676.1:n.580A>G
ENST00000697677.1:n.1601A>G
ENST00000697678.1:n.422A>G
ENST00000697679.1:n.1594A>G
ENST00000697680.1:c.*1384A>G	ENSP00000513392.1:n.*1384A>G
ENST00000697681.1:c.*1411A>G	ENSP00000513393.1:n.*1411A>G
ENST00000697683.1:c.*1384A>G	ENSP00000513395.1:n.*1384A>G
ENST00000697684.1:n.580A>G
ENST00000697685.1:c.*1268+1619A>G	ENSP00000513396.1:n.*1268+1619A>G
ENST00000697686.1:c.169A>G	ENSP00000513397.1:p.Thr57Ala
ENST00000697687.1:n.450+1619A>G
ENST00000697688.1:n.566A>G
ENST00000697689.1:c.*1107+1619A>G	ENSP00000513398.1:n.*1107+1619A>G
ENST00000697690.1:c.520A>G	ENSP00000513399.1:p.Thr174Ala
ENST00000697691.1:c.*492A>G	ENSP00000513400.1:n.*492A>G
ENST00000697692.1:c.*532A>G	ENSP00000513401.1:n.*532A>G
ENST00000697694.1:c.169A>G	ENSP00000513402.1:p.Thr57Ala
ENST00000697695.1:n.1127A>G
ENST00000337432.9:c.520A>G MANE Select	ENSP00000336701.4:p.Thr174Ala
ENST00000337432.8:c.520A>G	ENSP00000336701.4:p.Thr174Ala
ENST00000413590.5:c.158A>G
ENST00000425173.5:c.316A>G	ENSP00000407282.1:p.Thr106Ala
ENST00000461271.5:c.169A>G	ENSP00000464056.1:p.Thr57Ala
ENST00000475762.5:c.*1223A>G	ENSP00000432421.1:n.*1223A>G
ENST00000482007.5:c.404+1619A>G	ENSP00000433332.1:n.404+1619A>G
ENST00000487525.5:c.404+1619A>G	ENSP00000431637.1:n.404+1619A>G
ENST00000487921.5:n.432A>G
ENST00000583539.5:c.520A>G	ENSP00000463121.1:p.Thr174Ala
ENST00000584617.5:c.242A>G
ENST00000622327.4:c.256A>G	ENSP00000482326.1:p.Thr86Ala
NM_058216.2:c.520A>G	NP_478123.1:p.Thr174Ala
NR_103872.1:n.475+1619A>G
XM_006722001.2:c.520A>G	XP_006722064.1:p.Thr174Ala
XM_006722002.2:c.520A>G	XP_006722065.1:p.Thr174Ala
XM_006722004.2:c.169A>G	XP_006722067.1:p.Thr57Ala
XM_006722005.2:c.169A>G	XP_006722068.1:p.Thr57Ala
XM_011525092.1:c.169A>G	XP_011523394.1:p.Thr57Ala
XM_011525093.1:c.169A>G	XP_011523395.1:p.Thr57Ala
XM_011525094.1:c.169A>G	XP_011523396.1:p.Thr57Ala
XR_934513.1:n.593A>G
XR_934514.1:n.593A>G
XM_006722001.4:c.520A>G	XP_006722064.1:p.Thr174Ala
XM_006722002.4:c.520A>G	XP_006722065.1:p.Thr174Ala
XM_006722004.3:c.169A>G	XP_006722067.1:p.Thr57Ala
XM_006722005.3:c.169A>G	XP_006722068.1:p.Thr57Ala
XM_011525092.2:c.169A>G	XP_011523394.1:p.Thr57Ala
XM_011525093.2:c.169A>G	XP_011523395.1:p.Thr57Ala
XM_011525094.2:c.169A>G	XP_011523396.1:p.Thr57Ala
XM_017024914.1:c.169A>G	XP_016880403.1:p.Thr57Ala
XM_017024915.1:c.169A>G	XP_016880404.1:p.Thr57Ala
XM_017024916.1:c.169A>G	XP_016880405.1:p.Thr57Ala
XM_017024917.1:c.169A>G	XP_016880406.1:p.Thr57Ala
XM_017024918.2:c.169A>G	XP_016880407.1:p.Thr57Ala
XM_017024919.1:c.169A>G	XP_016880408.1:p.Thr57Ala
XR_934513.3:n.1024A>G
XR_934514.3:n.1024A>G
NM_058216.3:c.520A>G MANE Select	NP_478123.1:p.Thr174Ala
NR_103872.2:n.446+1619A>G