Canonical Allele Identifier: CA400343958

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 1739327
• ClinVar RCV Id: RCV002330102 ; RCV004049900
• dbSNP Id: rs2143744121
• gnomAD v4: 17-58696715-C-T
• MyVariant Identifiers: chr17:g.56774076C>T (hg19) ; chr17:g.58696715C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58696715C>T , CM000679.2:g.58696715C>T	GRCh38
NC_000017.10:g.56774076C>T , CM000679.1:g.56774076C>T	GRCh37
NC_000017.9:g.54129075C>T	NCBI36
NG_023199.1:g.9114C>T , LRG_314:g.9114C>T
NG_047169.1:g.365G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.76C>T	ENSP00000464056.2:p.Gln26Ter
ENST00000697675.1:n.3024C>T
ENST00000697676.1:n.487C>T
ENST00000697677.1:n.1508C>T
ENST00000697678.1:n.329C>T
ENST00000697679.1:n.1501C>T
ENST00000697680.1:c.*1291C>T	ENSP00000513392.1:n.*1291C>T
ENST00000697681.1:c.*1318C>T	ENSP00000513393.1:n.*1318C>T
ENST00000697683.1:c.*1291C>T	ENSP00000513395.1:n.*1291C>T
ENST00000697684.1:n.487C>T
ENST00000697685.1:c.*1268+1526C>T	ENSP00000513396.1:n.*1268+1526C>T
ENST00000697686.1:c.76C>T	ENSP00000513397.1:p.Gln26Ter
ENST00000697687.1:n.450+1526C>T
ENST00000697688.1:n.473C>T
ENST00000697689.1:c.*1107+1526C>T	ENSP00000513398.1:n.*1107+1526C>T
ENST00000697690.1:c.427C>T	ENSP00000513399.1:p.Gln143Ter
ENST00000697691.1:c.*399C>T	ENSP00000513400.1:n.*399C>T
ENST00000697692.1:c.*439C>T	ENSP00000513401.1:n.*439C>T
ENST00000697694.1:c.76C>T	ENSP00000513402.1:p.Gln26Ter
ENST00000697695.1:n.1034C>T
ENST00000337432.9:c.427C>T MANE Select	ENSP00000336701.4:p.Gln143Ter
ENST00000337432.8:c.427C>T	ENSP00000336701.4:p.Gln143Ter
ENST00000413590.5:c.65C>T
ENST00000425173.5:c.223C>T	ENSP00000407282.1:p.Gln75Ter
ENST00000461271.5:c.76C>T	ENSP00000464056.1:p.Gln26Ter
ENST00000475762.5:c.*1130C>T	ENSP00000432421.1:n.*1130C>T
ENST00000482007.5:c.404+1526C>T	ENSP00000433332.1:n.404+1526C>T
ENST00000487525.5:c.404+1526C>T	ENSP00000431637.1:n.404+1526C>T
ENST00000487921.5:n.339C>T
ENST00000583539.5:c.427C>T	ENSP00000463121.1:p.Gln143Ter
ENST00000584617.5:c.149C>T
ENST00000622327.4:c.163C>T	ENSP00000482326.1:p.Gln55Ter
NM_058216.2:c.427C>T	NP_478123.1:p.Gln143Ter
NR_103872.1:n.475+1526C>T
XM_006722001.2:c.427C>T	XP_006722064.1:p.Gln143Ter
XM_006722002.2:c.427C>T	XP_006722065.1:p.Gln143Ter
XM_006722004.2:c.76C>T	XP_006722067.1:p.Gln26Ter
XM_006722005.2:c.76C>T	XP_006722068.1:p.Gln26Ter
XM_011525092.1:c.76C>T	XP_011523394.1:p.Gln26Ter
XM_011525093.1:c.76C>T	XP_011523395.1:p.Gln26Ter
XM_011525094.1:c.76C>T	XP_011523396.1:p.Gln26Ter
XR_934513.1:n.500C>T
XR_934514.1:n.500C>T
XM_006722001.4:c.427C>T	XP_006722064.1:p.Gln143Ter
XM_006722002.4:c.427C>T	XP_006722065.1:p.Gln143Ter
XM_006722004.3:c.76C>T	XP_006722067.1:p.Gln26Ter
XM_006722005.3:c.76C>T	XP_006722068.1:p.Gln26Ter
XM_011525092.2:c.76C>T	XP_011523394.1:p.Gln26Ter
XM_011525093.2:c.76C>T	XP_011523395.1:p.Gln26Ter
XM_011525094.2:c.76C>T	XP_011523396.1:p.Gln26Ter
XM_017024914.1:c.76C>T	XP_016880403.1:p.Gln26Ter
XM_017024915.1:c.76C>T	XP_016880404.1:p.Gln26Ter
XM_017024916.1:c.76C>T	XP_016880405.1:p.Gln26Ter
XM_017024917.1:c.76C>T	XP_016880406.1:p.Gln26Ter
XM_017024918.2:c.76C>T	XP_016880407.1:p.Gln26Ter
XM_017024919.1:c.76C>T	XP_016880408.1:p.Gln26Ter
XR_934513.3:n.931C>T
XR_934514.3:n.931C>T
NM_058216.3:c.427C>T MANE Select	NP_478123.1:p.Gln143Ter
NR_103872.2:n.446+1526C>T