Canonical Allele Identifier: CA400361294

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 1502314
• ClinVar RCV Id: RCV002010952
• dbSNP Id: rs2143961390
• MyVariant Identifiers: chr17:g.56801406A>G (hg19) ; chr17:g.58724045A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58724045A>G , CM000679.2:g.58724045A>G	GRCh38
NC_000017.10:g.56801406A>G , CM000679.1:g.56801406A>G	GRCh37
NC_000017.9:g.54156405A>G	NCBI36
NG_023199.1:g.36444A>G , LRG_314:g.36444A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.559A>G	ENSP00000464056.2:p.Ser187Gly
ENST00000697680.1:c.*1874A>G	ENSP00000513392.1:n.*1874A>G
ENST00000697681.1:c.*2071A>G	ENSP00000513393.1:n.*2071A>G
ENST00000697683.1:c.*1774A>G	ENSP00000513395.1:n.*1774A>G
ENST00000697684.1:n.970A>G
ENST00000697685.1:c.*1607A>G	ENSP00000513396.1:n.*1607A>G
ENST00000697686.1:c.559A>G	ENSP00000513397.1:p.Ser187Gly
ENST00000697687.1:n.789A>G
ENST00000697688.1:n.956A>G
ENST00000697689.1:c.*1440+3233A>G	ENSP00000513398.1:n.*1440+3233A>G
ENST00000697690.1:c.904+3233A>G	ENSP00000513399.1:n.904+3233A>G
ENST00000697691.1:c.*882A>G	ENSP00000513400.1:n.*882A>G
ENST00000697692.1:c.*922A>G	ENSP00000513401.1:n.*922A>G
ENST00000697694.1:c.559A>G	ENSP00000513402.1:p.Ser187Gly
ENST00000697695.1:n.1517A>G
ENST00000337432.9:c.910A>G MANE Select	ENSP00000336701.4:p.Ser304Gly
ENST00000337432.8:c.910A>G	ENSP00000336701.4:p.Ser304Gly
ENST00000413590.5:c.548A>G
ENST00000475762.5:c.*1546A>G	ENSP00000432421.1:n.*1546A>G
ENST00000482007.5:c.*338A>G	ENSP00000433332.1:n.*338A>G
ENST00000487525.5:c.*483A>G	ENSP00000431637.1:n.*483A>G
ENST00000578151.1:n.239+3233A>G
ENST00000581221.5:n.425A>G
ENST00000583539.5:c.910A>G	ENSP00000463121.1:p.Ser304Gly
ENST00000584617.5:c.632A>G
ENST00000584804.1:c.199+3233A>G	ENSP00000463658.1:n.199+3233A>G
NM_058216.2:c.910A>G	NP_478123.1:p.Ser304Gly
NR_103872.1:n.814A>G
XM_006722001.2:c.910A>G	XP_006722064.1:p.Ser304Gly
XM_006722002.2:c.904+3233A>G	XP_006722065.1:n.904+3233A>G
XM_006722004.2:c.559A>G	XP_006722067.1:p.Ser187Gly
XM_006722005.2:c.559A>G	XP_006722068.1:p.Ser187Gly
XM_011525092.1:c.559A>G	XP_011523394.1:p.Ser187Gly
XM_011525093.1:c.559A>G	XP_011523395.1:p.Ser187Gly
XM_011525094.1:c.559A>G	XP_011523396.1:p.Ser187Gly
XR_934513.1:n.1128A>G
XR_934514.1:n.1128A>G
XM_006722001.4:c.910A>G	XP_006722064.1:p.Ser304Gly
XM_006722002.4:c.904+3233A>G	XP_006722065.1:n.904+3233A>G
XM_006722004.3:c.559A>G	XP_006722067.1:p.Ser187Gly
XM_006722005.3:c.559A>G	XP_006722068.1:p.Ser187Gly
XM_011525092.2:c.559A>G	XP_011523394.1:p.Ser187Gly
XM_011525093.2:c.559A>G	XP_011523395.1:p.Ser187Gly
XM_011525094.2:c.559A>G	XP_011523396.1:p.Ser187Gly
XM_017024914.1:c.559A>G	XP_016880403.1:p.Ser187Gly
XM_017024915.1:c.559A>G	XP_016880404.1:p.Ser187Gly
XM_017024916.1:c.559A>G	XP_016880405.1:p.Ser187Gly
XM_017024917.1:c.559A>G	XP_016880406.1:p.Ser187Gly
XM_017024918.2:c.559A>G	XP_016880407.1:p.Ser187Gly
XM_017024919.1:c.553+3233A>G	XP_016880408.1:n.553+3233A>G
XR_934513.3:n.1559A>G
XR_934514.3:n.1559A>G
NM_058216.3:c.910A>G MANE Select	NP_478123.1:p.Ser304Gly
NR_103872.2:n.785A>G