Canonical Allele Identifier: CA400349854

Gene: RAD51C

Linked Data

• dbSNP Id: rs2143800542
• gnomAD v4: 17-58703292-T-A
• MyVariant Identifiers: chr17:g.56780653T>A (hg19) ; chr17:g.58703292T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703292T>A , CM000679.2:g.58703292T>A	GRCh38
NC_000017.10:g.56780653T>A , CM000679.1:g.56780653T>A	GRCh37
NC_000017.9:g.54135652T>A	NCBI36
NG_023199.1:g.15691T>A , LRG_314:g.15691T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.317T>A	ENSP00000464056.2:p.Val106Asp
ENST00000697677.1:n.1749T>A
ENST00000697678.1:n.570T>A
ENST00000697679.1:n.1742T>A
ENST00000697680.1:c.*1532T>A	ENSP00000513392.1:n.*1532T>A
ENST00000697681.1:c.*1684T>A	ENSP00000513393.1:n.*1684T>A
ENST00000697683.1:c.*1532T>A	ENSP00000513395.1:n.*1532T>A
ENST00000697684.1:n.728T>A
ENST00000697685.1:c.*1365T>A	ENSP00000513396.1:n.*1365T>A
ENST00000697686.1:c.317T>A	ENSP00000513397.1:p.Val106Asp
ENST00000697687.1:n.547T>A
ENST00000697688.1:n.714T>A
ENST00000697689.1:c.*1204T>A	ENSP00000513398.1:n.*1204T>A
ENST00000697690.1:c.668T>A	ENSP00000513399.1:p.Val223Asp
ENST00000697691.1:c.*640T>A	ENSP00000513400.1:n.*640T>A
ENST00000697692.1:c.*680T>A	ENSP00000513401.1:n.*680T>A
ENST00000697694.1:c.317T>A	ENSP00000513402.1:p.Val106Asp
ENST00000697695.1:n.1275T>A
ENST00000337432.9:c.668T>A MANE Select	ENSP00000336701.4:p.Val223Asp
ENST00000337432.8:c.668T>A	ENSP00000336701.4:p.Val223Asp
ENST00000413590.5:c.306T>A
ENST00000425173.5:c.464T>A	ENSP00000407282.1:p.Val155Asp
ENST00000461271.5:c.317T>A	ENSP00000464056.1:p.Val106Asp
ENST00000475762.5:c.*1371T>A	ENSP00000432421.1:n.*1371T>A
ENST00000482007.5:c.*96T>A	ENSP00000433332.1:n.*96T>A
ENST00000487525.5:c.*96T>A	ENSP00000431637.1:n.*96T>A
ENST00000487921.5:n.580T>A
ENST00000583539.5:c.668T>A	ENSP00000463121.1:p.Val223Asp
ENST00000584617.5:c.390T>A
NM_058216.2:c.668T>A	NP_478123.1:p.Val223Asp
NR_103872.1:n.572T>A
XM_006722001.2:c.668T>A	XP_006722064.1:p.Val223Asp
XM_006722002.2:c.668T>A	XP_006722065.1:p.Val223Asp
XM_006722004.2:c.317T>A	XP_006722067.1:p.Val106Asp
XM_006722005.2:c.317T>A	XP_006722068.1:p.Val106Asp
XM_011525092.1:c.317T>A	XP_011523394.1:p.Val106Asp
XM_011525093.1:c.317T>A	XP_011523395.1:p.Val106Asp
XM_011525094.1:c.317T>A	XP_011523396.1:p.Val106Asp
XR_934513.1:n.741T>A
XR_934514.1:n.741T>A
XM_006722001.4:c.668T>A	XP_006722064.1:p.Val223Asp
XM_006722002.4:c.668T>A	XP_006722065.1:p.Val223Asp
XM_006722004.3:c.317T>A	XP_006722067.1:p.Val106Asp
XM_006722005.3:c.317T>A	XP_006722068.1:p.Val106Asp
XM_011525092.2:c.317T>A	XP_011523394.1:p.Val106Asp
XM_011525093.2:c.317T>A	XP_011523395.1:p.Val106Asp
XM_011525094.2:c.317T>A	XP_011523396.1:p.Val106Asp
XM_017024914.1:c.317T>A	XP_016880403.1:p.Val106Asp
XM_017024915.1:c.317T>A	XP_016880404.1:p.Val106Asp
XM_017024916.1:c.317T>A	XP_016880405.1:p.Val106Asp
XM_017024917.1:c.317T>A	XP_016880406.1:p.Val106Asp
XM_017024918.2:c.317T>A	XP_016880407.1:p.Val106Asp
XM_017024919.1:c.317T>A	XP_016880408.1:p.Val106Asp
XR_934513.3:n.1172T>A
XR_934514.3:n.1172T>A
NM_058216.3:c.668T>A MANE Select	NP_478123.1:p.Val223Asp
NR_103872.2:n.543T>A