Canonical Allele Identifier: CA501075922

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 492398
• ClinVar RCV Id: RCV000583605 ; RCV001860099
• dbSNP Id: rs587781287
• MyVariant Identifiers: chr17:g.56801451C>A (hg19) ; chr17:g.58724090C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58724090C>A , CM000679.2:g.58724090C>A	GRCh38
NC_000017.10:g.56801451C>A , CM000679.1:g.56801451C>A	GRCh37
NC_000017.9:g.54156450C>A	NCBI36
NG_023199.1:g.36489C>A , LRG_314:g.36489C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.604C>A	ENSP00000464056.2:p.Arg202=
ENST00000697680.1:c.*1919C>A	ENSP00000513392.1:n.*1919C>A
ENST00000697681.1:c.*2116C>A	ENSP00000513393.1:n.*2116C>A
ENST00000697683.1:c.*1819C>A	ENSP00000513395.1:n.*1819C>A
ENST00000697684.1:n.1015C>A
ENST00000697685.1:c.*1652C>A	ENSP00000513396.1:n.*1652C>A
ENST00000697686.1:c.604C>A	ENSP00000513397.1:p.Arg202=
ENST00000697687.1:n.834C>A
ENST00000697688.1:n.1001C>A
ENST00000697689.1:c.*1440+3278C>A	ENSP00000513398.1:n.*1440+3278C>A
ENST00000697690.1:c.904+3278C>A	ENSP00000513399.1:n.904+3278C>A
ENST00000697691.1:c.*927C>A	ENSP00000513400.1:n.*927C>A
ENST00000697692.1:c.*967C>A	ENSP00000513401.1:n.*967C>A
ENST00000697694.1:c.604C>A	ENSP00000513402.1:p.Arg202=
ENST00000697695.1:n.1562C>A
ENST00000337432.9:c.955C>A MANE Select	ENSP00000336701.4:p.Arg319=
ENST00000337432.8:c.955C>A	ENSP00000336701.4:p.Arg319=
ENST00000413590.5:c.593C>A
ENST00000475762.5:c.*1591C>A	ENSP00000432421.1:n.*1591C>A
ENST00000482007.5:c.*383C>A	ENSP00000433332.1:n.*383C>A
ENST00000487525.5:c.*528C>A	ENSP00000431637.1:n.*528C>A
ENST00000578151.1:n.239+3278C>A
ENST00000581221.5:n.470C>A
ENST00000583539.5:c.955C>A	ENSP00000463121.1:p.Arg319=
ENST00000584617.5:c.677C>A
ENST00000584804.1:c.199+3278C>A	ENSP00000463658.1:n.199+3278C>A
NM_058216.2:c.955C>A	NP_478123.1:p.Arg319=
NR_103872.1:n.859C>A
XM_006722001.2:c.955C>A	XP_006722064.1:p.Arg319=
XM_006722002.2:c.904+3278C>A	XP_006722065.1:n.904+3278C>A
XM_006722004.2:c.604C>A	XP_006722067.1:p.Arg202=
XM_006722005.2:c.604C>A	XP_006722068.1:p.Arg202=
XM_011525092.1:c.604C>A	XP_011523394.1:p.Arg202=
XM_011525093.1:c.604C>A	XP_011523395.1:p.Arg202=
XM_011525094.1:c.604C>A	XP_011523396.1:p.Arg202=
XR_934513.1:n.1173C>A
XR_934514.1:n.1173C>A
XM_006722001.4:c.955C>A	XP_006722064.1:p.Arg319=
XM_006722002.4:c.904+3278C>A	XP_006722065.1:n.904+3278C>A
XM_006722004.3:c.604C>A	XP_006722067.1:p.Arg202=
XM_006722005.3:c.604C>A	XP_006722068.1:p.Arg202=
XM_011525092.2:c.604C>A	XP_011523394.1:p.Arg202=
XM_011525093.2:c.604C>A	XP_011523395.1:p.Arg202=
XM_011525094.2:c.604C>A	XP_011523396.1:p.Arg202=
XM_017024914.1:c.604C>A	XP_016880403.1:p.Arg202=
XM_017024915.1:c.604C>A	XP_016880404.1:p.Arg202=
XM_017024916.1:c.604C>A	XP_016880405.1:p.Arg202=
XM_017024917.1:c.604C>A	XP_016880406.1:p.Arg202=
XM_017024918.2:c.604C>A	XP_016880407.1:p.Arg202=
XM_017024919.1:c.553+3278C>A	XP_016880408.1:n.553+3278C>A
XR_934513.3:n.1604C>A
XR_934514.3:n.1604C>A
NM_058216.3:c.955C>A MANE Select	NP_478123.1:p.Arg319=
NR_103872.2:n.830C>A