Canonical Allele Identifier: CA400364821

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 859251
• ClinVar RCV Id: RCV001065317
• dbSNP Id: rs1436204606
• MyVariant Identifiers: chr17:g.56809843A>G (hg19) ; chr17:g.58732482A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58732482A>G , CM000679.2:g.58732482A>G	GRCh38
NC_000017.10:g.56809843A>G , CM000679.1:g.56809843A>G	GRCh37
NC_000017.9:g.54164842A>G	NCBI36
NG_023199.1:g.44881A>G , LRG_314:g.44881A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.615-2A>G	ENSP00000464056.2:n.615-2A>G
ENST00000697680.1:c.*1930-2A>G	ENSP00000513392.1:n.*1930-2A>G
ENST00000697681.1:c.*2127-2A>G	ENSP00000513393.1:n.*2127-2A>G
ENST00000697683.1:c.*1902-2A>G	ENSP00000513395.1:n.*1902-2A>G
ENST00000697685.1:c.*1663-2A>G	ENSP00000513396.1:n.*1663-2A>G
ENST00000697686.1:c.737-2A>G	ENSP00000513397.1:n.737-2A>G
ENST00000697689.1:c.*1441-1636A>G	ENSP00000513398.1:n.*1441-1636A>G
ENST00000697690.1:c.905-1636A>G	ENSP00000513399.1:n.905-1636A>G
ENST00000697691.1:c.*938-2A>G	ENSP00000513400.1:n.*938-2A>G
ENST00000697692.1:c.*978-2A>G	ENSP00000513401.1:n.*978-2A>G
ENST00000697694.1:c.615-2A>G	ENSP00000513402.1:n.615-2A>G
ENST00000697695.1:n.1573-2A>G
ENST00000337432.9:c.966-2A>G MANE Select	ENSP00000336701.4:n.966-2A>G
ENST00000337432.8:c.966-2A>G	ENSP00000336701.4:n.966-2A>G
ENST00000413590.5:c.605A>G
ENST00000461706.1:n.151A>G
ENST00000475762.5:c.*1602-2A>G	ENSP00000432421.1:n.*1602-2A>G
ENST00000482007.5:c.*394-2A>G	ENSP00000433332.1:n.*394-2A>G
ENST00000487525.5:c.*540A>G	ENSP00000431637.1:n.*540A>G
ENST00000578151.1:n.240-1636A>G
ENST00000581221.5:n.481-2A>G
ENST00000583539.5:c.966-2A>G	ENSP00000463121.1:n.966-2A>G
ENST00000584617.5:c.688-2A>G
ENST00000584804.1:c.200-2A>G	ENSP00000463658.1:n.200-2A>G
NM_058216.2:c.966-2A>G	NP_478123.1:n.966-2A>G
NR_103872.1:n.870-2A>G
XM_006722001.2:c.967A>G	XP_006722064.1:p.Arg323Gly
XM_006722002.2:c.905-2A>G	XP_006722065.1:n.905-2A>G
XM_006722004.2:c.616A>G	XP_006722067.1:p.Arg206Gly
XM_006722005.2:c.616A>G	XP_006722068.1:p.Arg206Gly
XM_011525092.1:c.616A>G	XP_011523394.1:p.Arg206Gly
XM_011525093.1:c.616A>G	XP_011523395.1:p.Arg206Gly
XM_011525094.1:c.616A>G	XP_011523396.1:p.Arg206Gly
XR_934513.1:n.1184-2A>G
XR_934514.1:n.1185A>G
XR_934886.1:n.149+5589T>C
XM_006722001.4:c.967A>G	XP_006722064.1:p.Arg323Gly
XM_006722002.4:c.905-2A>G	XP_006722065.1:n.905-2A>G
XM_006722004.3:c.616A>G	XP_006722067.1:p.Arg206Gly
XM_006722005.3:c.616A>G	XP_006722068.1:p.Arg206Gly
XM_011525092.2:c.616A>G	XP_011523394.1:p.Arg206Gly
XM_011525093.2:c.616A>G	XP_011523395.1:p.Arg206Gly
XM_011525094.2:c.616A>G	XP_011523396.1:p.Arg206Gly
XM_017024914.1:c.615-2A>G	XP_016880403.1:n.615-2A>G
XM_017024915.1:c.615-2A>G	XP_016880404.1:n.615-2A>G
XM_017024916.1:c.615-2A>G	XP_016880405.1:n.615-2A>G
XM_017024917.1:c.615-2A>G	XP_016880406.1:n.615-2A>G
XM_017024918.2:c.615-2A>G	XP_016880407.1:n.615-2A>G
XM_017024919.1:c.554-2A>G	XP_016880408.1:n.554-2A>G
XR_934513.3:n.1615-2A>G
XR_934514.3:n.1616A>G
XR_934886.2:n.149+5589T>C
NM_058216.3:c.966-2A>G MANE Select	NP_478123.1:n.966-2A>G
NR_103872.2:n.841-2A>G