Canonical Allele Identifier: CA400350161

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 484735
• ClinVar RCV Id: RCV000570909
• dbSNP Id: rs1555597252
• MyVariant Identifiers: chr17:g.56780688A>G (hg19) ; chr17:g.58703327A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703327A>G , CM000679.2:g.58703327A>G	GRCh38
NC_000017.10:g.56780688A>G , CM000679.1:g.56780688A>G	GRCh37
NC_000017.9:g.54135687A>G	NCBI36
NG_023199.1:g.15726A>G , LRG_314:g.15726A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.352A>G	ENSP00000464056.2:p.Lys118Glu
ENST00000697677.1:n.1784A>G
ENST00000697678.1:n.605A>G
ENST00000697679.1:n.1777A>G
ENST00000697680.1:c.*1567A>G	ENSP00000513392.1:n.*1567A>G
ENST00000697681.1:c.*1719A>G	ENSP00000513393.1:n.*1719A>G
ENST00000697683.1:c.*1567A>G	ENSP00000513395.1:n.*1567A>G
ENST00000697684.1:n.763A>G
ENST00000697685.1:c.*1400A>G	ENSP00000513396.1:n.*1400A>G
ENST00000697686.1:c.352A>G	ENSP00000513397.1:p.Lys118Glu
ENST00000697687.1:n.582A>G
ENST00000697688.1:n.749A>G
ENST00000697689.1:c.*1239A>G	ENSP00000513398.1:n.*1239A>G
ENST00000697690.1:c.703A>G	ENSP00000513399.1:p.Lys235Glu
ENST00000697691.1:c.*675A>G	ENSP00000513400.1:n.*675A>G
ENST00000697692.1:c.*715A>G	ENSP00000513401.1:n.*715A>G
ENST00000697694.1:c.352A>G	ENSP00000513402.1:p.Lys118Glu
ENST00000697695.1:n.1310A>G
ENST00000337432.9:c.703A>G MANE Select	ENSP00000336701.4:p.Lys235Glu
ENST00000337432.8:c.703A>G	ENSP00000336701.4:p.Lys235Glu
ENST00000413590.5:c.341A>G
ENST00000425173.5:c.499A>G	ENSP00000407282.1:p.Lys167Glu
ENST00000461271.5:c.352A>G	ENSP00000464056.1:p.Lys118Glu
ENST00000475762.5:c.*1406A>G	ENSP00000432421.1:n.*1406A>G
ENST00000482007.5:c.*131A>G	ENSP00000433332.1:n.*131A>G
ENST00000487525.5:c.*131A>G	ENSP00000431637.1:n.*131A>G
ENST00000487921.5:n.615A>G
ENST00000583539.5:c.703A>G	ENSP00000463121.1:p.Lys235Glu
ENST00000584617.5:c.425A>G
NM_058216.2:c.703A>G	NP_478123.1:p.Lys235Glu
NR_103872.1:n.607A>G
XM_006722001.2:c.703A>G	XP_006722064.1:p.Lys235Glu
XM_006722002.2:c.703A>G	XP_006722065.1:p.Lys235Glu
XM_006722004.2:c.352A>G	XP_006722067.1:p.Lys118Glu
XM_006722005.2:c.352A>G	XP_006722068.1:p.Lys118Glu
XM_011525092.1:c.352A>G	XP_011523394.1:p.Lys118Glu
XM_011525093.1:c.352A>G	XP_011523395.1:p.Lys118Glu
XM_011525094.1:c.352A>G	XP_011523396.1:p.Lys118Glu
XR_934513.1:n.776A>G
XR_934514.1:n.776A>G
XM_006722001.4:c.703A>G	XP_006722064.1:p.Lys235Glu
XM_006722002.4:c.703A>G	XP_006722065.1:p.Lys235Glu
XM_006722004.3:c.352A>G	XP_006722067.1:p.Lys118Glu
XM_006722005.3:c.352A>G	XP_006722068.1:p.Lys118Glu
XM_011525092.2:c.352A>G	XP_011523394.1:p.Lys118Glu
XM_011525093.2:c.352A>G	XP_011523395.1:p.Lys118Glu
XM_011525094.2:c.352A>G	XP_011523396.1:p.Lys118Glu
XM_017024914.1:c.352A>G	XP_016880403.1:p.Lys118Glu
XM_017024915.1:c.352A>G	XP_016880404.1:p.Lys118Glu
XM_017024916.1:c.352A>G	XP_016880405.1:p.Lys118Glu
XM_017024917.1:c.352A>G	XP_016880406.1:p.Lys118Glu
XM_017024918.2:c.352A>G	XP_016880407.1:p.Lys118Glu
XM_017024919.1:c.352A>G	XP_016880408.1:p.Lys118Glu
XR_934513.3:n.1207A>G
XR_934514.3:n.1207A>G
NM_058216.3:c.703A>G MANE Select	NP_478123.1:p.Lys235Glu
NR_103872.2:n.578A>G