Canonical Allele Identifier: CA400343816

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 628696
• ClinVar RCV Id: RCV000773357 ; RCV000793265 ; RCV003465693
• dbSNP Id: rs1567788274
• MyVariant Identifiers: chr17:g.56774065C>T (hg19) ; chr17:g.58696704C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58696704C>T , CM000679.2:g.58696704C>T	GRCh38
NC_000017.10:g.56774065C>T , CM000679.1:g.56774065C>T	GRCh37
NC_000017.9:g.54129064C>T	NCBI36
NG_023199.1:g.9103C>T , LRG_314:g.9103C>T
NG_047169.1:g.376G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.65C>T	ENSP00000464056.2:p.Ala22Val
ENST00000697675.1:n.3013C>T
ENST00000697676.1:n.476C>T
ENST00000697677.1:n.1497C>T
ENST00000697678.1:n.318C>T
ENST00000697679.1:n.1490C>T
ENST00000697680.1:c.*1280C>T	ENSP00000513392.1:n.*1280C>T
ENST00000697681.1:c.*1307C>T	ENSP00000513393.1:n.*1307C>T
ENST00000697683.1:c.*1280C>T	ENSP00000513395.1:n.*1280C>T
ENST00000697684.1:n.476C>T
ENST00000697685.1:c.*1268+1515C>T	ENSP00000513396.1:n.*1268+1515C>T
ENST00000697686.1:c.65C>T	ENSP00000513397.1:p.Ala22Val
ENST00000697687.1:n.450+1515C>T
ENST00000697688.1:n.462C>T
ENST00000697689.1:c.*1107+1515C>T	ENSP00000513398.1:n.*1107+1515C>T
ENST00000697690.1:c.416C>T	ENSP00000513399.1:p.Ala139Val
ENST00000697691.1:c.*388C>T	ENSP00000513400.1:n.*388C>T
ENST00000697692.1:c.*428C>T	ENSP00000513401.1:n.*428C>T
ENST00000697694.1:c.65C>T	ENSP00000513402.1:p.Ala22Val
ENST00000697695.1:n.1023C>T
ENST00000337432.9:c.416C>T MANE Select	ENSP00000336701.4:p.Ala139Val
ENST00000337432.8:c.416C>T	ENSP00000336701.4:p.Ala139Val
ENST00000413590.5:c.54C>T
ENST00000425173.5:c.212C>T	ENSP00000407282.1:p.Ala71Val
ENST00000461271.5:c.65C>T	ENSP00000464056.1:p.Ala22Val
ENST00000475762.5:c.*1119C>T	ENSP00000432421.1:n.*1119C>T
ENST00000482007.5:c.404+1515C>T	ENSP00000433332.1:n.404+1515C>T
ENST00000487525.5:c.404+1515C>T	ENSP00000431637.1:n.404+1515C>T
ENST00000487921.5:n.328C>T
ENST00000583539.5:c.416C>T	ENSP00000463121.1:p.Ala139Val
ENST00000584617.5:c.138C>T
ENST00000622327.4:c.152C>T	ENSP00000482326.1:p.Ala51Val
NM_058216.2:c.416C>T	NP_478123.1:p.Ala139Val
NR_103872.1:n.475+1515C>T
XM_006722001.2:c.416C>T	XP_006722064.1:p.Ala139Val
XM_006722002.2:c.416C>T	XP_006722065.1:p.Ala139Val
XM_006722004.2:c.65C>T	XP_006722067.1:p.Ala22Val
XM_006722005.2:c.65C>T	XP_006722068.1:p.Ala22Val
XM_011525092.1:c.65C>T	XP_011523394.1:p.Ala22Val
XM_011525093.1:c.65C>T	XP_011523395.1:p.Ala22Val
XM_011525094.1:c.65C>T	XP_011523396.1:p.Ala22Val
XR_934513.1:n.489C>T
XR_934514.1:n.489C>T
XM_006722001.4:c.416C>T	XP_006722064.1:p.Ala139Val
XM_006722002.4:c.416C>T	XP_006722065.1:p.Ala139Val
XM_006722004.3:c.65C>T	XP_006722067.1:p.Ala22Val
XM_006722005.3:c.65C>T	XP_006722068.1:p.Ala22Val
XM_011525092.2:c.65C>T	XP_011523394.1:p.Ala22Val
XM_011525093.2:c.65C>T	XP_011523395.1:p.Ala22Val
XM_011525094.2:c.65C>T	XP_011523396.1:p.Ala22Val
XM_017024914.1:c.65C>T	XP_016880403.1:p.Ala22Val
XM_017024915.1:c.65C>T	XP_016880404.1:p.Ala22Val
XM_017024916.1:c.65C>T	XP_016880405.1:p.Ala22Val
XM_017024917.1:c.65C>T	XP_016880406.1:p.Ala22Val
XM_017024918.2:c.65C>T	XP_016880407.1:p.Ala22Val
XM_017024919.1:c.65C>T	XP_016880408.1:p.Ala22Val
XR_934513.3:n.920C>T
XR_934514.3:n.920C>T
NM_058216.3:c.416C>T MANE Select	NP_478123.1:p.Ala139Val
NR_103872.2:n.446+1515C>T