Canonical Allele Identifier: CA400349839

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 627998
• ClinVar RCV Id: RCV000772272
• dbSNP Id: rs1567794382
• MyVariant Identifiers: chr17:g.56780651A>C (hg19) ; chr17:g.58703290A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703290A>C , CM000679.2:g.58703290A>C	GRCh38
NC_000017.10:g.56780651A>C , CM000679.1:g.56780651A>C	GRCh37
NC_000017.9:g.54135650A>C	NCBI36
NG_023199.1:g.15689A>C , LRG_314:g.15689A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.315A>C	ENSP00000464056.2:p.Gln105His
ENST00000697677.1:n.1747A>C
ENST00000697678.1:n.568A>C
ENST00000697679.1:n.1740A>C
ENST00000697680.1:c.*1530A>C	ENSP00000513392.1:n.*1530A>C
ENST00000697681.1:c.*1682A>C	ENSP00000513393.1:n.*1682A>C
ENST00000697683.1:c.*1530A>C	ENSP00000513395.1:n.*1530A>C
ENST00000697684.1:n.726A>C
ENST00000697685.1:c.*1363A>C	ENSP00000513396.1:n.*1363A>C
ENST00000697686.1:c.315A>C	ENSP00000513397.1:p.Gln105His
ENST00000697687.1:n.545A>C
ENST00000697688.1:n.712A>C
ENST00000697689.1:c.*1202A>C	ENSP00000513398.1:n.*1202A>C
ENST00000697690.1:c.666A>C	ENSP00000513399.1:p.Gln222His
ENST00000697691.1:c.*638A>C	ENSP00000513400.1:n.*638A>C
ENST00000697692.1:c.*678A>C	ENSP00000513401.1:n.*678A>C
ENST00000697694.1:c.315A>C	ENSP00000513402.1:p.Gln105His
ENST00000697695.1:n.1273A>C
ENST00000337432.9:c.666A>C MANE Select	ENSP00000336701.4:p.Gln222His
ENST00000337432.8:c.666A>C	ENSP00000336701.4:p.Gln222His
ENST00000413590.5:c.304A>C
ENST00000425173.5:c.462A>C	ENSP00000407282.1:p.Gln154His
ENST00000461271.5:c.315A>C	ENSP00000464056.1:p.Gln105His
ENST00000475762.5:c.*1369A>C	ENSP00000432421.1:n.*1369A>C
ENST00000482007.5:c.*94A>C	ENSP00000433332.1:n.*94A>C
ENST00000487525.5:c.*94A>C	ENSP00000431637.1:n.*94A>C
ENST00000487921.5:n.578A>C
ENST00000583539.5:c.666A>C	ENSP00000463121.1:p.Gln222His
ENST00000584617.5:c.388A>C
NM_058216.2:c.666A>C	NP_478123.1:p.Gln222His
NR_103872.1:n.570A>C
XM_006722001.2:c.666A>C	XP_006722064.1:p.Gln222His
XM_006722002.2:c.666A>C	XP_006722065.1:p.Gln222His
XM_006722004.2:c.315A>C	XP_006722067.1:p.Gln105His
XM_006722005.2:c.315A>C	XP_006722068.1:p.Gln105His
XM_011525092.1:c.315A>C	XP_011523394.1:p.Gln105His
XM_011525093.1:c.315A>C	XP_011523395.1:p.Gln105His
XM_011525094.1:c.315A>C	XP_011523396.1:p.Gln105His
XR_934513.1:n.739A>C
XR_934514.1:n.739A>C
XM_006722001.4:c.666A>C	XP_006722064.1:p.Gln222His
XM_006722002.4:c.666A>C	XP_006722065.1:p.Gln222His
XM_006722004.3:c.315A>C	XP_006722067.1:p.Gln105His
XM_006722005.3:c.315A>C	XP_006722068.1:p.Gln105His
XM_011525092.2:c.315A>C	XP_011523394.1:p.Gln105His
XM_011525093.2:c.315A>C	XP_011523395.1:p.Gln105His
XM_011525094.2:c.315A>C	XP_011523396.1:p.Gln105His
XM_017024914.1:c.315A>C	XP_016880403.1:p.Gln105His
XM_017024915.1:c.315A>C	XP_016880404.1:p.Gln105His
XM_017024916.1:c.315A>C	XP_016880405.1:p.Gln105His
XM_017024917.1:c.315A>C	XP_016880406.1:p.Gln105His
XM_017024918.2:c.315A>C	XP_016880407.1:p.Gln105His
XM_017024919.1:c.315A>C	XP_016880408.1:p.Gln105His
XR_934513.3:n.1170A>C
XR_934514.3:n.1170A>C
NM_058216.3:c.666A>C MANE Select	NP_478123.1:p.Gln222His
NR_103872.2:n.541A>C