Canonical Allele Identifier: CA400349517

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 2974391
• ClinVar RCV Id: RCV003836029
• MyVariant Identifiers: chr17:g.56780622T>C (hg19) ; chr17:g.58703261T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703261T>C , CM000679.2:g.58703261T>C	GRCh38
NC_000017.10:g.56780622T>C , CM000679.1:g.56780622T>C	GRCh37
NC_000017.9:g.54135621T>C	NCBI36
NG_023199.1:g.15660T>C , LRG_314:g.15660T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.286T>C	ENSP00000464056.2:p.Cys96Arg
ENST00000697677.1:n.1718T>C
ENST00000697678.1:n.539T>C
ENST00000697679.1:n.1711T>C
ENST00000697680.1:c.*1501T>C	ENSP00000513392.1:n.*1501T>C
ENST00000697681.1:c.*1653T>C	ENSP00000513393.1:n.*1653T>C
ENST00000697683.1:c.*1501T>C	ENSP00000513395.1:n.*1501T>C
ENST00000697684.1:n.697T>C
ENST00000697685.1:c.*1334T>C	ENSP00000513396.1:n.*1334T>C
ENST00000697686.1:c.286T>C	ENSP00000513397.1:p.Cys96Arg
ENST00000697687.1:n.516T>C
ENST00000697688.1:n.683T>C
ENST00000697689.1:c.*1173T>C	ENSP00000513398.1:n.*1173T>C
ENST00000697690.1:c.637T>C	ENSP00000513399.1:p.Cys213Arg
ENST00000697691.1:c.*609T>C	ENSP00000513400.1:n.*609T>C
ENST00000697692.1:c.*649T>C	ENSP00000513401.1:n.*649T>C
ENST00000697694.1:c.286T>C	ENSP00000513402.1:p.Cys96Arg
ENST00000697695.1:n.1244T>C
ENST00000337432.9:c.637T>C MANE Select	ENSP00000336701.4:p.Cys213Arg
ENST00000337432.8:c.637T>C	ENSP00000336701.4:p.Cys213Arg
ENST00000413590.5:c.275T>C
ENST00000425173.5:c.433T>C	ENSP00000407282.1:p.Cys145Arg
ENST00000461271.5:c.286T>C	ENSP00000464056.1:p.Cys96Arg
ENST00000475762.5:c.*1340T>C	ENSP00000432421.1:n.*1340T>C
ENST00000482007.5:c.*65T>C	ENSP00000433332.1:n.*65T>C
ENST00000487525.5:c.*65T>C	ENSP00000431637.1:n.*65T>C
ENST00000487921.5:n.549T>C
ENST00000583539.5:c.637T>C	ENSP00000463121.1:p.Cys213Arg
ENST00000584617.5:c.359T>C
NM_058216.2:c.637T>C	NP_478123.1:p.Cys213Arg
NR_103872.1:n.541T>C
XM_006722001.2:c.637T>C	XP_006722064.1:p.Cys213Arg
XM_006722002.2:c.637T>C	XP_006722065.1:p.Cys213Arg
XM_006722004.2:c.286T>C	XP_006722067.1:p.Cys96Arg
XM_006722005.2:c.286T>C	XP_006722068.1:p.Cys96Arg
XM_011525092.1:c.286T>C	XP_011523394.1:p.Cys96Arg
XM_011525093.1:c.286T>C	XP_011523395.1:p.Cys96Arg
XM_011525094.1:c.286T>C	XP_011523396.1:p.Cys96Arg
XR_934513.1:n.710T>C
XR_934514.1:n.710T>C
XM_006722001.4:c.637T>C	XP_006722064.1:p.Cys213Arg
XM_006722002.4:c.637T>C	XP_006722065.1:p.Cys213Arg
XM_006722004.3:c.286T>C	XP_006722067.1:p.Cys96Arg
XM_006722005.3:c.286T>C	XP_006722068.1:p.Cys96Arg
XM_011525092.2:c.286T>C	XP_011523394.1:p.Cys96Arg
XM_011525093.2:c.286T>C	XP_011523395.1:p.Cys96Arg
XM_011525094.2:c.286T>C	XP_011523396.1:p.Cys96Arg
XM_017024914.1:c.286T>C	XP_016880403.1:p.Cys96Arg
XM_017024915.1:c.286T>C	XP_016880404.1:p.Cys96Arg
XM_017024916.1:c.286T>C	XP_016880405.1:p.Cys96Arg
XM_017024917.1:c.286T>C	XP_016880406.1:p.Cys96Arg
XM_017024918.2:c.286T>C	XP_016880407.1:p.Cys96Arg
XM_017024919.1:c.286T>C	XP_016880408.1:p.Cys96Arg
XR_934513.3:n.1141T>C
XR_934514.3:n.1141T>C
NM_058216.3:c.637T>C MANE Select	NP_478123.1:p.Cys213Arg
NR_103872.2:n.512T>C