Canonical Allele Identifier: CA338452

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 216877
• ClinVar RCV Id: RCV000199181
• dbSNP Id: rs1555597210
• MyVariant Identifiers: chr17:g.56780655_56780754dup (hg19) ; chr17:g.56780655_56780754dup100 (hg19) ; chr17:g.58703294_58703393dup (hg38) ; chr17:g.58703294_58703393dup100 (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703294_58703393dup , CM000679.2:g.58703294_58703393dup	GRCh38
NC_000017.10:g.56780655_56780754dup , CM000679.1:g.56780655_56780754dup	GRCh37
NC_000017.9:g.54135654_54135753dup	NCBI36
NG_023199.1:g.15693_15792dup , LRG_314:g.15693_15792dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.319_354+64dup
ENST00000697677.1:n.1751_1850dup
ENST00000697678.1:n.572_607+64dup
ENST00000697679.1:n.1744_1779+64dup
ENST00000697680.1:c.*1534_*1569+64dup
ENST00000697681.1:c.*1686_*1721+64dup
ENST00000697683.1:c.*1534_*1569+64dup
ENST00000697684.1:n.730_765+64dup
ENST00000697685.1:c.*1367_*1402+64dup
ENST00000697686.1:c.319_354+64dup
ENST00000697687.1:n.549_584+64dup
ENST00000697688.1:n.716_751+64dup
ENST00000697689.1:c.*1206_*1241+64dup
ENST00000697690.1:c.670_705+64dup
ENST00000697691.1:c.*642_*677+64dup
ENST00000697692.1:c.*682_*717+64dup
ENST00000697694.1:c.319_354+64dup
ENST00000697695.1:n.1277_1312+64dup
ENST00000337432.9:c.670_705+64dup
ENST00000337432.8:c.670_705+64dup
ENST00000413590.5:c.308_343+64dup
ENST00000425173.5:c.466_501+64dup
ENST00000461271.5:c.319_354+64dup
ENST00000475762.5:c.*1373_*1408+64dup
ENST00000482007.5:c.*98_*133+64dup
ENST00000487525.5:c.*98_*133+64dup
ENST00000487921.5:n.582_617+64dup
ENST00000583539.5:c.670_705+64dup
ENST00000584617.5:c.392_427+64dup
NM_058216.2:c.670_705+64dup
NR_103872.1:n.574_609+64dup
XM_006722001.2:c.670_705+64dup
XM_006722002.2:c.670_705+64dup
XM_006722004.2:c.319_354+64dup
XM_006722005.2:c.319_354+64dup
XM_011525092.1:c.319_354+64dup
XM_011525093.1:c.319_354+64dup
XM_011525094.1:c.319_354+64dup
XR_934513.1:n.743_778+64dup
XR_934514.1:n.743_778+64dup
XM_006722001.4:c.670_705+64dup
XM_006722002.4:c.670_705+64dup
XM_006722004.3:c.319_354+64dup
XM_006722005.3:c.319_354+64dup
XM_011525092.2:c.319_354+64dup
XM_011525093.2:c.319_354+64dup
XM_011525094.2:c.319_354+64dup
XM_017024914.1:c.319_354+64dup
XM_017024915.1:c.319_354+64dup
XM_017024916.1:c.319_354+64dup
XM_017024917.1:c.319_354+64dup
XM_017024918.2:c.319_354+64dup
XM_017024919.1:c.319_354+64dup
XR_934513.3:n.1174_1209+64dup
XR_934514.3:n.1174_1209+64dup
NM_058216.3:c.670_705+64dup
NR_103872.2:n.545_580+64dup