Canonical Allele Identifier: CA10580746

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 232156
• ClinVar RCV Id: RCV000216680 ; RCV000532240 ; RCV001535621
• dbSNP Id: rs1555597214
• gnomAD v2: 17-56780655-T-TATCTTCTTCCAGATTTCCTTTCAGAACACTCAAAGGTATGAGTCAGACTACTGAAATGTAACTAACCAAGTATTTTTTGAGGTGTTTGATAAGCATGAA
• gnomAD v3: 17-58703294-T-TATCTTCTTCCAGATTTCCTTTCAGAACACTCAAAGGTATGAGTCAGACTACTGAAATGTAACTAACCAAGTATTTTTTGAGGTGTTTGATAAGCATGAA
• gnomAD v4: 17-58703294-T-TATCTTCTTCCAGATTTCCTTTCAGAACACTCAAAGGTATGAGTCAGACTACTGAAATGTAACTAACCAAGTATTTTTTGAGGTGTTTGATAAGCATGAA
• MyVariant Identifiers: chr17:g.56780657_56780755dup (hg19) ; chr17:g.56780657_56780755dup99 (hg19) ; chr17:g.56780655_56780656insATCTTCTTCCAGATTTCCTTTCAGAACACTCAAAGGTATGAGTCAGACTACTGAAATGTAACTAACCAAGTATTTTTTGAGGTGTTTGATAAGCATGAA (hg19) ; chr17:g.58703296_58703394dup (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703296_58703394dup , CM000679.2:g.58703296_58703394dup	GRCh38
NC_000017.10:g.56780657_56780755dup , CM000679.1:g.56780657_56780755dup	GRCh37
NC_000017.9:g.54135656_54135754dup	NCBI36
NG_023199.1:g.15695_15793dup , LRG_314:g.15695_15793dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.321_354+65dup
ENST00000697677.1:n.1753_1851dup
ENST00000697678.1:n.574_607+65dup
ENST00000697679.1:n.1746_1779+65dup
ENST00000697680.1:c.*1536_*1569+65dup
ENST00000697681.1:c.*1688_*1721+65dup
ENST00000697683.1:c.*1536_*1569+65dup
ENST00000697684.1:n.732_765+65dup
ENST00000697685.1:c.*1369_*1402+65dup
ENST00000697686.1:c.321_354+65dup
ENST00000697687.1:n.551_584+65dup
ENST00000697688.1:n.718_751+65dup
ENST00000697689.1:c.*1208_*1241+65dup
ENST00000697690.1:c.672_705+65dup
ENST00000697691.1:c.*644_*677+65dup
ENST00000697692.1:c.*684_*717+65dup
ENST00000697694.1:c.321_354+65dup
ENST00000697695.1:n.1279_1312+65dup
ENST00000337432.9:c.672_705+65dup
ENST00000337432.8:c.672_705+65dup
ENST00000413590.5:c.310_343+65dup
ENST00000425173.5:c.468_501+65dup
ENST00000461271.5:c.321_354+65dup
ENST00000475762.5:c.*1375_*1408+65dup
ENST00000482007.5:c.*100_*133+65dup
ENST00000487525.5:c.*100_*133+65dup
ENST00000487921.5:n.584_617+65dup
ENST00000583539.5:c.672_705+65dup
ENST00000584617.5:c.394_427+65dup
NM_058216.2:c.672_705+65dup
NR_103872.1:n.576_609+65dup
XM_006722001.2:c.672_705+65dup
XM_006722002.2:c.672_705+65dup
XM_006722004.2:c.321_354+65dup
XM_006722005.2:c.321_354+65dup
XM_011525092.1:c.321_354+65dup
XM_011525093.1:c.321_354+65dup
XM_011525094.1:c.321_354+65dup
XR_934513.1:n.745_778+65dup
XR_934514.1:n.745_778+65dup
XM_006722001.4:c.672_705+65dup
XM_006722002.4:c.672_705+65dup
XM_006722004.3:c.321_354+65dup
XM_006722005.3:c.321_354+65dup
XM_011525092.2:c.321_354+65dup
XM_011525093.2:c.321_354+65dup
XM_011525094.2:c.321_354+65dup
XM_017024914.1:c.321_354+65dup
XM_017024915.1:c.321_354+65dup
XM_017024916.1:c.321_354+65dup
XM_017024917.1:c.321_354+65dup
XM_017024918.2:c.321_354+65dup
XM_017024919.1:c.321_354+65dup
XR_934513.3:n.1176_1209+65dup
XR_934514.3:n.1176_1209+65dup
NM_058216.3:c.672_705+65dup
NR_103872.2:n.547_580+65dup