Canonical Allele Identifier: CA14177077
Gene: RAD51 HGNC NCBI
MyVariant.info:
GRCh38 chr15:g.40729082C>G
GRCh37 chr15:g.41021280C>G
gnomAD v2:
15:41021280 C / G
gnomAD v3:
15:40729082 C / G
gnomAD v4:
chr15-40729082-C-G
Joint Max Group AF 0.6526047 (EAS)
Genomes Max Group AF 0.6526047 (EAS)
ClinVar RCV:
RCV001538782
ClinVar Variation:
1181406
dbSNP:
4417527
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40729082C>G , CM000677.2:g.40729082C>G GRCh38
NC_000015.9:g.41021280C>G , CM000677.1:g.41021280C>G GRCh37
NC_000015.8:g.38808572C>G NCBI36
NG_012120.1:g.38922C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000267868.8:c.644+258C>G MANE Select ENSP00000267868.3:n.644+258C>G
ENST00000532743.6:c.644+258C>G ENSP00000433924.2:n.644+258C>G
ENST00000645673.2:c.647+258C>G ENSP00000493712.2:n.647+258C>G
ENST00000267868.7:c.644+258C>G ENSP00000267868.3:n.644+258C>G
ENST00000382643.7:c.647+258C>G ENSP00000372088.3:n.647+258C>G
ENST00000423169.6:c.644+258C>G ENSP00000406602.2:n.644+258C>G
ENST00000525066.5:c.*93+258C>G ENSP00000431864.1:n.*93+258C>G
ENST00000531277.2:c.*223+258C>G ENSP00000436512.2:n.*223+258C>G
ENST00000532743.5:c.647+258C>G ENSP00000433924.1:n.647+258C>G
ENST00000557850.5:c.353+258C>G ENSP00000454176.1:n.353+258C>G
NM_001164269.1:c.647+258C>G NP_001157741.1:n.647+258C>G
NM_001164270.1:c.644+258C>G NP_001157742.1:n.644+258C>G
NM_002875.4:c.644+258C>G NP_002866.2:n.644+258C>G
NM_133487.3:c.647+258C>G NP_597994.3:n.647+258C>G
XM_006720626.2:c.644+258C>G XP_006720689.1:n.644+258C>G
XM_011521857.1:c.644+258C>G XP_011520159.1:n.644+258C>G
XM_011521858.1:c.644+258C>G XP_011520160.1:n.644+258C>G
XM_011521859.1:c.644+258C>G XP_011520161.1:n.644+258C>G
XM_011521860.1:c.644+258C>G XP_011520162.1:n.644+258C>G
XM_011521861.1:c.644+258C>G XP_011520163.1:n.644+258C>G
XM_011521862.1:c.272+258C>G XP_011520164.1:n.272+258C>G
XM_006720626.3:c.644+258C>G XP_006720689.1:n.644+258C>G
XM_011521857.2:c.644+258C>G XP_011520159.1:n.644+258C>G
XM_011521858.2:c.644+258C>G XP_011520160.1:n.644+258C>G
XM_011521859.2:c.644+258C>G XP_011520161.1:n.644+258C>G
XM_011521860.2:c.644+258C>G XP_011520162.1:n.644+258C>G
XM_011521861.2:c.644+258C>G XP_011520163.1:n.644+258C>G
XM_011521862.3:c.272+258C>G XP_011520164.1:n.272+258C>G
NM_001164269.2:c.647+258C>G NP_001157741.1:n.647+258C>G
NM_001164270.2:c.644+258C>G NP_001157742.1:n.644+258C>G
NM_002875.5:c.644+258C>G MANE Select NP_002866.2:n.644+258C>G
NM_133487.4:c.647+258C>G NP_597994.3:n.647+258C>G
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