Canonical Allele Identifier: CA6270001
Gene: RDX HGNC NCBI

Linked Data

ClinVar Variation Id: 501592
dbSNP Id: rs142161673

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.110233486A>G , CM000673.2:g.110233486A>G GRCh38
NC_000011.9:g.110104211A>G , CM000673.1:g.110104211A>G GRCh37
NC_000011.8:g.109609421A>G NCBI36
NG_023044.1:g.68227T>C
NG_023044.2:g.68227T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000645495.2:c.1345-7T>C MANE Select ENSP00000496503.2:n.1345-7T>C
ENST00000645527.1:c.1345-7T>C ENSP00000496121.1:n.1345-7T>C
ENST00000646663.1:c.1345-7T>C ENSP00000494693.1:n.1345-7T>C
ENST00000647231.1:c.1345-7T>C ENSP00000496414.1:n.1345-7T>C
ENST00000343115.8:c.1345-7T>C ENSP00000342830.4:n.1345-7T>C
ENST00000405097.5:c.1345-7T>C ENSP00000384136.1:n.1345-7T>C
ENST00000527537.5:n.574-7T>C
ENST00000528498.5:c.1345-7T>C ENSP00000432112.1:n.1345-7T>C
ENST00000528900.5:c.304-7T>C ENSP00000433580.1:n.304-7T>C
ENST00000530085.2:n.355-7T>C
ENST00000530131.5:c.*815-7T>C ENSP00000432829.1:n.*815-7T>C
ENST00000530301.5:c.405-1482T>C ENSP00000436277.1:n.405-1482T>C
ENST00000530749.5:c.1345-7T>C ENSP00000437301.1:n.1345-7T>C
ENST00000532461.5:n.460-7T>C
ENST00000533961.1:n.38T>C
ENST00000544551.5:c.937-7T>C ENSP00000445826.1:n.937-7T>C
NM_001260492.1:c.1345-7T>C NP_001247421.1:n.1345-7T>C
NM_001260493.1:c.1345-7T>C NP_001247422.1:n.1345-7T>C
NM_001260494.1:c.937-7T>C NP_001247423.1:n.937-7T>C
NM_001260495.1:c.304-7T>C NP_001247424.1:n.304-7T>C
NM_001260496.1:c.405-1482T>C NP_001247425.1:n.405-1482T>C
NM_002906.3:c.1345-7T>C NP_002897.1:n.1345-7T>C
NM_001260492.2:c.1345-7T>C NP_001247421.1:n.1345-7T>C
NM_002906.4:c.1345-7T>C MANE Select NP_002897.1:n.1345-7T>C
NM_001260493.2:c.1345-7T>C NP_001247422.1:n.1345-7T>C
NM_001260494.2:c.937-7T>C NP_001247423.1:n.937-7T>C
NM_001260495.2:c.304-7T>C NP_001247424.1:n.304-7T>C
NM_001260496.2:c.405-1482T>C NP_001247425.1:n.405-1482T>C