Canonical Allele Identifier: CA382868292
Gene: RDX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.110258162T>G , CM000673.2:g.110258162T>G GRCh38
NC_000011.9:g.110128887T>G , CM000673.1:g.110128887T>G GRCh37
NC_000011.8:g.109634097T>G NCBI36
NG_023044.1:g.43551A>C
NG_023044.2:g.43551A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000642511.1:c.453A>C
ENST00000645495.2:c.495A>C MANE Select ENSP00000496503.2:p.Lys165Asn
ENST00000645527.1:c.495A>C ENSP00000496121.1:p.Lys165Asn
ENST00000646663.1:c.495A>C ENSP00000494693.1:p.Lys165Asn
ENST00000647231.1:c.495A>C ENSP00000496414.1:p.Lys165Asn
ENST00000343115.8:c.495A>C ENSP00000342830.4:p.Lys165Asn
ENST00000405097.5:c.495A>C ENSP00000384136.1:p.Lys165Asn
ENST00000528498.5:c.495A>C ENSP00000432112.1:p.Lys165Asn
ENST00000528900.5:c.-82-10329A>C ENSP00000433580.1:n.-82-10329A>C
ENST00000529774.1:n.47A>C
ENST00000530131.5:c.124A>C ENSP00000432829.1:p.Arg42=
ENST00000530301.5:c.399A>C ENSP00000436277.1:p.Lys133Asn
ENST00000530749.5:c.495A>C ENSP00000437301.1:p.Lys165Asn
ENST00000534683.1:c.-49A>C ENSP00000431560.1:n.-49A>C
ENST00000544551.5:c.87A>C ENSP00000445826.1:p.Lys29Asn
NM_001260492.1:c.495A>C NP_001247421.1:p.Lys165Asn
NM_001260493.1:c.495A>C NP_001247422.1:p.Lys165Asn
NM_001260494.1:c.87A>C NP_001247423.1:p.Lys29Asn
NM_001260495.1:c.-82-10329A>C NP_001247424.1:n.-82-10329A>C
NM_001260496.1:c.399A>C NP_001247425.1:p.Lys133Asn
NM_002906.3:c.495A>C NP_002897.1:p.Lys165Asn
NM_001260492.2:c.495A>C NP_001247421.1:p.Lys165Asn
NM_002906.4:c.495A>C MANE Select NP_002897.1:p.Lys165Asn
NM_001260493.2:c.495A>C NP_001247422.1:p.Lys165Asn
NM_001260494.2:c.87A>C NP_001247423.1:p.Lys29Asn
NM_001260495.2:c.-82-10329A>C NP_001247424.1:n.-82-10329A>C
NM_001260496.2:c.399A>C NP_001247425.1:p.Lys133Asn