Canonical Allele Identifier: CA382868342
Gene: RDX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.110258184A>T , CM000673.2:g.110258184A>T GRCh38
NC_000011.9:g.110128909A>T , CM000673.1:g.110128909A>T GRCh37
NC_000011.8:g.109634119A>T NCBI36
NG_023044.1:g.43529T>A
NG_023044.2:g.43529T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000642511.1:c.431T>A
ENST00000645495.2:c.473T>A MANE Select ENSP00000496503.2:p.Leu158Ter
ENST00000645527.1:c.473T>A ENSP00000496121.1:p.Leu158Ter
ENST00000646663.1:c.473T>A ENSP00000494693.1:p.Leu158Ter
ENST00000647231.1:c.473T>A ENSP00000496414.1:p.Leu158Ter
ENST00000343115.8:c.473T>A ENSP00000342830.4:p.Leu158Ter
ENST00000405097.5:c.473T>A ENSP00000384136.1:p.Leu158Ter
ENST00000528498.5:c.473T>A ENSP00000432112.1:p.Leu158Ter
ENST00000528900.5:c.-82-10351T>A ENSP00000433580.1:n.-82-10351T>A
ENST00000529774.1:n.25T>A
ENST00000530131.5:c.102T>A ENSP00000432829.1:p.Ile34=
ENST00000530301.5:c.377T>A ENSP00000436277.1:p.Leu126Ter
ENST00000530749.5:c.473T>A ENSP00000437301.1:p.Leu158Ter
ENST00000532118.5:c.440T>A ENSP00000437140.1:p.Leu147Ter
ENST00000534683.1:c.-71T>A ENSP00000431560.1:n.-71T>A
ENST00000544551.5:c.65T>A ENSP00000445826.1:p.Leu22Ter
NM_001260492.1:c.473T>A NP_001247421.1:p.Leu158Ter
NM_001260493.1:c.473T>A NP_001247422.1:p.Leu158Ter
NM_001260494.1:c.65T>A NP_001247423.1:p.Leu22Ter
NM_001260495.1:c.-82-10351T>A NP_001247424.1:n.-82-10351T>A
NM_001260496.1:c.377T>A NP_001247425.1:p.Leu126Ter
NM_002906.3:c.473T>A NP_002897.1:p.Leu158Ter
NM_001260492.2:c.473T>A NP_001247421.1:p.Leu158Ter
NM_002906.4:c.473T>A MANE Select NP_002897.1:p.Leu158Ter
NM_001260493.2:c.473T>A NP_001247422.1:p.Leu158Ter
NM_001260494.2:c.65T>A NP_001247423.1:p.Leu22Ter
NM_001260495.2:c.-82-10351T>A NP_001247424.1:n.-82-10351T>A
NM_001260496.2:c.377T>A NP_001247425.1:p.Leu126Ter