Canonical Allele Identifier: CA382868175
Gene: RDX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.110258116C>G , CM000673.2:g.110258116C>G GRCh38
NC_000011.9:g.110128841C>G , CM000673.1:g.110128841C>G GRCh37
NC_000011.8:g.109634051C>G NCBI36
NG_023044.1:g.43597G>C
NG_023044.2:g.43597G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000642511.1:c.499G>C
ENST00000645495.2:c.541G>C MANE Select ENSP00000496503.2:p.Gly181Arg
ENST00000645527.1:c.541G>C ENSP00000496121.1:p.Gly181Arg
ENST00000646663.1:c.541G>C ENSP00000494693.1:p.Gly181Arg
ENST00000647231.1:c.541G>C ENSP00000496414.1:p.Gly181Arg
ENST00000343115.8:c.541G>C ENSP00000342830.4:p.Gly181Arg
ENST00000405097.5:c.541G>C ENSP00000384136.1:p.Gly181Arg
ENST00000528498.5:c.541G>C ENSP00000432112.1:p.Gly181Arg
ENST00000528900.5:c.-82-10283G>C ENSP00000433580.1:n.-82-10283G>C
ENST00000529774.1:n.93G>C
ENST00000530131.5:c.*11G>C ENSP00000432829.1:n.*11G>C
ENST00000530301.5:c.404+41G>C ENSP00000436277.1:n.404+41G>C
ENST00000530749.5:c.541G>C ENSP00000437301.1:p.Gly181Arg
ENST00000534683.1:c.-3G>C ENSP00000431560.1:n.-3G>C
ENST00000544551.5:c.133G>C ENSP00000445826.1:p.Gly45Arg
NM_001260492.1:c.541G>C NP_001247421.1:p.Gly181Arg
NM_001260493.1:c.541G>C NP_001247422.1:p.Gly181Arg
NM_001260494.1:c.133G>C NP_001247423.1:p.Gly45Arg
NM_001260495.1:c.-82-10283G>C NP_001247424.1:n.-82-10283G>C
NM_001260496.1:c.404+41G>C NP_001247425.1:n.404+41G>C
NM_002906.3:c.541G>C NP_002897.1:p.Gly181Arg
NM_001260492.2:c.541G>C NP_001247421.1:p.Gly181Arg
NM_002906.4:c.541G>C MANE Select NP_002897.1:p.Gly181Arg
NM_001260493.2:c.541G>C NP_001247422.1:p.Gly181Arg
NM_001260494.2:c.133G>C NP_001247423.1:p.Gly45Arg
NM_001260495.2:c.-82-10283G>C NP_001247424.1:n.-82-10283G>C
NM_001260496.2:c.404+41G>C NP_001247425.1:n.404+41G>C