Canonical Allele Identifier: CA382570542
Gene: RDX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.110231900T>A , CM000673.2:g.110231900T>A GRCh38
NC_000011.9:g.110102625T>A , CM000673.1:g.110102625T>A GRCh37
NC_000011.8:g.109607835T>A NCBI36
NG_023044.1:g.69813A>T
NG_023044.2:g.69813A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000645312.1:c.364A>T
ENST00000645495.2:c.1721A>T MANE Select ENSP00000496503.2:p.Lys574Met
ENST00000645527.1:c.1587+1337A>T ENSP00000496121.1:n.1587+1337A>T
ENST00000646663.1:c.1721A>T ENSP00000494693.1:p.Lys574Met
ENST00000647231.1:c.1721A>T ENSP00000496414.1:p.Lys574Met
ENST00000343115.8:c.1721A>T ENSP00000342830.4:p.Lys574Met
ENST00000405097.5:c.1721A>T ENSP00000384136.1:p.Lys574Met
ENST00000527537.5:n.950A>T
ENST00000528498.5:c.1721A>T ENSP00000432112.1:p.Lys574Met
ENST00000528900.5:c.680A>T ENSP00000433580.1:p.Lys227Met
ENST00000530085.2:n.731A>T
ENST00000530131.5:c.*1191A>T ENSP00000432829.1:n.*1191A>T
ENST00000530301.5:c.509A>T ENSP00000436277.1:p.Lys170Met
ENST00000530749.5:c.1721A>T ENSP00000437301.1:p.Lys574Met
ENST00000532461.5:n.836A>T
ENST00000533961.1:n.421A>T
ENST00000544551.5:c.1313A>T ENSP00000445826.1:p.Lys438Met
NM_001260492.1:c.1721A>T NP_001247421.1:p.Lys574Met
NM_001260493.1:c.1721A>T NP_001247422.1:p.Lys574Met
NM_001260494.1:c.1313A>T NP_001247423.1:p.Lys438Met
NM_001260495.1:c.680A>T NP_001247424.1:p.Lys227Met
NM_001260496.1:c.509A>T NP_001247425.1:p.Lys170Met
NM_002906.3:c.1721A>T NP_002897.1:p.Lys574Met
NM_001260492.2:c.1721A>T NP_001247421.1:p.Lys574Met
NM_002906.4:c.1721A>T MANE Select NP_002897.1:p.Lys574Met
NM_001260493.2:c.1721A>T NP_001247422.1:p.Lys574Met
NM_001260494.2:c.1313A>T NP_001247423.1:p.Lys438Met
NM_001260495.2:c.680A>T NP_001247424.1:p.Lys227Met
NM_001260496.2:c.509A>T NP_001247425.1:p.Lys170Met