Canonical Allele Identifier: CA2602627801
Gene: RDX HGNC NCBI

Linked Data

dbSNP Id: rs2134469115

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.110296517G>C , CM000673.2:g.110296517G>C GRCh38
NC_000011.9:g.110167242G>C , CM000673.1:g.110167242G>C GRCh37
NC_000011.8:g.109672452G>C NCBI36
NG_023044.1:g.5196C>G
NG_023044.2:g.5196C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000645495.2:c.-115C>G MANE Select ENSP00000496503.2:n.-115C>G
ENST00000645527.1:c.-323C>G ENSP00000496121.1:n.-323C>G
ENST00000647231.1:c.-115C>G ENSP00000496414.1:n.-115C>G
ENST00000343115.8:c.-115C>G ENSP00000342830.4:n.-115C>G
ENST00000405097.5:c.-115C>G ENSP00000384136.1:n.-115C>G
ENST00000528498.5:c.-115C>G ENSP00000432112.1:n.-115C>G
ENST00000528556.5:c.-115C>G ENSP00000434881.1:n.-115C>G
ENST00000528900.5:c.-209C>G ENSP00000433580.1:n.-209C>G
ENST00000530131.5:c.-115C>G ENSP00000432829.1:n.-115C>G
ENST00000530301.5:c.-115C>G ENSP00000436277.1:n.-115C>G
ENST00000530749.5:c.-115C>G ENSP00000437301.1:n.-115C>G
ENST00000533678.1:c.-115C>G ENSP00000435930.1:n.-115C>G
ENST00000533991.1:c.-72C>G ENSP00000432572.1:n.-72C>G
ENST00000534683.1:c.-232C>G ENSP00000431560.1:n.-232C>G
ENST00000544551.5:c.-152C>G ENSP00000445826.1:n.-152C>G
NM_001260492.1:c.-115C>G NP_001247421.1:n.-115C>G
NM_001260493.1:c.-115C>G NP_001247422.1:n.-115C>G
NM_001260494.1:c.-152C>G NP_001247423.1:n.-152C>G
NM_001260495.1:c.-209C>G NP_001247424.1:n.-209C>G
NM_001260496.1:c.-115C>G NP_001247425.1:n.-115C>G
NM_002906.3:c.-115C>G NP_002897.1:n.-115C>G
NM_001260492.2:c.-115C>G NP_001247421.1:n.-115C>G
NM_002906.4:c.-115C>G MANE Select NP_002897.1:n.-115C>G
NM_001260493.2:c.-115C>G NP_001247422.1:n.-115C>G
NM_001260494.2:c.-152C>G NP_001247423.1:n.-152C>G
NM_001260495.2:c.-209C>G NP_001247424.1:n.-209C>G
NM_001260496.2:c.-115C>G NP_001247425.1:n.-115C>G