Canonical Allele Identifier: CA1999729332
Gene: RDX HGNC NCBI

Linked Data

dbSNP Id: rs1859910723

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.110263941_110263944dup , CM000673.2:g.110263941_110263944dup GRCh38
NC_000011.9:g.110134666_110134669dup , CM000673.1:g.110134666_110134669dup GRCh37
NC_000011.8:g.109639876_109639879dup NCBI36
NG_023044.1:g.37770_37773dup
NG_023044.2:g.37770_37773dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000642511.1:c.321+17_321+20dup
ENST00000645495.2:c.467+17_467+20dup MANE Select ENSP00000496503.2:n.467+17_467+20dup
ENST00000645527.1:c.467+17_467+20dup ENSP00000496121.1:n.467+17_467+20dup
ENST00000646663.1:c.467+17_467+20dup ENSP00000494693.1:n.467+17_467+20dup
ENST00000647231.1:c.467+17_467+20dup ENSP00000496414.1:n.467+17_467+20dup
ENST00000343115.8:c.467+17_467+20dup ENSP00000342830.4:n.467+17_467+20dup
ENST00000405097.5:c.467+17_467+20dup ENSP00000384136.1:n.467+17_467+20dup
ENST00000528498.5:c.467+17_467+20dup ENSP00000432112.1:n.467+17_467+20dup
ENST00000528900.5:c.-83+15738_-83+15741dup ENSP00000433580.1:n.-83+15738_-83+15741dup
ENST00000530131.5:c.97-5754_97-5751dup ENSP00000432829.1:n.97-5754_97-5751dup
ENST00000530301.5:c.371+17_371+20dup ENSP00000436277.1:n.371+17_371+20dup
ENST00000530749.5:c.467+17_467+20dup ENSP00000437301.1:n.467+17_467+20dup
ENST00000532118.5:c.434+17_434+20dup ENSP00000437140.1:n.434+17_434+20dup
ENST00000534683.1:c.-77+17_-77+20dup ENSP00000431560.1:n.-77+17_-77+20dup
ENST00000544551.5:c.60-5754_60-5751dup ENSP00000445826.1:n.60-5754_60-5751dup
NM_001260492.1:c.467+17_467+20dup NP_001247421.1:n.467+17_467+20dup
NM_001260493.1:c.467+17_467+20dup NP_001247422.1:n.467+17_467+20dup
NM_001260494.1:c.60-5754_60-5751dup NP_001247423.1:n.60-5754_60-5751dup
NM_001260495.1:c.-83+15738_-83+15741dup NP_001247424.1:n.-83+15738_-83+15741dup
NM_001260496.1:c.371+17_371+20dup NP_001247425.1:n.371+17_371+20dup
NM_002906.3:c.467+17_467+20dup NP_002897.1:n.467+17_467+20dup
NM_001260492.2:c.467+17_467+20dup NP_001247421.1:n.467+17_467+20dup
NM_002906.4:c.467+17_467+20dup MANE Select NP_002897.1:n.467+17_467+20dup
NM_001260493.2:c.467+17_467+20dup NP_001247422.1:n.467+17_467+20dup
NM_001260494.2:c.60-5754_60-5751dup NP_001247423.1:n.60-5754_60-5751dup
NM_001260495.2:c.-83+15738_-83+15741dup NP_001247424.1:n.-83+15738_-83+15741dup
NM_001260496.2:c.371+17_371+20dup NP_001247425.1:n.371+17_371+20dup