Canonical Allele Identifier: CA6270284
Gene: RDX HGNC NCBI

Linked Data

dbSNP Id: rs769507937

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.110258075A>G , CM000673.2:g.110258075A>G GRCh38
NC_000011.9:g.110128800A>G , CM000673.1:g.110128800A>G GRCh37
NC_000011.8:g.109634010A>G NCBI36
NG_023044.1:g.43638T>C
NG_023044.2:g.43638T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000645495.2:c.551+31T>C MANE Select ENSP00000496503.2:n.551+31T>C
ENST00000645527.1:c.551+31T>C ENSP00000496121.1:n.551+31T>C
ENST00000646663.1:c.551+31T>C ENSP00000494693.1:n.551+31T>C
ENST00000647231.1:c.551+31T>C ENSP00000496414.1:n.551+31T>C
ENST00000343115.8:c.551+31T>C ENSP00000342830.4:n.551+31T>C
ENST00000405097.5:c.551+31T>C ENSP00000384136.1:n.551+31T>C
ENST00000528498.5:c.551+31T>C ENSP00000432112.1:n.551+31T>C
ENST00000528900.5:c.-82-10242T>C ENSP00000433580.1:n.-82-10242T>C
ENST00000529774.1:n.103+31T>C
ENST00000530131.5:c.*21+31T>C ENSP00000432829.1:n.*21+31T>C
ENST00000530301.5:c.404+82T>C ENSP00000436277.1:n.404+82T>C
ENST00000530749.5:c.551+31T>C ENSP00000437301.1:n.551+31T>C
ENST00000534683.1:c.8+31T>C ENSP00000431560.1:n.8+31T>C
ENST00000544551.5:c.143+31T>C ENSP00000445826.1:n.143+31T>C
NM_001260492.1:c.551+31T>C NP_001247421.1:n.551+31T>C
NM_001260493.1:c.551+31T>C NP_001247422.1:n.551+31T>C
NM_001260494.1:c.143+31T>C NP_001247423.1:n.143+31T>C
NM_001260495.1:c.-82-10242T>C NP_001247424.1:n.-82-10242T>C
NM_001260496.1:c.404+82T>C NP_001247425.1:n.404+82T>C
NM_002906.3:c.551+31T>C NP_002897.1:n.551+31T>C
NM_001260492.2:c.551+31T>C NP_001247421.1:n.551+31T>C
NM_002906.4:c.551+31T>C MANE Select NP_002897.1:n.551+31T>C
NM_001260493.2:c.551+31T>C NP_001247422.1:n.551+31T>C
NM_001260494.2:c.143+31T>C NP_001247423.1:n.143+31T>C
NM_001260495.2:c.-82-10242T>C NP_001247424.1:n.-82-10242T>C
NM_001260496.2:c.404+82T>C NP_001247425.1:n.404+82T>C