Canonical Allele Identifier: CA10637125
Gene: RDX HGNC NCBI

Linked Data

ClinVar Variation Id: 302358
ClinVar RCV Id: RCV000368258
dbSNP Id: rs78818014

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.110296507G>A , CM000673.2:g.110296507G>A GRCh38
NC_000011.9:g.110167232G>A , CM000673.1:g.110167232G>A GRCh37
NC_000011.8:g.109672442G>A NCBI36
NG_023044.1:g.5206C>T
NG_023044.2:g.5206C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000645495.2:c.-105C>T MANE Select ENSP00000496503.2:n.-105C>T
ENST00000645527.1:c.-313C>T ENSP00000496121.1:n.-313C>T
ENST00000647231.1:c.-105C>T ENSP00000496414.1:n.-105C>T
ENST00000343115.8:c.-105C>T ENSP00000342830.4:n.-105C>T
ENST00000405097.5:c.-105C>T ENSP00000384136.1:n.-105C>T
ENST00000528498.5:c.-105C>T ENSP00000432112.1:n.-105C>T
ENST00000528556.5:c.-105C>T ENSP00000434881.1:n.-105C>T
ENST00000528900.5:c.-199C>T ENSP00000433580.1:n.-199C>T
ENST00000530131.5:c.-105C>T ENSP00000432829.1:n.-105C>T
ENST00000530301.5:c.-105C>T ENSP00000436277.1:n.-105C>T
ENST00000530749.5:c.-105C>T ENSP00000437301.1:n.-105C>T
ENST00000533678.1:c.-105C>T ENSP00000435930.1:n.-105C>T
ENST00000533991.1:c.-62C>T ENSP00000432572.1:n.-62C>T
ENST00000534683.1:c.-222C>T ENSP00000431560.1:n.-222C>T
ENST00000544551.5:c.-142C>T ENSP00000445826.1:n.-142C>T
NM_001260492.1:c.-105C>T NP_001247421.1:n.-105C>T
NM_001260493.1:c.-105C>T NP_001247422.1:n.-105C>T
NM_001260494.1:c.-142C>T NP_001247423.1:n.-142C>T
NM_001260495.1:c.-199C>T NP_001247424.1:n.-199C>T
NM_001260496.1:c.-105C>T NP_001247425.1:n.-105C>T
NM_002906.3:c.-105C>T NP_002897.1:n.-105C>T
NM_001260492.2:c.-105C>T NP_001247421.1:n.-105C>T
NM_002906.4:c.-105C>T MANE Select NP_002897.1:n.-105C>T
NM_001260493.2:c.-105C>T NP_001247422.1:n.-105C>T
NM_001260494.2:c.-142C>T NP_001247423.1:n.-142C>T
NM_001260495.2:c.-199C>T NP_001247424.1:n.-199C>T
NM_001260496.2:c.-105C>T NP_001247425.1:n.-105C>T