Canonical Allele Identifier: CA6270205

Gene: RDX

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.110254118A>G , CM000673.2:g.110254118A>G	GRCh38
NC_000011.9:g.110124843A>G , CM000673.1:g.110124843A>G	GRCh37
NC_000011.8:g.109630053A>G	NCBI36
NG_023044.1:g.47595T>C
NG_023044.2:g.47595T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_002906.4:c.796-9T>C MANE Select	NP_002897.1:n.796-9T>C
ENST00000645495.2:c.796-9T>C MANE Select	ENSP00000496503.2:n.796-9T>C
NM_001260492.1:c.796-9T>C	NP_001247421.1:n.796-9T>C
NM_001260492.2:c.796-9T>C	NP_001247421.1:n.796-9T>C
NM_001260493.1:c.796-9T>C	NP_001247422.1:n.796-9T>C
NM_001260493.2:c.796-9T>C	NP_001247422.1:n.796-9T>C
NM_001260494.1:c.388-9T>C	NP_001247423.1:n.388-9T>C
NM_001260494.2:c.388-9T>C	NP_001247423.1:n.388-9T>C
NM_001260495.1:c.-82-6285T>C	NP_001247424.1:n.-82-6285T>C
NM_001260495.2:c.-82-6285T>C	NP_001247424.1:n.-82-6285T>C
NM_001260496.1:c.404+4039T>C	NP_001247425.1:n.404+4039T>C
NM_001260496.2:c.404+4039T>C	NP_001247425.1:n.404+4039T>C
NM_002906.3:c.796-9T>C	NP_002897.1:n.796-9T>C
ENST00000343115.8:c.796-9T>C	ENSP00000342830.4:n.796-9T>C
ENST00000405097.5:c.796-9T>C	ENSP00000384136.1:n.796-9T>C
ENST00000528498.5:c.796-9T>C	ENSP00000432112.1:n.796-9T>C
ENST00000528900.5:c.-82-6285T>C	ENSP00000433580.1:n.-82-6285T>C
ENST00000529774.1:n.348-9T>C
ENST00000530131.5:c.*266-9T>C	ENSP00000432829.1:n.*266-9T>C
ENST00000530301.5:c.404+4039T>C	ENSP00000436277.1:n.404+4039T>C
ENST00000530749.5:c.796-9T>C	ENSP00000437301.1:n.796-9T>C
ENST00000544551.5:c.388-9T>C	ENSP00000445826.1:n.388-9T>C
ENST00000645527.1:c.796-9T>C	ENSP00000496121.1:n.796-9T>C
ENST00000646663.1:c.796-9T>C	ENSP00000494693.1:n.796-9T>C
ENST00000647231.1:c.796-9T>C	ENSP00000496414.1:n.796-9T>C