Canonical Allele Identifier: CA228497421

Gene: RDX

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.110235877T>C , CM000673.2:g.110235877T>C	GRCh38
NC_000011.9:g.110106602T>C , CM000673.1:g.110106602T>C	GRCh37
NC_000011.8:g.109611812T>C	NCBI36
NG_023044.1:g.65836A>G
NG_023044.2:g.65836A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002906.4:c.1344+222A>G MANE Select	NP_002897.1:n.1344+222A>G
ENST00000645495.2:c.1344+222A>G MANE Select	ENSP00000496503.2:n.1344+222A>G
NM_001260492.1:c.1344+222A>G	NP_001247421.1:n.1344+222A>G
NM_001260492.2:c.1344+222A>G	NP_001247421.1:n.1344+222A>G
NM_001260493.1:c.1344+222A>G	NP_001247422.1:n.1344+222A>G
NM_001260493.2:c.1344+222A>G	NP_001247422.1:n.1344+222A>G
NM_001260494.1:c.936+222A>G	NP_001247423.1:n.936+222A>G
NM_001260494.2:c.936+222A>G	NP_001247423.1:n.936+222A>G
NM_001260495.1:c.303+222A>G	NP_001247424.1:n.303+222A>G
NM_001260495.2:c.303+222A>G	NP_001247424.1:n.303+222A>G
NM_001260496.1:c.405-3873A>G	NP_001247425.1:n.405-3873A>G
NM_001260496.2:c.405-3873A>G	NP_001247425.1:n.405-3873A>G
NM_002906.3:c.1344+222A>G	NP_002897.1:n.1344+222A>G
ENST00000343115.8:c.1344+222A>G	ENSP00000342830.4:n.1344+222A>G
ENST00000405097.5:c.1344+222A>G	ENSP00000384136.1:n.1344+222A>G
ENST00000527537.5:n.573+222A>G
ENST00000528498.5:c.1344+222A>G	ENSP00000432112.1:n.1344+222A>G
ENST00000528900.5:c.303+222A>G	ENSP00000433580.1:n.303+222A>G
ENST00000530085.2:n.354+222A>G
ENST00000530131.5:c.*814+222A>G	ENSP00000432829.1:n.*814+222A>G
ENST00000530301.5:c.405-3873A>G	ENSP00000436277.1:n.405-3873A>G
ENST00000530749.5:c.1344+222A>G	ENSP00000437301.1:n.1344+222A>G
ENST00000532461.5:n.459+222A>G
ENST00000544551.5:c.936+222A>G	ENSP00000445826.1:n.936+222A>G
ENST00000645527.1:c.1344+222A>G	ENSP00000496121.1:n.1344+222A>G
ENST00000646663.1:c.1344+222A>G	ENSP00000494693.1:n.1344+222A>G
ENST00000647231.1:c.1344+222A>G	ENSP00000496414.1:n.1344+222A>G