Canonical Allele Identifier: CA476752001

Gene: RDX

Linked Data

• MyVariant Identifiers: chr11:g.110102618A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.110231893A>C , CM000673.2:g.110231893A>C	GRCh38
NC_000011.9:g.110102618A>C , CM000673.1:g.110102618A>C	GRCh37
NC_000011.8:g.109607828A>C	NCBI36
NG_023044.1:g.69820T>G
NG_023044.2:g.69820T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000645312.1:c.371T>G
ENST00000645495.2:c.1728T>G MANE Select	ENSP00000496503.2:p.Arg576=
ENST00000645527.1:c.1587+1344T>G	ENSP00000496121.1:n.1587+1344T>G
ENST00000646663.1:c.1728T>G	ENSP00000494693.1:p.Arg576=
ENST00000647231.1:c.1728T>G	ENSP00000496414.1:p.Arg576=
ENST00000343115.8:c.1728T>G	ENSP00000342830.4:p.Arg576=
ENST00000405097.5:c.1728T>G	ENSP00000384136.1:p.Arg576=
ENST00000527537.5:n.957T>G
ENST00000528498.5:c.1728T>G	ENSP00000432112.1:p.Arg576=
ENST00000528900.5:c.687T>G	ENSP00000433580.1:p.Arg229=
ENST00000530085.2:n.738T>G
ENST00000530131.5:c.*1198T>G	ENSP00000432829.1:n.*1198T>G
ENST00000530301.5:c.516T>G	ENSP00000436277.1:p.Arg172=
ENST00000530749.5:c.1728T>G	ENSP00000437301.1:p.Arg576=
ENST00000532461.5:n.843T>G
ENST00000533961.1:n.428T>G
ENST00000544551.5:c.1320T>G	ENSP00000445826.1:p.Arg440=
NM_001260492.1:c.1728T>G	NP_001247421.1:p.Arg576=
NM_001260493.1:c.1728T>G	NP_001247422.1:p.Arg576=
NM_001260494.1:c.1320T>G	NP_001247423.1:p.Arg440=
NM_001260495.1:c.687T>G	NP_001247424.1:p.Arg229=
NM_001260496.1:c.516T>G	NP_001247425.1:p.Arg172=
NM_002906.3:c.1728T>G	NP_002897.1:p.Arg576=
NM_001260492.2:c.1728T>G	NP_001247421.1:p.Arg576=
NM_002906.4:c.1728T>G MANE Select	NP_002897.1:p.Arg576=
NM_001260493.2:c.1728T>G	NP_001247422.1:p.Arg576=
NM_001260494.2:c.1320T>G	NP_001247423.1:p.Arg440=
NM_001260495.2:c.687T>G	NP_001247424.1:p.Arg229=
NM_001260496.2:c.516T>G	NP_001247425.1:p.Arg172=