Canonical Allele Identifier: CA10633381

Gene: RDX

Linked Data

• ClinVar Variation Id: 302340
• ClinVar RCV Id: RCV000363910
• dbSNP Id: rs186249296
• gnomAD v2: 11-110102438-T-C
• gnomAD v3: 11-110231713-T-C
• gnomAD v4: 11-110231713-T-C
• MyVariant Identifiers: chr11:g.110102438T>C (hg19) ; chr11:g.110231713T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.110231713T>C , CM000673.2:g.110231713T>C	GRCh38
NC_000011.9:g.110102438T>C , CM000673.1:g.110102438T>C	GRCh37
NC_000011.8:g.109607648T>C	NCBI36
NG_023044.1:g.70000A>G
NG_023044.2:g.70000A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645312.1:c.391+160A>G
ENST00000645495.2:c.*156A>G MANE Select	ENSP00000496503.2:n.*156A>G
ENST00000645527.1:c.1587+1524A>G	ENSP00000496121.1:n.1587+1524A>G
ENST00000646663.1:c.1748+160A>G	ENSP00000494693.1:n.1748+160A>G
ENST00000647231.1:c.1748+160A>G	ENSP00000496414.1:n.1748+160A>G
ENST00000343115.8:c.*156A>G	ENSP00000342830.4:n.*156A>G
ENST00000405097.5:c.1748+160A>G	ENSP00000384136.1:n.1748+160A>G
ENST00000527537.5:n.1137A>G
ENST00000528498.5:c.1748+160A>G	ENSP00000432112.1:n.1748+160A>G
ENST00000528900.5:c.707+160A>G	ENSP00000433580.1:n.707+160A>G
ENST00000530131.5:c.*1378A>G	ENSP00000432829.1:n.*1378A>G
ENST00000530301.5:c.536+160A>G	ENSP00000436277.1:n.536+160A>G
ENST00000530749.5:c.1748+160A>G	ENSP00000437301.1:n.1748+160A>G
ENST00000532461.5:n.1023A>G
ENST00000533961.1:n.608A>G
ENST00000544551.5:c.*156A>G	ENSP00000445826.1:n.*156A>G
NM_001260492.1:c.1748+160A>G	NP_001247421.1:n.1748+160A>G
NM_001260493.1:c.1748+160A>G	NP_001247422.1:n.1748+160A>G
NM_001260494.1:c.*156A>G	NP_001247423.1:n.*156A>G
NM_001260495.1:c.707+160A>G	NP_001247424.1:n.707+160A>G
NM_001260496.1:c.536+160A>G	NP_001247425.1:n.536+160A>G
NM_002906.3:c.*156A>G	NP_002897.1:n.*156A>G
NM_001260492.2:c.1748+160A>G	NP_001247421.1:n.1748+160A>G
NM_002906.4:c.*156A>G MANE Select	NP_002897.1:n.*156A>G
NM_001260493.2:c.1748+160A>G	NP_001247422.1:n.1748+160A>G
NM_001260494.2:c.*156A>G	NP_001247423.1:n.*156A>G
NM_001260495.2:c.707+160A>G	NP_001247424.1:n.707+160A>G
NM_001260496.2:c.536+160A>G	NP_001247425.1:n.536+160A>G