Canonical Allele Identifier: CA602139235

Gene: RDX

Linked Data

• ClinVar Variation Id: 2980520
• ClinVar RCV Id: RCV003839678
• dbSNP Id: rs1272952632
• gnomAD v2: 11-110124663-C-A
• gnomAD v4: 11-110253938-C-A
• MyVariant Identifiers: chr11:g.110124663C>A (hg19) ; chr11:g.110253938C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.110253938C>A , CM000673.2:g.110253938C>A	GRCh38
NC_000011.9:g.110124663C>A , CM000673.1:g.110124663C>A	GRCh37
NC_000011.8:g.109629873C>A	NCBI36
NG_023044.1:g.47775G>T
NG_023044.2:g.47775G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645495.2:c.959+8G>T MANE Select	ENSP00000496503.2:n.959+8G>T
ENST00000645527.1:c.959+8G>T	ENSP00000496121.1:n.959+8G>T
ENST00000646663.1:c.959+8G>T	ENSP00000494693.1:n.959+8G>T
ENST00000647231.1:c.959+8G>T	ENSP00000496414.1:n.959+8G>T
ENST00000343115.8:c.959+8G>T	ENSP00000342830.4:n.959+8G>T
ENST00000405097.5:c.959+8G>T	ENSP00000384136.1:n.959+8G>T
ENST00000528498.5:c.959+8G>T	ENSP00000432112.1:n.959+8G>T
ENST00000528900.5:c.-82-6105G>T	ENSP00000433580.1:n.-82-6105G>T
ENST00000530131.5:c.*429+8G>T	ENSP00000432829.1:n.*429+8G>T
ENST00000530301.5:c.404+4219G>T	ENSP00000436277.1:n.404+4219G>T
ENST00000530749.5:c.959+8G>T	ENSP00000437301.1:n.959+8G>T
ENST00000544551.5:c.551+8G>T	ENSP00000445826.1:n.551+8G>T
NM_001260492.1:c.959+8G>T	NP_001247421.1:n.959+8G>T
NM_001260493.1:c.959+8G>T	NP_001247422.1:n.959+8G>T
NM_001260494.1:c.551+8G>T	NP_001247423.1:n.551+8G>T
NM_001260495.1:c.-82-6105G>T	NP_001247424.1:n.-82-6105G>T
NM_001260496.1:c.404+4219G>T	NP_001247425.1:n.404+4219G>T
NM_002906.3:c.959+8G>T	NP_002897.1:n.959+8G>T
NM_001260492.2:c.959+8G>T	NP_001247421.1:n.959+8G>T
NM_002906.4:c.959+8G>T MANE Select	NP_002897.1:n.959+8G>T
NM_001260493.2:c.959+8G>T	NP_001247422.1:n.959+8G>T
NM_001260494.2:c.551+8G>T	NP_001247423.1:n.551+8G>T
NM_001260495.2:c.-82-6105G>T	NP_001247424.1:n.-82-6105G>T
NM_001260496.2:c.404+4219G>T	NP_001247425.1:n.404+4219G>T