Canonical Allele Identifier: CA382868191

Gene: RDX

Linked Data

• gnomAD v4: 11-110258122-G-T
• MyVariant Identifiers: chr11:g.110128847G>T (hg19) ; chr11:g.110258122G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.110258122G>T , CM000673.2:g.110258122G>T	GRCh38
NC_000011.9:g.110128847G>T , CM000673.1:g.110128847G>T	GRCh37
NC_000011.8:g.109634057G>T	NCBI36
NG_023044.1:g.43591C>A
NG_023044.2:g.43591C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642511.1:c.493C>A
ENST00000645495.2:c.535C>A MANE Select	ENSP00000496503.2:p.His179Asn
ENST00000645527.1:c.535C>A	ENSP00000496121.1:p.His179Asn
ENST00000646663.1:c.535C>A	ENSP00000494693.1:p.His179Asn
ENST00000647231.1:c.535C>A	ENSP00000496414.1:p.His179Asn
ENST00000343115.8:c.535C>A	ENSP00000342830.4:p.His179Asn
ENST00000405097.5:c.535C>A	ENSP00000384136.1:p.His179Asn
ENST00000528498.5:c.535C>A	ENSP00000432112.1:p.His179Asn
ENST00000528900.5:c.-82-10289C>A	ENSP00000433580.1:n.-82-10289C>A
ENST00000529774.1:n.87C>A
ENST00000530131.5:c.*5C>A	ENSP00000432829.1:n.*5C>A
ENST00000530301.5:c.404+35C>A	ENSP00000436277.1:n.404+35C>A
ENST00000530749.5:c.535C>A	ENSP00000437301.1:p.His179Asn
ENST00000534683.1:c.-9C>A	ENSP00000431560.1:n.-9C>A
ENST00000544551.5:c.127C>A	ENSP00000445826.1:p.His43Asn
NM_001260492.1:c.535C>A	NP_001247421.1:p.His179Asn
NM_001260493.1:c.535C>A	NP_001247422.1:p.His179Asn
NM_001260494.1:c.127C>A	NP_001247423.1:p.His43Asn
NM_001260495.1:c.-82-10289C>A	NP_001247424.1:n.-82-10289C>A
NM_001260496.1:c.404+35C>A	NP_001247425.1:n.404+35C>A
NM_002906.3:c.535C>A	NP_002897.1:p.His179Asn
NM_001260492.2:c.535C>A	NP_001247421.1:p.His179Asn
NM_002906.4:c.535C>A MANE Select	NP_002897.1:p.His179Asn
NM_001260493.2:c.535C>A	NP_001247422.1:p.His179Asn
NM_001260494.2:c.127C>A	NP_001247423.1:p.His43Asn
NM_001260495.2:c.-82-10289C>A	NP_001247424.1:n.-82-10289C>A
NM_001260496.2:c.404+35C>A	NP_001247425.1:n.404+35C>A