Canonical Allele Identifier: CA476927484

Gene: RDX

Linked Data

• MyVariant Identifiers: chr11:g.110128908C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.110258183C>T , CM000673.2:g.110258183C>T	GRCh38
NC_000011.9:g.110128908C>T , CM000673.1:g.110128908C>T	GRCh37
NC_000011.8:g.109634118C>T	NCBI36
NG_023044.1:g.43530G>A
NG_023044.2:g.43530G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642511.1:c.432G>A
ENST00000645495.2:c.474G>A MANE Select	ENSP00000496503.2:p.Leu158=
ENST00000645527.1:c.474G>A	ENSP00000496121.1:p.Leu158=
ENST00000646663.1:c.474G>A	ENSP00000494693.1:p.Leu158=
ENST00000647231.1:c.474G>A	ENSP00000496414.1:p.Leu158=
ENST00000343115.8:c.474G>A	ENSP00000342830.4:p.Leu158=
ENST00000405097.5:c.474G>A	ENSP00000384136.1:p.Leu158=
ENST00000528498.5:c.474G>A	ENSP00000432112.1:p.Leu158=
ENST00000528900.5:c.-82-10350G>A	ENSP00000433580.1:n.-82-10350G>A
ENST00000529774.1:n.26G>A
ENST00000530131.5:c.103G>A	ENSP00000432829.1:p.Gly35Arg
ENST00000530301.5:c.378G>A	ENSP00000436277.1:p.Leu126=
ENST00000530749.5:c.474G>A	ENSP00000437301.1:p.Leu158=
ENST00000532118.5:c.441G>A	ENSP00000437140.1:p.Leu147=
ENST00000534683.1:c.-70G>A	ENSP00000431560.1:n.-70G>A
ENST00000544551.5:c.66G>A	ENSP00000445826.1:p.Leu22=
NM_001260492.1:c.474G>A	NP_001247421.1:p.Leu158=
NM_001260493.1:c.474G>A	NP_001247422.1:p.Leu158=
NM_001260494.1:c.66G>A	NP_001247423.1:p.Leu22=
NM_001260495.1:c.-82-10350G>A	NP_001247424.1:n.-82-10350G>A
NM_001260496.1:c.378G>A	NP_001247425.1:p.Leu126=
NM_002906.3:c.474G>A	NP_002897.1:p.Leu158=
NM_001260492.2:c.474G>A	NP_001247421.1:p.Leu158=
NM_002906.4:c.474G>A MANE Select	NP_002897.1:p.Leu158=
NM_001260493.2:c.474G>A	NP_001247422.1:p.Leu158=
NM_001260494.2:c.66G>A	NP_001247423.1:p.Leu22=
NM_001260495.2:c.-82-10350G>A	NP_001247424.1:n.-82-10350G>A
NM_001260496.2:c.378G>A	NP_001247425.1:p.Leu126=