Canonical Allele Identifier: CA1999741016

Gene: RDX

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.110258180T= , CM000673.2:g.110258180T=	GRCh38
NC_000011.9:g.110128905T= , CM000673.1:g.110128905T=	GRCh37
NC_000011.8:g.109634115T=	NCBI36
NG_023044.1:g.43533A=
NG_023044.2:g.43533A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642511.1:c.435A=
ENST00000645495.2:c.477A= MANE Select	ENSP00000496503.2:p.Glu159=
ENST00000645527.1:c.477A=	ENSP00000496121.1:p.Glu159=
ENST00000646663.1:c.477A=	ENSP00000494693.1:p.Glu159=
ENST00000647231.1:c.477A=	ENSP00000496414.1:p.Glu159=
ENST00000343115.8:c.477A=	ENSP00000342830.4:p.Glu159=
ENST00000405097.5:c.477A=	ENSP00000384136.1:p.Glu159=
ENST00000528498.5:c.477A=	ENSP00000432112.1:p.Glu159=
ENST00000528900.5:c.-82-10347A=	ENSP00000433580.1:n.-82-10347A=
ENST00000529774.1:n.29A=
ENST00000530131.5:c.106A=	ENSP00000432829.1:p.Thr36=
ENST00000530301.5:c.381A=	ENSP00000436277.1:p.Glu127=
ENST00000530749.5:c.477A=	ENSP00000437301.1:p.Glu159=
ENST00000532118.5:c.444A=	ENSP00000437140.1:p.Glu148=
ENST00000534683.1:c.-67A=	ENSP00000431560.1:n.-67A=
ENST00000544551.5:c.69A=	ENSP00000445826.1:p.Glu23=
NM_001260492.1:c.477A=	NP_001247421.1:p.Glu159=
NM_001260493.1:c.477A=	NP_001247422.1:p.Glu159=
NM_001260494.1:c.69A=	NP_001247423.1:p.Glu23=
NM_001260495.1:c.-82-10347A=	NP_001247424.1:n.-82-10347A=
NM_001260496.1:c.381A=	NP_001247425.1:p.Glu127=
NM_002906.3:c.477A=	NP_002897.1:p.Glu159=
NM_001260492.2:c.477A=	NP_001247421.1:p.Glu159=
NM_002906.4:c.477A= MANE Select	NP_002897.1:p.Glu159=
NM_001260493.2:c.477A=	NP_001247422.1:p.Glu159=
NM_001260494.2:c.69A=	NP_001247423.1:p.Glu23=
NM_001260495.2:c.-82-10347A=	NP_001247424.1:n.-82-10347A=
NM_001260496.2:c.381A=	NP_001247425.1:p.Glu127=