Canonical Allele Identifier: CA1999720898

Gene: RDX

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.110231889C= , CM000673.2:g.110231889C=	GRCh38
NC_000011.9:g.110102614C= , CM000673.1:g.110102614C=	GRCh37
NC_000011.8:g.109607824C=	NCBI36
NG_023044.1:g.69824G=
NG_023044.2:g.69824G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645312.1:c.375G=
ENST00000645495.2:c.1732G= MANE Select	ENSP00000496503.2:p.Asp578=
ENST00000645527.1:c.1587+1348G=	ENSP00000496121.1:n.1587+1348G=
ENST00000646663.1:c.1732G=	ENSP00000494693.1:p.Asp578=
ENST00000647231.1:c.1732G=	ENSP00000496414.1:p.Asp578=
ENST00000343115.8:c.1732G=	ENSP00000342830.4:p.Asp578=
ENST00000405097.5:c.1732G=	ENSP00000384136.1:p.Asp578=
ENST00000527537.5:n.961G=
ENST00000528498.5:c.1732G=	ENSP00000432112.1:p.Asp578=
ENST00000528900.5:c.691G=	ENSP00000433580.1:p.Asp231=
ENST00000530085.2:n.742G=
ENST00000530131.5:c.*1202G=	ENSP00000432829.1:n.*1202G=
ENST00000530301.5:c.520G=	ENSP00000436277.1:p.Asp174=
ENST00000530749.5:c.1732G=	ENSP00000437301.1:p.Asp578=
ENST00000532461.5:n.847G=
ENST00000533961.1:n.432G=
ENST00000544551.5:c.1324G=	ENSP00000445826.1:p.Asp442=
NM_001260492.1:c.1732G=	NP_001247421.1:p.Asp578=
NM_001260493.1:c.1732G=	NP_001247422.1:p.Asp578=
NM_001260494.1:c.1324G=	NP_001247423.1:p.Asp442=
NM_001260495.1:c.691G=	NP_001247424.1:p.Asp231=
NM_001260496.1:c.520G=	NP_001247425.1:p.Asp174=
NM_002906.3:c.1732G=	NP_002897.1:p.Asp578=
NM_001260492.2:c.1732G=	NP_001247421.1:p.Asp578=
NM_002906.4:c.1732G= MANE Select	NP_002897.1:p.Asp578=
NM_001260493.2:c.1732G=	NP_001247422.1:p.Asp578=
NM_001260494.2:c.1324G=	NP_001247423.1:p.Asp442=
NM_001260495.2:c.691G=	NP_001247424.1:p.Asp231=
NM_001260496.2:c.520G=	NP_001247425.1:p.Asp174=