Canonical Allele Identifier: CA3182810888

Gene: RDX

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.110236135C= , CM000673.2:g.110236135C=	GRCh38
NC_000011.9:g.110106860C= , CM000673.1:g.110106860C=	GRCh37
NC_000011.8:g.109612070C=	NCBI36
NG_023044.1:g.65578G=
NG_023044.2:g.65578G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645495.2:c.1308G= MANE Select	ENSP00000496503.2:p.Lys436=
ENST00000645527.1:c.1308G=	ENSP00000496121.1:p.Lys436=
ENST00000646663.1:c.1308G=	ENSP00000494693.1:p.Lys436=
ENST00000647231.1:c.1308G=	ENSP00000496414.1:p.Lys436=
ENST00000343115.8:c.1308G=	ENSP00000342830.4:p.Lys436=
ENST00000405097.5:c.1308G=	ENSP00000384136.1:p.Lys436=
ENST00000527537.5:n.537G=
ENST00000528498.5:c.1308G=	ENSP00000432112.1:p.Lys436=
ENST00000528900.5:c.267G=	ENSP00000433580.1:p.Lys89=
ENST00000530085.2:n.318G=
ENST00000530131.5:c.*778G=	ENSP00000432829.1:n.*778G=
ENST00000530301.5:c.405-4131G=	ENSP00000436277.1:n.405-4131G=
ENST00000530749.5:c.1308G=	ENSP00000437301.1:p.Lys436=
ENST00000532461.5:n.423G=
ENST00000544551.5:c.900G=	ENSP00000445826.1:p.Lys300=
NM_001260492.1:c.1308G=	NP_001247421.1:p.Lys436=
NM_001260493.1:c.1308G=	NP_001247422.1:p.Lys436=
NM_001260494.1:c.900G=	NP_001247423.1:p.Lys300=
NM_001260495.1:c.267G=	NP_001247424.1:p.Lys89=
NM_001260496.1:c.405-4131G=	NP_001247425.1:n.405-4131G=
NM_002906.3:c.1308G=	NP_002897.1:p.Lys436=
NM_001260492.2:c.1308G=	NP_001247421.1:p.Lys436=
NM_002906.4:c.1308G= MANE Select	NP_002897.1:p.Lys436=
NM_001260493.2:c.1308G=	NP_001247422.1:p.Lys436=
NM_001260494.2:c.900G=	NP_001247423.1:p.Lys300=
NM_001260495.2:c.267G=	NP_001247424.1:p.Lys89=
NM_001260496.2:c.405-4131G=	NP_001247425.1:n.405-4131G=