Canonical Allele Identifier: CA1999720862

Gene: RDX

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.110231798T= , CM000673.2:g.110231798T=	GRCh38
NC_000011.9:g.110102523T= , CM000673.1:g.110102523T=	GRCh37
NC_000011.8:g.109607733T=	NCBI36
NG_023044.1:g.69915A=
NG_023044.2:g.69915A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000645312.1:c.391+75A=
ENST00000645495.2:c.*71A= MANE Select	ENSP00000496503.2:n.*71A=
ENST00000645527.1:c.1587+1439A=	ENSP00000496121.1:n.1587+1439A=
ENST00000646663.1:c.1748+75A=	ENSP00000494693.1:n.1748+75A=
ENST00000647231.1:c.1748+75A=	ENSP00000496414.1:n.1748+75A=
ENST00000343115.8:c.*71A=	ENSP00000342830.4:n.*71A=
ENST00000405097.5:c.1748+75A=	ENSP00000384136.1:n.1748+75A=
ENST00000527537.5:n.1052A=
ENST00000528498.5:c.1748+75A=	ENSP00000432112.1:n.1748+75A=
ENST00000528900.5:c.707+75A=	ENSP00000433580.1:n.707+75A=
ENST00000530131.5:c.*1293A=	ENSP00000432829.1:n.*1293A=
ENST00000530301.5:c.536+75A=	ENSP00000436277.1:n.536+75A=
ENST00000530749.5:c.1748+75A=	ENSP00000437301.1:n.1748+75A=
ENST00000532461.5:n.938A=
ENST00000533961.1:n.523A=
ENST00000544551.5:c.*71A=	ENSP00000445826.1:n.*71A=
NM_001260492.1:c.1748+75A=	NP_001247421.1:n.1748+75A=
NM_001260493.1:c.1748+75A=	NP_001247422.1:n.1748+75A=
NM_001260494.1:c.*71A=	NP_001247423.1:n.*71A=
NM_001260495.1:c.707+75A=	NP_001247424.1:n.707+75A=
NM_001260496.1:c.536+75A=	NP_001247425.1:n.536+75A=
NM_002906.3:c.*71A=	NP_002897.1:n.*71A=
NM_001260492.2:c.1748+75A=	NP_001247421.1:n.1748+75A=
NM_002906.4:c.*71A= MANE Select	NP_002897.1:n.*71A=
NM_001260493.2:c.1748+75A=	NP_001247422.1:n.1748+75A=
NM_001260494.2:c.*71A=	NP_001247423.1:n.*71A=
NM_001260495.2:c.707+75A=	NP_001247424.1:n.707+75A=
NM_001260496.2:c.536+75A=	NP_001247425.1:n.536+75A=