Canonical Allele Identifier: CA1999752838

Gene: RDX

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.110296518G= , CM000673.2:g.110296518G=	GRCh38
NC_000011.9:g.110167243G= , CM000673.1:g.110167243G=	GRCh37
NC_000011.8:g.109672453G=	NCBI36
NG_023044.1:g.5195C=
NG_023044.2:g.5195C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000645495.2:c.-116C= MANE Select	ENSP00000496503.2:n.-116C=
ENST00000645527.1:c.-324C=	ENSP00000496121.1:n.-324C=
ENST00000647231.1:c.-116C=	ENSP00000496414.1:n.-116C=
ENST00000343115.8:c.-116C=	ENSP00000342830.4:n.-116C=
ENST00000405097.5:c.-116C=	ENSP00000384136.1:n.-116C=
ENST00000528498.5:c.-116C=	ENSP00000432112.1:n.-116C=
ENST00000528556.5:c.-116C=	ENSP00000434881.1:n.-116C=
ENST00000528900.5:c.-210C=	ENSP00000433580.1:n.-210C=
ENST00000530131.5:c.-116C=	ENSP00000432829.1:n.-116C=
ENST00000530301.5:c.-116C=	ENSP00000436277.1:n.-116C=
ENST00000530749.5:c.-116C=	ENSP00000437301.1:n.-116C=
ENST00000533678.1:c.-116C=	ENSP00000435930.1:n.-116C=
ENST00000533991.1:c.-73C=	ENSP00000432572.1:n.-73C=
ENST00000534683.1:c.-233C=	ENSP00000431560.1:n.-233C=
ENST00000544551.5:c.-153C=	ENSP00000445826.1:n.-153C=
NM_001260492.1:c.-116C=	NP_001247421.1:n.-116C=
NM_001260493.1:c.-116C=	NP_001247422.1:n.-116C=
NM_001260494.1:c.-153C=	NP_001247423.1:n.-153C=
NM_001260495.1:c.-210C=	NP_001247424.1:n.-210C=
NM_001260496.1:c.-116C=	NP_001247425.1:n.-116C=
NM_002906.3:c.-116C=	NP_002897.1:n.-116C=
NM_001260492.2:c.-116C=	NP_001247421.1:n.-116C=
NM_002906.4:c.-116C= MANE Select	NP_002897.1:n.-116C=
NM_001260493.2:c.-116C=	NP_001247422.1:n.-116C=
NM_001260494.2:c.-153C=	NP_001247423.1:n.-153C=
NM_001260495.2:c.-210C=	NP_001247424.1:n.-210C=
NM_001260496.2:c.-116C=	NP_001247425.1:n.-116C=