Canonical Allele Identifier: CA15683351

Gene: RDX

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.110258269C>G , CM000673.2:g.110258269C>G	GRCh38
NC_000011.9:g.110128994C>G , CM000673.1:g.110128994C>G	GRCh37
NC_000011.8:g.109634204C>G	NCBI36
NG_023044.1:g.43444G>C
NG_023044.2:g.43444G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_002906.4:c.468-80G>C MANE Select	NP_002897.1:n.468-80G>C
ENST00000645495.2:c.468-80G>C MANE Select	ENSP00000496503.2:n.468-80G>C
NM_001260492.1:c.468-80G>C	NP_001247421.1:n.468-80G>C
NM_001260492.2:c.468-80G>C	NP_001247421.1:n.468-80G>C
NM_001260493.1:c.468-80G>C	NP_001247422.1:n.468-80G>C
NM_001260493.2:c.468-80G>C	NP_001247422.1:n.468-80G>C
NM_001260494.1:c.60-80G>C	NP_001247423.1:n.60-80G>C
NM_001260494.2:c.60-80G>C	NP_001247423.1:n.60-80G>C
NM_001260495.1:c.-82-10436G>C	NP_001247424.1:n.-82-10436G>C
NM_001260495.2:c.-82-10436G>C	NP_001247424.1:n.-82-10436G>C
NM_001260496.1:c.372-80G>C	NP_001247425.1:n.372-80G>C
NM_001260496.2:c.372-80G>C	NP_001247425.1:n.372-80G>C
NM_002906.3:c.468-80G>C	NP_002897.1:n.468-80G>C
ENST00000343115.8:c.468-80G>C	ENSP00000342830.4:n.468-80G>C
ENST00000405097.5:c.468-80G>C	ENSP00000384136.1:n.468-80G>C
ENST00000528498.5:c.468-80G>C	ENSP00000432112.1:n.468-80G>C
ENST00000528900.5:c.-82-10436G>C	ENSP00000433580.1:n.-82-10436G>C
ENST00000530131.5:c.97-80G>C	ENSP00000432829.1:n.97-80G>C
ENST00000530301.5:c.372-80G>C	ENSP00000436277.1:n.372-80G>C
ENST00000530749.5:c.468-80G>C	ENSP00000437301.1:n.468-80G>C
ENST00000532118.5:c.435-80G>C	ENSP00000437140.1:n.435-80G>C
ENST00000534683.1:c.-76-80G>C	ENSP00000431560.1:n.-76-80G>C
ENST00000544551.5:c.60-80G>C	ENSP00000445826.1:n.60-80G>C
ENST00000642511.1:c.426-80G>C
ENST00000645527.1:c.468-80G>C	ENSP00000496121.1:n.468-80G>C
ENST00000646663.1:c.468-80G>C	ENSP00000494693.1:n.468-80G>C
ENST00000647231.1:c.468-80G>C	ENSP00000496414.1:n.468-80G>C