Canonical Allele Identifier: CA2615893785

Gene: RDX

Linked Data

• gnomAD v4: 11-110231794-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.110231794A>G , CM000673.2:g.110231794A>G	GRCh38
NC_000011.9:g.110102519A>G , CM000673.1:g.110102519A>G	GRCh37
NC_000011.8:g.109607729A>G	NCBI36
NG_023044.1:g.69919T>C
NG_023044.2:g.69919T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000645312.1:c.391+79T>C
ENST00000645495.2:c.*75T>C MANE Select	ENSP00000496503.2:n.*75T>C
ENST00000645527.1:c.1587+1443T>C	ENSP00000496121.1:n.1587+1443T>C
ENST00000646663.1:c.1748+79T>C	ENSP00000494693.1:n.1748+79T>C
ENST00000647231.1:c.1748+79T>C	ENSP00000496414.1:n.1748+79T>C
ENST00000343115.8:c.*75T>C	ENSP00000342830.4:n.*75T>C
ENST00000405097.5:c.1748+79T>C	ENSP00000384136.1:n.1748+79T>C
ENST00000527537.5:n.1056T>C
ENST00000528498.5:c.1748+79T>C	ENSP00000432112.1:n.1748+79T>C
ENST00000528900.5:c.707+79T>C	ENSP00000433580.1:n.707+79T>C
ENST00000530131.5:c.*1297T>C	ENSP00000432829.1:n.*1297T>C
ENST00000530301.5:c.536+79T>C	ENSP00000436277.1:n.536+79T>C
ENST00000530749.5:c.1748+79T>C	ENSP00000437301.1:n.1748+79T>C
ENST00000532461.5:n.942T>C
ENST00000533961.1:n.527T>C
ENST00000544551.5:c.*75T>C	ENSP00000445826.1:n.*75T>C
NM_001260492.1:c.1748+79T>C	NP_001247421.1:n.1748+79T>C
NM_001260493.1:c.1748+79T>C	NP_001247422.1:n.1748+79T>C
NM_001260494.1:c.*75T>C	NP_001247423.1:n.*75T>C
NM_001260495.1:c.707+79T>C	NP_001247424.1:n.707+79T>C
NM_001260496.1:c.536+79T>C	NP_001247425.1:n.536+79T>C
NM_002906.3:c.*75T>C	NP_002897.1:n.*75T>C
NM_001260492.2:c.1748+79T>C	NP_001247421.1:n.1748+79T>C
NM_002906.4:c.*75T>C MANE Select	NP_002897.1:n.*75T>C
NM_001260493.2:c.1748+79T>C	NP_001247422.1:n.1748+79T>C
NM_001260494.2:c.*75T>C	NP_001247423.1:n.*75T>C
NM_001260495.2:c.707+79T>C	NP_001247424.1:n.707+79T>C
NM_001260496.2:c.536+79T>C	NP_001247425.1:n.536+79T>C