Canonical Allele Identifier: CA2574973628

Gene: RDX

Linked Data

• gnomAD v4: 11-110279708-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.110279710del , CM000673.2:g.110279710del	GRCh38
NC_000011.9:g.110150435del , CM000673.1:g.110150435del	GRCh37
NC_000011.8:g.109655645del	NCBI36
NG_023044.1:g.22004del
NG_023044.2:g.22004del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645495.2:c.-17del MANE Select	ENSP00000496503.2:n.-17del
ENST00000645527.1:c.-17del	ENSP00000496121.1:n.-17del
ENST00000646663.1:c.-17del	ENSP00000494693.1:n.-17del
ENST00000647231.1:c.-17del	ENSP00000496414.1:n.-17del
ENST00000343115.8:c.-17del	ENSP00000342830.4:n.-17del
ENST00000405097.5:c.-17del	ENSP00000384136.1:n.-17del
ENST00000528498.5:c.-17del	ENSP00000432112.1:n.-17del
ENST00000528556.5:c.-17del	ENSP00000434881.1:n.-17del
ENST00000528900.5:c.-111del	ENSP00000433580.1:n.-111del
ENST00000530131.5:c.-17del	ENSP00000432829.1:n.-17del
ENST00000530301.5:c.-17del	ENSP00000436277.1:n.-17del
ENST00000530749.5:c.-17del	ENSP00000437301.1:n.-17del
ENST00000532118.5:c.-21-7090del	ENSP00000437140.1:n.-21-7090del
ENST00000533678.1:c.-17del	ENSP00000435930.1:n.-17del
ENST00000533991.1:c.-21-7090del	ENSP00000432572.1:n.-21-7090del
ENST00000534683.1:c.-138+4del	ENSP00000431560.1:n.-138+4del
ENST00000544551.5:c.-54del	ENSP00000445826.1:n.-54del
NM_001260492.1:c.-17del	NP_001247421.1:n.-17del
NM_001260493.1:c.-17del	NP_001247422.1:n.-17del
NM_001260494.1:c.-54del	NP_001247423.1:n.-54del
NM_001260495.1:c.-111del	NP_001247424.1:n.-111del
NM_001260496.1:c.-17del	NP_001247425.1:n.-17del
NM_002906.3:c.-17del	NP_002897.1:n.-17del
NM_001260492.2:c.-17del	NP_001247421.1:n.-17del
NM_002906.4:c.-17del MANE Select	NP_002897.1:n.-17del
NM_001260493.2:c.-17del	NP_001247422.1:n.-17del
NM_001260494.2:c.-54del	NP_001247423.1:n.-54del
NM_001260495.2:c.-111del	NP_001247424.1:n.-111del
NM_001260496.2:c.-17del	NP_001247425.1:n.-17del