Canonical Allele Identifier: CA2615895289

Gene: RDX

Linked Data

• gnomAD v4: 11-110279740-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.110279740A>G , CM000673.2:g.110279740A>G	GRCh38
NC_000011.9:g.110150465A>G , CM000673.1:g.110150465A>G	GRCh37
NC_000011.8:g.109655675A>G	NCBI36
NG_023044.1:g.21973T>C
NG_023044.2:g.21973T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645495.2:c.-48T>C MANE Select	ENSP00000496503.2:n.-48T>C
ENST00000645527.1:c.-48T>C	ENSP00000496121.1:n.-48T>C
ENST00000646663.1:c.-48T>C	ENSP00000494693.1:n.-48T>C
ENST00000647231.1:c.-48T>C	ENSP00000496414.1:n.-48T>C
ENST00000343115.8:c.-48T>C	ENSP00000342830.4:n.-48T>C
ENST00000405097.5:c.-48T>C	ENSP00000384136.1:n.-48T>C
ENST00000528498.5:c.-48T>C	ENSP00000432112.1:n.-48T>C
ENST00000528556.5:c.-48T>C	ENSP00000434881.1:n.-48T>C
ENST00000528900.5:c.-142T>C	ENSP00000433580.1:n.-142T>C
ENST00000530131.5:c.-48T>C	ENSP00000432829.1:n.-48T>C
ENST00000530301.5:c.-48T>C	ENSP00000436277.1:n.-48T>C
ENST00000530749.5:c.-48T>C	ENSP00000437301.1:n.-48T>C
ENST00000532118.5:c.-21-7121T>C	ENSP00000437140.1:n.-21-7121T>C
ENST00000533678.1:c.-48T>C	ENSP00000435930.1:n.-48T>C
ENST00000533991.1:c.-21-7121T>C	ENSP00000432572.1:n.-21-7121T>C
ENST00000534683.1:c.-165T>C	ENSP00000431560.1:n.-165T>C
ENST00000544551.5:c.-85T>C	ENSP00000445826.1:n.-85T>C
NM_001260492.1:c.-48T>C	NP_001247421.1:n.-48T>C
NM_001260493.1:c.-48T>C	NP_001247422.1:n.-48T>C
NM_001260494.1:c.-85T>C	NP_001247423.1:n.-85T>C
NM_001260495.1:c.-142T>C	NP_001247424.1:n.-142T>C
NM_001260496.1:c.-48T>C	NP_001247425.1:n.-48T>C
NM_002906.3:c.-48T>C	NP_002897.1:n.-48T>C
NM_001260492.2:c.-48T>C	NP_001247421.1:n.-48T>C
NM_002906.4:c.-48T>C MANE Select	NP_002897.1:n.-48T>C
NM_001260493.2:c.-48T>C	NP_001247422.1:n.-48T>C
NM_001260494.2:c.-85T>C	NP_001247423.1:n.-85T>C
NM_001260495.2:c.-142T>C	NP_001247424.1:n.-142T>C
NM_001260496.2:c.-48T>C	NP_001247425.1:n.-48T>C