Canonical Allele Identifier: CA476928386

Gene: RDX

Linked Data

• MyVariant Identifiers: chr11:g.110150406T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.110279681T>A , CM000673.2:g.110279681T>A	GRCh38
NC_000011.9:g.110150406T>A , CM000673.1:g.110150406T>A	GRCh37
NC_000011.8:g.109655616T>A	NCBI36
NG_023044.1:g.22032A>T
NG_023044.2:g.22032A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645495.2:c.12A>T MANE Select	ENSP00000496503.2:p.Pro4=
ENST00000645527.1:c.12A>T	ENSP00000496121.1:p.Pro4=
ENST00000646663.1:c.12A>T	ENSP00000494693.1:p.Pro4=
ENST00000647231.1:c.12A>T	ENSP00000496414.1:p.Pro4=
ENST00000343115.8:c.12A>T	ENSP00000342830.4:p.Pro4=
ENST00000405097.5:c.12A>T	ENSP00000384136.1:p.Pro4=
ENST00000528498.5:c.12A>T	ENSP00000432112.1:p.Pro4=
ENST00000528556.5:c.12A>T	ENSP00000434881.1:p.Pro4=
ENST00000528900.5:c.-83A>T	ENSP00000433580.1:n.-83A>T
ENST00000530131.5:c.12A>T	ENSP00000432829.1:p.Pro4=
ENST00000530301.5:c.12A>T	ENSP00000436277.1:p.Pro4=
ENST00000530749.5:c.12A>T	ENSP00000437301.1:p.Pro4=
ENST00000532118.5:c.-21-7062A>T	ENSP00000437140.1:n.-21-7062A>T
ENST00000533678.1:c.12A>T	ENSP00000435930.1:p.Pro4=
ENST00000533991.1:c.-21-7062A>T	ENSP00000432572.1:n.-21-7062A>T
ENST00000534683.1:c.-138+32A>T	ENSP00000431560.1:n.-138+32A>T
ENST00000544551.5:c.-26A>T	ENSP00000445826.1:n.-26A>T
NM_001260492.1:c.12A>T	NP_001247421.1:p.Pro4=
NM_001260493.1:c.12A>T	NP_001247422.1:p.Pro4=
NM_001260494.1:c.-26A>T	NP_001247423.1:n.-26A>T
NM_001260495.1:c.-83A>T	NP_001247424.1:n.-83A>T
NM_001260496.1:c.12A>T	NP_001247425.1:p.Pro4=
NM_002906.3:c.12A>T	NP_002897.1:p.Pro4=
NM_001260492.2:c.12A>T	NP_001247421.1:p.Pro4=
NM_002906.4:c.12A>T MANE Select	NP_002897.1:p.Pro4=
NM_001260493.2:c.12A>T	NP_001247422.1:p.Pro4=
NM_001260494.2:c.-26A>T	NP_001247423.1:n.-26A>T
NM_001260495.2:c.-83A>T	NP_001247424.1:n.-83A>T
NM_001260496.2:c.12A>T	NP_001247425.1:p.Pro4=