Canonical Allele Identifier: CA410686649

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19883035A>G (hg19) ; chr22:g.19895512A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895512A>G , CM000684.2:g.19895512A>G	GRCh38
NC_000022.10:g.19883035A>G , CM000684.1:g.19883035A>G	GRCh37
NC_000022.9:g.18263035A>G	NCBI36
NG_011835.1:g.51325T>C , LRG_417:g.51325T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.844T>C MANE Select	ENSP00000383365.1:p.Ser282Pro
ENST00000334363.14:c.844T>C	ENSP00000334451.9:p.Ser282Pro
ENST00000400518.5:c.754T>C	ENSP00000383362.1:p.Ser252Pro
ENST00000400519.6:c.841T>C	ENSP00000383363.1:p.Ser281Pro
ENST00000400521.6:c.844T>C	ENSP00000383365.1:p.Ser282Pro
ENST00000400525.6:c.775T>C	ENSP00000383369.3:p.Ser259Pro
ENST00000474308.5:c.787T>C	ENSP00000485665.1:p.Ser263Pro
ENST00000475995.3:c.341T>C
ENST00000491939.6:c.748T>C	ENSP00000485543.1:p.Ser250Pro
ENST00000494454.5:n.918T>C
ENST00000542719.6:c.556T>C	ENSP00000485128.2:p.Ser186Pro
ENST00000634537.1:c.73T>C	ENSP00000489208.1:p.Ser25Pro
ENST00000635155.1:n.430T>C
NM_001282512.1:c.844T>C	NP_001269441.1:p.Ser282Pro
NM_006440.4:c.844T>C	NP_006431.2:p.Ser282Pro
NM_001282512.2:c.844T>C	NP_001269441.1:p.Ser282Pro
NM_001352300.1:c.841T>C	NP_001339229.1:p.Ser281Pro
NM_001352301.1:c.754T>C	NP_001339230.1:p.Ser252Pro
NM_001352302.1:c.556T>C	NP_001339231.1:p.Ser186Pro
NM_001352303.1:c.748T>C	NP_001339232.1:p.Ser250Pro
NR_147957.1:n.976T>C
NM_006440.5:c.844T>C MANE Select	NP_006431.2:p.Ser282Pro
NM_001282512.3:c.844T>C	NP_001269441.1:p.Ser282Pro
NM_001352300.2:c.841T>C	NP_001339229.1:p.Ser281Pro
NR_147957.2:n.802T>C
NM_001352301.2:c.754T>C	NP_001339230.1:p.Ser252Pro
NM_001352302.2:c.556T>C	NP_001339231.1:p.Ser186Pro
NM_001352303.2:c.748T>C	NP_001339232.1:p.Ser250Pro