Canonical Allele Identifier: CA410694108

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19906525T>G (hg19) ; chr22:g.19919002T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19919002T>G , CM000684.2:g.19919002T>G	GRCh38
NC_000022.10:g.19906525T>G , CM000684.1:g.19906525T>G	GRCh37
NC_000022.9:g.18286525T>G	NCBI36
NG_011835.1:g.27835A>C , LRG_417:g.27835A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.232A>C MANE Select	ENSP00000383365.1:p.Thr78Pro
ENST00000334363.14:c.232A>C	ENSP00000334451.9:p.Thr78Pro
ENST00000400518.5:c.142A>C	ENSP00000383362.1:p.Thr48Pro
ENST00000400519.6:c.229A>C	ENSP00000383363.1:p.Thr77Pro
ENST00000400521.6:c.232A>C	ENSP00000383365.1:p.Thr78Pro
ENST00000400525.6:c.163A>C	ENSP00000383369.3:p.Thr55Pro
ENST00000474308.5:c.175A>C	ENSP00000485665.1:p.Thr59Pro
ENST00000491939.6:c.136A>C	ENSP00000485543.1:p.Thr46Pro
ENST00000496729.2:n.237A>C
ENST00000542719.6:c.-57A>C	ENSP00000485128.2:n.-57A>C
NM_001282512.1:c.232A>C	NP_001269441.1:p.Thr78Pro
NM_006440.4:c.232A>C	NP_006431.2:p.Thr78Pro
NM_001282512.2:c.232A>C	NP_001269441.1:p.Thr78Pro
NM_001352300.1:c.229A>C	NP_001339229.1:p.Thr77Pro
NM_001352301.1:c.142A>C	NP_001339230.1:p.Thr48Pro
NM_001352302.1:c.-57A>C	NP_001339231.1:n.-57A>C
NM_001352303.1:c.136A>C	NP_001339232.1:p.Thr46Pro
NR_147957.1:n.364A>C
NM_006440.5:c.232A>C MANE Select	NP_006431.2:p.Thr78Pro
NM_001282512.3:c.232A>C	NP_001269441.1:p.Thr78Pro
NM_001352300.2:c.229A>C	NP_001339229.1:p.Thr77Pro
NR_147957.2:n.190A>C
NM_001352301.2:c.142A>C	NP_001339230.1:p.Thr48Pro
NM_001352302.2:c.-57A>C	NP_001339231.1:n.-57A>C
NM_001352303.2:c.136A>C	NP_001339232.1:p.Thr46Pro