Canonical Allele Identifier: CA513365475
Gene: TXNRD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.19883069A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19895546A>G , CM000684.2:g.19895546A>G GRCh38
NC_000022.10:g.19883069A>G , CM000684.1:g.19883069A>G GRCh37
NC_000022.9:g.18263069A>G NCBI36
NG_011835.1:g.51291T>C , LRG_417:g.51291T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000400521.7:c.810T>C MANE Select ENSP00000383365.1:p.Ser270=
ENST00000334363.14:c.810T>C ENSP00000334451.9:p.Ser270=
ENST00000400518.5:c.720T>C ENSP00000383362.1:p.Ser240=
ENST00000400519.6:c.807T>C ENSP00000383363.1:p.Ser269=
ENST00000400521.6:c.810T>C ENSP00000383365.1:p.Ser270=
ENST00000400525.6:c.741T>C ENSP00000383369.3:p.Ser247=
ENST00000474308.5:c.753T>C ENSP00000485665.1:p.Ser251=
ENST00000475995.3:c.307T>C
ENST00000491939.6:c.714T>C ENSP00000485543.1:p.Ser238=
ENST00000494454.5:n.884T>C
ENST00000542719.6:c.522T>C ENSP00000485128.2:p.Ser174=
ENST00000634537.1:c.39T>C ENSP00000489208.1:p.Ser13=
ENST00000635155.1:n.396T>C
NM_001282512.1:c.810T>C NP_001269441.1:p.Ser270=
NM_006440.4:c.810T>C NP_006431.2:p.Ser270=
NM_001282512.2:c.810T>C NP_001269441.1:p.Ser270=
NM_001352300.1:c.807T>C NP_001339229.1:p.Ser269=
NM_001352301.1:c.720T>C NP_001339230.1:p.Ser240=
NM_001352302.1:c.522T>C NP_001339231.1:p.Ser174=
NM_001352303.1:c.714T>C NP_001339232.1:p.Ser238=
NR_147957.1:n.942T>C
NM_006440.5:c.810T>C MANE Select NP_006431.2:p.Ser270=
NM_001282512.3:c.810T>C NP_001269441.1:p.Ser270=
NM_001352300.2:c.807T>C NP_001339229.1:p.Ser269=
NR_147957.2:n.768T>C
NM_001352301.2:c.720T>C NP_001339230.1:p.Ser240=
NM_001352302.2:c.522T>C NP_001339231.1:p.Ser174=
NM_001352303.2:c.714T>C NP_001339232.1:p.Ser238=