Canonical Allele Identifier: CA410686339

Gene: TXNRD2

Linked Data

• dbSNP Id: rs2145969776
• MyVariant Identifiers: chr22:g.19882947G>T (hg19) ; chr22:g.19895424G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895424G>T , CM000684.2:g.19895424G>T	GRCh38
NC_000022.10:g.19882947G>T , CM000684.1:g.19882947G>T	GRCh37
NC_000022.9:g.18262947G>T	NCBI36
NG_011835.1:g.51413C>A , LRG_417:g.51413C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.932C>A MANE Select	ENSP00000383365.1:p.Thr311Asn
ENST00000334363.14:c.932C>A	ENSP00000334451.9:p.Thr311Asn
ENST00000400518.5:c.842C>A	ENSP00000383362.1:p.Thr281Asn
ENST00000400519.6:c.929C>A	ENSP00000383363.1:p.Thr310Asn
ENST00000400521.6:c.932C>A	ENSP00000383365.1:p.Thr311Asn
ENST00000400525.6:c.863C>A	ENSP00000383369.3:p.Thr288Asn
ENST00000474308.5:c.875C>A	ENSP00000485665.1:p.Thr292Asn
ENST00000475995.3:c.429C>A
ENST00000491939.6:c.836C>A	ENSP00000485543.1:p.Thr279Asn
ENST00000494454.5:n.1006C>A
ENST00000542719.6:c.644C>A	ENSP00000485128.2:p.Thr215Asn
ENST00000634537.1:c.161C>A	ENSP00000489208.1:p.Thr54Asn
ENST00000635155.1:n.518C>A
NM_001282512.1:c.932C>A	NP_001269441.1:p.Thr311Asn
NM_006440.4:c.932C>A	NP_006431.2:p.Thr311Asn
NM_001282512.2:c.932C>A	NP_001269441.1:p.Thr311Asn
NM_001352300.1:c.929C>A	NP_001339229.1:p.Thr310Asn
NM_001352301.1:c.842C>A	NP_001339230.1:p.Thr281Asn
NM_001352302.1:c.644C>A	NP_001339231.1:p.Thr215Asn
NM_001352303.1:c.836C>A	NP_001339232.1:p.Thr279Asn
NR_147957.1:n.1064C>A
NM_006440.5:c.932C>A MANE Select	NP_006431.2:p.Thr311Asn
NM_001282512.3:c.932C>A	NP_001269441.1:p.Thr311Asn
NM_001352300.2:c.929C>A	NP_001339229.1:p.Thr310Asn
NR_147957.2:n.890C>A
NM_001352301.2:c.842C>A	NP_001339230.1:p.Thr281Asn
NM_001352302.2:c.644C>A	NP_001339231.1:p.Thr215Asn
NM_001352303.2:c.836C>A	NP_001339232.1:p.Thr279Asn