Canonical Allele Identifier: CA410693785
Gene: TXNRD2 HGNC NCBI

Linked Data

dbSNP Id: rs1365322316

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19918909C>T , CM000684.2:g.19918909C>T GRCh38
NC_000022.10:g.19906432C>T , CM000684.1:g.19906432C>T GRCh37
NC_000022.9:g.18286432C>T NCBI36
NG_011835.1:g.27928G>A , LRG_417:g.27928G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000400521.7:c.325G>A MANE Select ENSP00000383365.1:p.Asp109Asn
ENST00000334363.14:c.325G>A ENSP00000334451.9:p.Asp109Asn
ENST00000400518.5:c.235G>A ENSP00000383362.1:p.Asp79Asn
ENST00000400519.6:c.322G>A ENSP00000383363.1:p.Asp108Asn
ENST00000400521.6:c.325G>A ENSP00000383365.1:p.Asp109Asn
ENST00000400525.6:c.256G>A ENSP00000383369.3:p.Asp86Asn
ENST00000474308.5:c.268G>A ENSP00000485665.1:p.Asp90Asn
ENST00000491939.6:c.229G>A ENSP00000485543.1:p.Asp77Asn
ENST00000496729.2:n.330G>A
ENST00000542719.6:c.37G>A ENSP00000485128.2:p.Asp13Asn
NM_001282512.1:c.325G>A NP_001269441.1:p.Asp109Asn
NM_006440.4:c.325G>A NP_006431.2:p.Asp109Asn
NM_001282512.2:c.325G>A NP_001269441.1:p.Asp109Asn
NM_001352300.1:c.322G>A NP_001339229.1:p.Asp108Asn
NM_001352301.1:c.235G>A NP_001339230.1:p.Asp79Asn
NM_001352302.1:c.37G>A NP_001339231.1:p.Asp13Asn
NM_001352303.1:c.229G>A NP_001339232.1:p.Asp77Asn
NR_147957.1:n.457G>A
NM_006440.5:c.325G>A MANE Select NP_006431.2:p.Asp109Asn
NM_001282512.3:c.325G>A NP_001269441.1:p.Asp109Asn
NM_001352300.2:c.322G>A NP_001339229.1:p.Asp108Asn
NR_147957.2:n.283G>A
NM_001352301.2:c.235G>A NP_001339230.1:p.Asp79Asn
NM_001352302.2:c.37G>A NP_001339231.1:p.Asp13Asn
NM_001352303.2:c.229G>A NP_001339232.1:p.Asp77Asn