Canonical Allele Identifier: CA2396114614
Gene: TXNRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19940602C= , CM000684.2:g.19940602C= GRCh38
NC_000022.10:g.19928125C= , CM000684.1:g.19928125C= GRCh37
NC_000022.9:g.18308125C= NCBI36
NG_011526.1:g.3863C=
NG_011835.1:g.6235G= , LRG_417:g.6235G=

Transcript Alleles

HGVS Amino-acid change
ENST00000400521.7:c.103+1099G= MANE Select ENSP00000383365.1:n.103+1099G=
ENST00000334363.14:c.103+1099G= ENSP00000334451.9:n.103+1099G=
ENST00000400519.6:c.103+1099G= ENSP00000383363.1:n.103+1099G=
ENST00000400521.6:c.103+1099G= ENSP00000383365.1:n.103+1099G=
ENST00000400525.6:c.103+1099G= ENSP00000383369.3:n.103+1099G=
ENST00000474308.5:c.103+1099G= ENSP00000485665.1:n.103+1099G=
ENST00000496729.2:n.108+1099G=
NM_001282512.1:c.103+1099G= NP_001269441.1:n.103+1099G=
NM_006440.4:c.103+1099G= NP_006431.2:n.103+1099G=
NM_001282512.2:c.103+1099G= NP_001269441.1:n.103+1099G=
NM_001352300.1:c.103+1099G= NP_001339229.1:n.103+1099G=
NR_147957.1:n.292+1099G=
NM_006440.5:c.103+1099G= MANE Select NP_006431.2:n.103+1099G=
NM_001282512.3:c.103+1099G= NP_001269441.1:n.103+1099G=
NM_001352300.2:c.103+1099G= NP_001339229.1:n.103+1099G=
NR_147957.2:n.118+1099G=