Canonical Allele Identifier: CA2396091998
Gene: TXNRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19895522G= , CM000684.2:g.19895522G= GRCh38
NC_000022.10:g.19883045G= , CM000684.1:g.19883045G= GRCh37
NC_000022.9:g.18263045G= NCBI36
NG_011835.1:g.51315C= , LRG_417:g.51315C=

Transcript Alleles

HGVS Amino-acid change
ENST00000400521.7:c.834C= MANE Select ENSP00000383365.1:p.Gly278=
ENST00000334363.14:c.834C= ENSP00000334451.9:p.Gly278=
ENST00000400518.5:c.744C= ENSP00000383362.1:p.Gly248=
ENST00000400519.6:c.831C= ENSP00000383363.1:p.Gly277=
ENST00000400521.6:c.834C= ENSP00000383365.1:p.Gly278=
ENST00000400525.6:c.765C= ENSP00000383369.3:p.Gly255=
ENST00000474308.5:c.777C= ENSP00000485665.1:p.Gly259=
ENST00000475995.3:c.331C=
ENST00000491939.6:c.738C= ENSP00000485543.1:p.Gly246=
ENST00000494454.5:n.908C=
ENST00000542719.6:c.546C= ENSP00000485128.2:p.Gly182=
ENST00000634537.1:c.63C= ENSP00000489208.1:p.Gly21=
ENST00000635155.1:n.420C=
NM_001282512.1:c.834C= NP_001269441.1:p.Gly278=
NM_006440.4:c.834C= NP_006431.2:p.Gly278=
NM_001282512.2:c.834C= NP_001269441.1:p.Gly278=
NM_001352300.1:c.831C= NP_001339229.1:p.Gly277=
NM_001352301.1:c.744C= NP_001339230.1:p.Gly248=
NM_001352302.1:c.546C= NP_001339231.1:p.Gly182=
NM_001352303.1:c.738C= NP_001339232.1:p.Gly246=
NR_147957.1:n.966C=
NM_006440.5:c.834C= MANE Select NP_006431.2:p.Gly278=
NM_001282512.3:c.834C= NP_001269441.1:p.Gly278=
NM_001352300.2:c.831C= NP_001339229.1:p.Gly277=
NR_147957.2:n.792C=
NM_001352301.2:c.744C= NP_001339230.1:p.Gly248=
NM_001352302.2:c.546C= NP_001339231.1:p.Gly182=
NM_001352303.2:c.738C= NP_001339232.1:p.Gly246=