Canonical Allele Identifier: CA513365159

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19882961C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895438C>A , CM000684.2:g.19895438C>A	GRCh38
NC_000022.10:g.19882961C>A , CM000684.1:g.19882961C>A	GRCh37
NC_000022.9:g.18262961C>A	NCBI36
NG_011835.1:g.51399G>T , LRG_417:g.51399G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.918G>T MANE Select	ENSP00000383365.1:p.Thr306=
ENST00000334363.14:c.918G>T	ENSP00000334451.9:p.Thr306=
ENST00000400518.5:c.828G>T	ENSP00000383362.1:p.Thr276=
ENST00000400519.6:c.915G>T	ENSP00000383363.1:p.Thr305=
ENST00000400521.6:c.918G>T	ENSP00000383365.1:p.Thr306=
ENST00000400525.6:c.849G>T	ENSP00000383369.3:p.Thr283=
ENST00000474308.5:c.861G>T	ENSP00000485665.1:p.Thr287=
ENST00000475995.3:c.415G>T
ENST00000491939.6:c.822G>T	ENSP00000485543.1:p.Thr274=
ENST00000494454.5:n.992G>T
ENST00000542719.6:c.630G>T	ENSP00000485128.2:p.Thr210=
ENST00000634537.1:c.147G>T	ENSP00000489208.1:p.Thr49=
ENST00000635155.1:n.504G>T
NM_001282512.1:c.918G>T	NP_001269441.1:p.Thr306=
NM_006440.4:c.918G>T	NP_006431.2:p.Thr306=
NM_001282512.2:c.918G>T	NP_001269441.1:p.Thr306=
NM_001352300.1:c.915G>T	NP_001339229.1:p.Thr305=
NM_001352301.1:c.828G>T	NP_001339230.1:p.Thr276=
NM_001352302.1:c.630G>T	NP_001339231.1:p.Thr210=
NM_001352303.1:c.822G>T	NP_001339232.1:p.Thr274=
NR_147957.1:n.1050G>T
NM_006440.5:c.918G>T MANE Select	NP_006431.2:p.Thr306=
NM_001282512.3:c.918G>T	NP_001269441.1:p.Thr306=
NM_001352300.2:c.915G>T	NP_001339229.1:p.Thr305=
NR_147957.2:n.876G>T
NM_001352301.2:c.828G>T	NP_001339230.1:p.Thr276=
NM_001352302.2:c.630G>T	NP_001339231.1:p.Thr210=
NM_001352303.2:c.822G>T	NP_001339232.1:p.Thr274=