Canonical Allele Identifier: CA410686571

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19882995G>A (hg19) ; chr22:g.19895472G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895472G>A , CM000684.2:g.19895472G>A	GRCh38
NC_000022.10:g.19882995G>A , CM000684.1:g.19882995G>A	GRCh37
NC_000022.9:g.18262995G>A	NCBI36
NG_011835.1:g.51365C>T , LRG_417:g.51365C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.884C>T MANE Select	ENSP00000383365.1:p.Thr295Ile
ENST00000334363.14:c.884C>T	ENSP00000334451.9:p.Thr295Ile
ENST00000400518.5:c.794C>T	ENSP00000383362.1:p.Thr265Ile
ENST00000400519.6:c.881C>T	ENSP00000383363.1:p.Thr294Ile
ENST00000400521.6:c.884C>T	ENSP00000383365.1:p.Thr295Ile
ENST00000400525.6:c.815C>T	ENSP00000383369.3:p.Thr272Ile
ENST00000474308.5:c.827C>T	ENSP00000485665.1:p.Thr276Ile
ENST00000475995.3:c.381C>T
ENST00000491939.6:c.788C>T	ENSP00000485543.1:p.Thr263Ile
ENST00000494454.5:n.958C>T
ENST00000542719.6:c.596C>T	ENSP00000485128.2:p.Thr199Ile
ENST00000634537.1:c.113C>T	ENSP00000489208.1:p.Thr38Ile
ENST00000635155.1:n.470C>T
NM_001282512.1:c.884C>T	NP_001269441.1:p.Thr295Ile
NM_006440.4:c.884C>T	NP_006431.2:p.Thr295Ile
NM_001282512.2:c.884C>T	NP_001269441.1:p.Thr295Ile
NM_001352300.1:c.881C>T	NP_001339229.1:p.Thr294Ile
NM_001352301.1:c.794C>T	NP_001339230.1:p.Thr265Ile
NM_001352302.1:c.596C>T	NP_001339231.1:p.Thr199Ile
NM_001352303.1:c.788C>T	NP_001339232.1:p.Thr263Ile
NR_147957.1:n.1016C>T
NM_006440.5:c.884C>T MANE Select	NP_006431.2:p.Thr295Ile
NM_001282512.3:c.884C>T	NP_001269441.1:p.Thr295Ile
NM_001352300.2:c.881C>T	NP_001339229.1:p.Thr294Ile
NR_147957.2:n.842C>T
NM_001352301.2:c.794C>T	NP_001339230.1:p.Thr265Ile
NM_001352302.2:c.596C>T	NP_001339231.1:p.Thr199Ile
NM_001352303.2:c.788C>T	NP_001339232.1:p.Thr263Ile