Canonical Allele Identifier: CA410686574

Gene: TXNRD2

Linked Data

• dbSNP Id: rs1225557881
• gnomAD v2: 22-19882996-T-A
• gnomAD v4: 22-19895473-T-A
• MyVariant Identifiers: chr22:g.19882996T>A (hg19) ; chr22:g.19895473T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895473T>A , CM000684.2:g.19895473T>A	GRCh38
NC_000022.10:g.19882996T>A , CM000684.1:g.19882996T>A	GRCh37
NC_000022.9:g.18262996T>A	NCBI36
NG_011835.1:g.51364A>T , LRG_417:g.51364A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.883A>T MANE Select	ENSP00000383365.1:p.Thr295Ser
ENST00000334363.14:c.883A>T	ENSP00000334451.9:p.Thr295Ser
ENST00000400518.5:c.793A>T	ENSP00000383362.1:p.Thr265Ser
ENST00000400519.6:c.880A>T	ENSP00000383363.1:p.Thr294Ser
ENST00000400521.6:c.883A>T	ENSP00000383365.1:p.Thr295Ser
ENST00000400525.6:c.814A>T	ENSP00000383369.3:p.Thr272Ser
ENST00000474308.5:c.826A>T	ENSP00000485665.1:p.Thr276Ser
ENST00000475995.3:c.380A>T
ENST00000491939.6:c.787A>T	ENSP00000485543.1:p.Thr263Ser
ENST00000494454.5:n.957A>T
ENST00000542719.6:c.595A>T	ENSP00000485128.2:p.Thr199Ser
ENST00000634537.1:c.112A>T	ENSP00000489208.1:p.Thr38Ser
ENST00000635155.1:n.469A>T
NM_001282512.1:c.883A>T	NP_001269441.1:p.Thr295Ser
NM_006440.4:c.883A>T	NP_006431.2:p.Thr295Ser
NM_001282512.2:c.883A>T	NP_001269441.1:p.Thr295Ser
NM_001352300.1:c.880A>T	NP_001339229.1:p.Thr294Ser
NM_001352301.1:c.793A>T	NP_001339230.1:p.Thr265Ser
NM_001352302.1:c.595A>T	NP_001339231.1:p.Thr199Ser
NM_001352303.1:c.787A>T	NP_001339232.1:p.Thr263Ser
NR_147957.1:n.1015A>T
NM_006440.5:c.883A>T MANE Select	NP_006431.2:p.Thr295Ser
NM_001282512.3:c.883A>T	NP_001269441.1:p.Thr295Ser
NM_001352300.2:c.880A>T	NP_001339229.1:p.Thr294Ser
NR_147957.2:n.841A>T
NM_001352301.2:c.793A>T	NP_001339230.1:p.Thr265Ser
NM_001352302.2:c.595A>T	NP_001339231.1:p.Thr199Ser
NM_001352303.2:c.787A>T	NP_001339232.1:p.Thr263Ser