Canonical Allele Identifier: CA410686582

Gene: TXNRD2

Linked Data

• dbSNP Id: rs1569081063
• MyVariant Identifiers: chr22:g.19882999C>T (hg19) ; chr22:g.19895476C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895476C>T , CM000684.2:g.19895476C>T	GRCh38
NC_000022.10:g.19882999C>T , CM000684.1:g.19882999C>T	GRCh37
NC_000022.9:g.18262999C>T	NCBI36
NG_011835.1:g.51361G>A , LRG_417:g.51361G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.880G>A MANE Select	ENSP00000383365.1:p.Val294Ile
ENST00000334363.14:c.880G>A	ENSP00000334451.9:p.Val294Ile
ENST00000400518.5:c.790G>A	ENSP00000383362.1:p.Val264Ile
ENST00000400519.6:c.877G>A	ENSP00000383363.1:p.Val293Ile
ENST00000400521.6:c.880G>A	ENSP00000383365.1:p.Val294Ile
ENST00000400525.6:c.811G>A	ENSP00000383369.3:p.Val271Ile
ENST00000474308.5:c.823G>A	ENSP00000485665.1:p.Val275Ile
ENST00000475995.3:c.377G>A
ENST00000491939.6:c.784G>A	ENSP00000485543.1:p.Val262Ile
ENST00000494454.5:n.954G>A
ENST00000542719.6:c.592G>A	ENSP00000485128.2:p.Val198Ile
ENST00000634537.1:c.109G>A	ENSP00000489208.1:p.Val37Ile
ENST00000635155.1:n.466G>A
NM_001282512.1:c.880G>A	NP_001269441.1:p.Val294Ile
NM_006440.4:c.880G>A	NP_006431.2:p.Val294Ile
NM_001282512.2:c.880G>A	NP_001269441.1:p.Val294Ile
NM_001352300.1:c.877G>A	NP_001339229.1:p.Val293Ile
NM_001352301.1:c.790G>A	NP_001339230.1:p.Val264Ile
NM_001352302.1:c.592G>A	NP_001339231.1:p.Val198Ile
NM_001352303.1:c.784G>A	NP_001339232.1:p.Val262Ile
NR_147957.1:n.1012G>A
NM_006440.5:c.880G>A MANE Select	NP_006431.2:p.Val294Ile
NM_001282512.3:c.880G>A	NP_001269441.1:p.Val294Ile
NM_001352300.2:c.877G>A	NP_001339229.1:p.Val293Ile
NR_147957.2:n.838G>A
NM_001352301.2:c.790G>A	NP_001339230.1:p.Val264Ile
NM_001352302.2:c.592G>A	NP_001339231.1:p.Val198Ile
NM_001352303.2:c.784G>A	NP_001339232.1:p.Val262Ile