Canonical Allele Identifier: CA410686722

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19883073G>T (hg19) ; chr22:g.19895550G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895550G>T , CM000684.2:g.19895550G>T	GRCh38
NC_000022.10:g.19883073G>T , CM000684.1:g.19883073G>T	GRCh37
NC_000022.9:g.18263073G>T	NCBI36
NG_011835.1:g.51287C>A , LRG_417:g.51287C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.806C>A MANE Select	ENSP00000383365.1:p.Ala269Glu
ENST00000334363.14:c.806C>A	ENSP00000334451.9:p.Ala269Glu
ENST00000400518.5:c.716C>A	ENSP00000383362.1:p.Ala239Glu
ENST00000400519.6:c.803C>A	ENSP00000383363.1:p.Ala268Glu
ENST00000400521.6:c.806C>A	ENSP00000383365.1:p.Ala269Glu
ENST00000400525.6:c.737C>A	ENSP00000383369.3:p.Ala246Glu
ENST00000474308.5:c.749C>A	ENSP00000485665.1:p.Ala250Glu
ENST00000475995.3:c.303C>A
ENST00000491939.6:c.710C>A	ENSP00000485543.1:p.Ala237Glu
ENST00000494454.5:n.880C>A
ENST00000542719.6:c.518C>A	ENSP00000485128.2:p.Ala173Glu
ENST00000634537.1:c.35C>A	ENSP00000489208.1:p.Ala12Glu
ENST00000635155.1:n.392C>A
NM_001282512.1:c.806C>A	NP_001269441.1:p.Ala269Glu
NM_006440.4:c.806C>A	NP_006431.2:p.Ala269Glu
NM_001282512.2:c.806C>A	NP_001269441.1:p.Ala269Glu
NM_001352300.1:c.803C>A	NP_001339229.1:p.Ala268Glu
NM_001352301.1:c.716C>A	NP_001339230.1:p.Ala239Glu
NM_001352302.1:c.518C>A	NP_001339231.1:p.Ala173Glu
NM_001352303.1:c.710C>A	NP_001339232.1:p.Ala237Glu
NR_147957.1:n.938C>A
NM_006440.5:c.806C>A MANE Select	NP_006431.2:p.Ala269Glu
NM_001282512.3:c.806C>A	NP_001269441.1:p.Ala269Glu
NM_001352300.2:c.803C>A	NP_001339229.1:p.Ala268Glu
NR_147957.2:n.764C>A
NM_001352301.2:c.716C>A	NP_001339230.1:p.Ala239Glu
NM_001352302.2:c.518C>A	NP_001339231.1:p.Ala173Glu
NM_001352303.2:c.710C>A	NP_001339232.1:p.Ala237Glu