Canonical Allele Identifier: CA410693770

Gene: TXNRD2

Linked Data

• gnomAD v4: 22-19918905-G-T
• MyVariant Identifiers: chr22:g.19906428G>T (hg19) ; chr22:g.19918905G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918905G>T , CM000684.2:g.19918905G>T	GRCh38
NC_000022.10:g.19906428G>T , CM000684.1:g.19906428G>T	GRCh37
NC_000022.9:g.18286428G>T	NCBI36
NG_011835.1:g.27932C>A , LRG_417:g.27932C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.329C>A MANE Select	ENSP00000383365.1:p.Ala110Asp
ENST00000334363.14:c.329C>A	ENSP00000334451.9:p.Ala110Asp
ENST00000400518.5:c.239C>A	ENSP00000383362.1:p.Ala80Asp
ENST00000400519.6:c.326C>A	ENSP00000383363.1:p.Ala109Asp
ENST00000400521.6:c.329C>A	ENSP00000383365.1:p.Ala110Asp
ENST00000400525.6:c.260C>A	ENSP00000383369.3:p.Ala87Asp
ENST00000474308.5:c.272C>A	ENSP00000485665.1:p.Ala91Asp
ENST00000491939.6:c.233C>A	ENSP00000485543.1:p.Ala78Asp
ENST00000496729.2:n.334C>A
ENST00000542719.6:c.41C>A	ENSP00000485128.2:p.Ala14Asp
NM_001282512.1:c.329C>A	NP_001269441.1:p.Ala110Asp
NM_006440.4:c.329C>A	NP_006431.2:p.Ala110Asp
NM_001282512.2:c.329C>A	NP_001269441.1:p.Ala110Asp
NM_001352300.1:c.326C>A	NP_001339229.1:p.Ala109Asp
NM_001352301.1:c.239C>A	NP_001339230.1:p.Ala80Asp
NM_001352302.1:c.41C>A	NP_001339231.1:p.Ala14Asp
NM_001352303.1:c.233C>A	NP_001339232.1:p.Ala78Asp
NR_147957.1:n.461C>A
NM_006440.5:c.329C>A MANE Select	NP_006431.2:p.Ala110Asp
NM_001282512.3:c.329C>A	NP_001269441.1:p.Ala110Asp
NM_001352300.2:c.326C>A	NP_001339229.1:p.Ala109Asp
NR_147957.2:n.287C>A
NM_001352301.2:c.239C>A	NP_001339230.1:p.Ala80Asp
NM_001352302.2:c.41C>A	NP_001339231.1:p.Ala14Asp
NM_001352303.2:c.233C>A	NP_001339232.1:p.Ala78Asp