Canonical Allele Identifier: CA410686670

Gene: TXNRD2

Linked Data

• gnomAD v4: 22-19895523-C-T
• MyVariant Identifiers: chr22:g.19883046C>T (hg19) ; chr22:g.19895523C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895523C>T , CM000684.2:g.19895523C>T	GRCh38
NC_000022.10:g.19883046C>T , CM000684.1:g.19883046C>T	GRCh37
NC_000022.9:g.18263046C>T	NCBI36
NG_011835.1:g.51314G>A , LRG_417:g.51314G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.833G>A MANE Select	ENSP00000383365.1:p.Gly278Asp
ENST00000334363.14:c.833G>A	ENSP00000334451.9:p.Gly278Asp
ENST00000400518.5:c.743G>A	ENSP00000383362.1:p.Gly248Asp
ENST00000400519.6:c.830G>A	ENSP00000383363.1:p.Gly277Asp
ENST00000400521.6:c.833G>A	ENSP00000383365.1:p.Gly278Asp
ENST00000400525.6:c.764G>A	ENSP00000383369.3:p.Gly255Asp
ENST00000474308.5:c.776G>A	ENSP00000485665.1:p.Gly259Asp
ENST00000475995.3:c.330G>A
ENST00000491939.6:c.737G>A	ENSP00000485543.1:p.Gly246Asp
ENST00000494454.5:n.907G>A
ENST00000542719.6:c.545G>A	ENSP00000485128.2:p.Gly182Asp
ENST00000634537.1:c.62G>A	ENSP00000489208.1:p.Gly21Asp
ENST00000635155.1:n.419G>A
NM_001282512.1:c.833G>A	NP_001269441.1:p.Gly278Asp
NM_006440.4:c.833G>A	NP_006431.2:p.Gly278Asp
NM_001282512.2:c.833G>A	NP_001269441.1:p.Gly278Asp
NM_001352300.1:c.830G>A	NP_001339229.1:p.Gly277Asp
NM_001352301.1:c.743G>A	NP_001339230.1:p.Gly248Asp
NM_001352302.1:c.545G>A	NP_001339231.1:p.Gly182Asp
NM_001352303.1:c.737G>A	NP_001339232.1:p.Gly246Asp
NR_147957.1:n.965G>A
NM_006440.5:c.833G>A MANE Select	NP_006431.2:p.Gly278Asp
NM_001282512.3:c.833G>A	NP_001269441.1:p.Gly278Asp
NM_001352300.2:c.830G>A	NP_001339229.1:p.Gly277Asp
NR_147957.2:n.791G>A
NM_001352301.2:c.743G>A	NP_001339230.1:p.Gly248Asp
NM_001352302.2:c.545G>A	NP_001339231.1:p.Gly182Asp
NM_001352303.2:c.737G>A	NP_001339232.1:p.Gly246Asp