Canonical Allele Identifier: CA410686605

Gene: TXNRD2

Linked Data

• gnomAD v4: 22-19895487-C-T
• MyVariant Identifiers: chr22:g.19883010C>T (hg19) ; chr22:g.19895487C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895487C>T , CM000684.2:g.19895487C>T	GRCh38
NC_000022.10:g.19883010C>T , CM000684.1:g.19883010C>T	GRCh37
NC_000022.9:g.18263010C>T	NCBI36
NG_011835.1:g.51350G>A , LRG_417:g.51350G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.869G>A MANE Select	ENSP00000383365.1:p.Gly290Asp
ENST00000334363.14:c.869G>A	ENSP00000334451.9:p.Gly290Asp
ENST00000400518.5:c.779G>A	ENSP00000383362.1:p.Gly260Asp
ENST00000400519.6:c.866G>A	ENSP00000383363.1:p.Gly289Asp
ENST00000400521.6:c.869G>A	ENSP00000383365.1:p.Gly290Asp
ENST00000400525.6:c.800G>A	ENSP00000383369.3:p.Gly267Asp
ENST00000474308.5:c.812G>A	ENSP00000485665.1:p.Gly271Asp
ENST00000475995.3:c.366G>A
ENST00000491939.6:c.773G>A	ENSP00000485543.1:p.Gly258Asp
ENST00000494454.5:n.943G>A
ENST00000542719.6:c.581G>A	ENSP00000485128.2:p.Gly194Asp
ENST00000634537.1:c.98G>A	ENSP00000489208.1:p.Gly33Asp
ENST00000635155.1:n.455G>A
NM_001282512.1:c.869G>A	NP_001269441.1:p.Gly290Asp
NM_006440.4:c.869G>A	NP_006431.2:p.Gly290Asp
NM_001282512.2:c.869G>A	NP_001269441.1:p.Gly290Asp
NM_001352300.1:c.866G>A	NP_001339229.1:p.Gly289Asp
NM_001352301.1:c.779G>A	NP_001339230.1:p.Gly260Asp
NM_001352302.1:c.581G>A	NP_001339231.1:p.Gly194Asp
NM_001352303.1:c.773G>A	NP_001339232.1:p.Gly258Asp
NR_147957.1:n.1001G>A
NM_006440.5:c.869G>A MANE Select	NP_006431.2:p.Gly290Asp
NM_001282512.3:c.869G>A	NP_001269441.1:p.Gly290Asp
NM_001352300.2:c.866G>A	NP_001339229.1:p.Gly289Asp
NR_147957.2:n.827G>A
NM_001352301.2:c.779G>A	NP_001339230.1:p.Gly260Asp
NM_001352302.2:c.581G>A	NP_001339231.1:p.Gly194Asp
NM_001352303.2:c.773G>A	NP_001339232.1:p.Gly258Asp