Canonical Allele Identifier: CA10104270

Gene: TXNRD2

Linked Data

• dbSNP Id: rs756174154
• ExAC: 22:19906488 C / T
• gnomAD v2: 22-19906488-C-T
• gnomAD v4: 22-19918965-C-T
• MyVariant Identifiers: chr22:g.19906488C>T (hg19) ; chr22:g.19918965C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918965C>T , CM000684.2:g.19918965C>T	GRCh38
NC_000022.10:g.19906488C>T , CM000684.1:g.19906488C>T	GRCh37
NC_000022.9:g.18286488C>T	NCBI36
NG_011835.1:g.27872G>A , LRG_417:g.27872G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.269G>A MANE Select	ENSP00000383365.1:p.Gly90Asp
ENST00000334363.14:c.269G>A	ENSP00000334451.9:p.Gly90Asp
ENST00000400518.5:c.179G>A	ENSP00000383362.1:p.Gly60Asp
ENST00000400519.6:c.266G>A	ENSP00000383363.1:p.Gly89Asp
ENST00000400521.6:c.269G>A	ENSP00000383365.1:p.Gly90Asp
ENST00000400525.6:c.200G>A	ENSP00000383369.3:p.Gly67Asp
ENST00000474308.5:c.212G>A	ENSP00000485665.1:p.Gly71Asp
ENST00000491939.6:c.173G>A	ENSP00000485543.1:p.Gly58Asp
ENST00000496729.2:n.274G>A
ENST00000542719.6:c.-20G>A	ENSP00000485128.2:n.-20G>A
NM_001282512.1:c.269G>A	NP_001269441.1:p.Gly90Asp
NM_006440.4:c.269G>A	NP_006431.2:p.Gly90Asp
NM_001282512.2:c.269G>A	NP_001269441.1:p.Gly90Asp
NM_001352300.1:c.266G>A	NP_001339229.1:p.Gly89Asp
NM_001352301.1:c.179G>A	NP_001339230.1:p.Gly60Asp
NM_001352302.1:c.-20G>A	NP_001339231.1:n.-20G>A
NM_001352303.1:c.173G>A	NP_001339232.1:p.Gly58Asp
NR_147957.1:n.401G>A
NM_006440.5:c.269G>A MANE Select	NP_006431.2:p.Gly90Asp
NM_001282512.3:c.269G>A	NP_001269441.1:p.Gly90Asp
NM_001352300.2:c.266G>A	NP_001339229.1:p.Gly89Asp
NR_147957.2:n.227G>A
NM_001352301.2:c.179G>A	NP_001339230.1:p.Gly60Asp
NM_001352302.2:c.-20G>A	NP_001339231.1:n.-20G>A
NM_001352303.2:c.173G>A	NP_001339232.1:p.Gly58Asp