Canonical Allele Identifier: CA410694072

Gene: TXNRD2

Linked Data

• dbSNP Id: rs1157557232
• gnomAD v2: 22-19906515-C-T
• gnomAD v4: 22-19918992-C-T
• MyVariant Identifiers: chr22:g.19906515C>T (hg19) ; chr22:g.19918992C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918992C>T , CM000684.2:g.19918992C>T	GRCh38
NC_000022.10:g.19906515C>T , CM000684.1:g.19906515C>T	GRCh37
NC_000022.9:g.18286515C>T	NCBI36
NG_011835.1:g.27845G>A , LRG_417:g.27845G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.242G>A MANE Select	ENSP00000383365.1:p.Gly81Asp
ENST00000334363.14:c.242G>A	ENSP00000334451.9:p.Gly81Asp
ENST00000400518.5:c.152G>A	ENSP00000383362.1:p.Gly51Asp
ENST00000400519.6:c.239G>A	ENSP00000383363.1:p.Gly80Asp
ENST00000400521.6:c.242G>A	ENSP00000383365.1:p.Gly81Asp
ENST00000400525.6:c.173G>A	ENSP00000383369.3:p.Gly58Asp
ENST00000474308.5:c.185G>A	ENSP00000485665.1:p.Gly62Asp
ENST00000491939.6:c.146G>A	ENSP00000485543.1:p.Gly49Asp
ENST00000496729.2:n.247G>A
ENST00000542719.6:c.-47G>A	ENSP00000485128.2:n.-47G>A
NM_001282512.1:c.242G>A	NP_001269441.1:p.Gly81Asp
NM_006440.4:c.242G>A	NP_006431.2:p.Gly81Asp
NM_001282512.2:c.242G>A	NP_001269441.1:p.Gly81Asp
NM_001352300.1:c.239G>A	NP_001339229.1:p.Gly80Asp
NM_001352301.1:c.152G>A	NP_001339230.1:p.Gly51Asp
NM_001352302.1:c.-47G>A	NP_001339231.1:n.-47G>A
NM_001352303.1:c.146G>A	NP_001339232.1:p.Gly49Asp
NR_147957.1:n.374G>A
NM_006440.5:c.242G>A MANE Select	NP_006431.2:p.Gly81Asp
NM_001282512.3:c.242G>A	NP_001269441.1:p.Gly81Asp
NM_001352300.2:c.239G>A	NP_001339229.1:p.Gly80Asp
NR_147957.2:n.200G>A
NM_001352301.2:c.152G>A	NP_001339230.1:p.Gly51Asp
NM_001352302.2:c.-47G>A	NP_001339231.1:n.-47G>A
NM_001352303.2:c.146G>A	NP_001339232.1:p.Gly49Asp