Canonical Allele Identifier: CA513369052

Gene: TXNRD2

Linked Data

• gnomAD v4: 22-19918892-G-T
• MyVariant Identifiers: chr22:g.19906415G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918892G>T , CM000684.2:g.19918892G>T	GRCh38
NC_000022.10:g.19906415G>T , CM000684.1:g.19906415G>T	GRCh37
NC_000022.9:g.18286415G>T	NCBI36
NG_011835.1:g.27945C>A , LRG_417:g.27945C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.342C>A MANE Select	ENSP00000383365.1:p.Gly114=
ENST00000334363.14:c.342C>A	ENSP00000334451.9:p.Gly114=
ENST00000400518.5:c.252C>A	ENSP00000383362.1:p.Gly84=
ENST00000400519.6:c.339C>A	ENSP00000383363.1:p.Gly113=
ENST00000400521.6:c.342C>A	ENSP00000383365.1:p.Gly114=
ENST00000400525.6:c.273C>A	ENSP00000383369.3:p.Gly91=
ENST00000474308.5:c.285C>A	ENSP00000485665.1:p.Gly95=
ENST00000491939.6:c.246C>A	ENSP00000485543.1:p.Gly82=
ENST00000496729.2:n.347C>A
ENST00000542719.6:c.54C>A	ENSP00000485128.2:p.Gly18=
NM_001282512.1:c.342C>A	NP_001269441.1:p.Gly114=
NM_006440.4:c.342C>A	NP_006431.2:p.Gly114=
NM_001282512.2:c.342C>A	NP_001269441.1:p.Gly114=
NM_001352300.1:c.339C>A	NP_001339229.1:p.Gly113=
NM_001352301.1:c.252C>A	NP_001339230.1:p.Gly84=
NM_001352302.1:c.54C>A	NP_001339231.1:p.Gly18=
NM_001352303.1:c.246C>A	NP_001339232.1:p.Gly82=
NR_147957.1:n.474C>A
NM_006440.5:c.342C>A MANE Select	NP_006431.2:p.Gly114=
NM_001282512.3:c.342C>A	NP_001269441.1:p.Gly114=
NM_001352300.2:c.339C>A	NP_001339229.1:p.Gly113=
NR_147957.2:n.300C>A
NM_001352301.2:c.252C>A	NP_001339230.1:p.Gly84=
NM_001352302.2:c.54C>A	NP_001339231.1:p.Gly18=
NM_001352303.2:c.246C>A	NP_001339232.1:p.Gly82=