Canonical Allele Identifier: CA322105577

Gene: TXNRD2

Linked Data

• dbSNP Id: rs896720951
• MyVariant Identifiers: chr22:g.19906455G>T (hg19) ; chr22:g.19918932G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918932G>T , CM000684.2:g.19918932G>T	GRCh38
NC_000022.10:g.19906455G>T , CM000684.1:g.19906455G>T	GRCh37
NC_000022.9:g.18286455G>T	NCBI36
NG_011835.1:g.27905C>A , LRG_417:g.27905C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.302C>A MANE Select	ENSP00000383365.1:p.Ala101Glu
ENST00000334363.14:c.302C>A	ENSP00000334451.9:p.Ala101Glu
ENST00000400518.5:c.212C>A	ENSP00000383362.1:p.Ala71Glu
ENST00000400519.6:c.299C>A	ENSP00000383363.1:p.Ala100Glu
ENST00000400521.6:c.302C>A	ENSP00000383365.1:p.Ala101Glu
ENST00000400525.6:c.233C>A	ENSP00000383369.3:p.Ala78Glu
ENST00000474308.5:c.245C>A	ENSP00000485665.1:p.Ala82Glu
ENST00000491939.6:c.206C>A	ENSP00000485543.1:p.Ala69Glu
ENST00000496729.2:n.307C>A
ENST00000542719.6:c.14C>A	ENSP00000485128.2:p.Ala5Glu
NM_001282512.1:c.302C>A	NP_001269441.1:p.Ala101Glu
NM_006440.4:c.302C>A	NP_006431.2:p.Ala101Glu
NM_001282512.2:c.302C>A	NP_001269441.1:p.Ala101Glu
NM_001352300.1:c.299C>A	NP_001339229.1:p.Ala100Glu
NM_001352301.1:c.212C>A	NP_001339230.1:p.Ala71Glu
NM_001352302.1:c.14C>A	NP_001339231.1:p.Ala5Glu
NM_001352303.1:c.206C>A	NP_001339232.1:p.Ala69Glu
NR_147957.1:n.434C>A
NM_006440.5:c.302C>A MANE Select	NP_006431.2:p.Ala101Glu
NM_001282512.3:c.302C>A	NP_001269441.1:p.Ala101Glu
NM_001352300.2:c.299C>A	NP_001339229.1:p.Ala100Glu
NR_147957.2:n.260C>A
NM_001352301.2:c.212C>A	NP_001339230.1:p.Ala71Glu
NM_001352302.2:c.14C>A	NP_001339231.1:p.Ala5Glu
NM_001352303.2:c.206C>A	NP_001339232.1:p.Ala69Glu