Canonical Allele Identifier: CA410686601

Gene: TXNRD2

Linked Data

• dbSNP Id: rs1939462859
• gnomAD v3: 22-19895485-G-A
• gnomAD v4: 22-19895485-G-A
• MyVariant Identifiers: chr22:g.19883008G>A (hg19) ; chr22:g.19895485G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895485G>A , CM000684.2:g.19895485G>A	GRCh38
NC_000022.10:g.19883008G>A , CM000684.1:g.19883008G>A	GRCh37
NC_000022.9:g.18263008G>A	NCBI36
NG_011835.1:g.51352C>T , LRG_417:g.51352C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.871C>T MANE Select	ENSP00000383365.1:p.Gln291Ter
ENST00000334363.14:c.871C>T	ENSP00000334451.9:p.Gln291Ter
ENST00000400518.5:c.781C>T	ENSP00000383362.1:p.Gln261Ter
ENST00000400519.6:c.868C>T	ENSP00000383363.1:p.Gln290Ter
ENST00000400521.6:c.871C>T	ENSP00000383365.1:p.Gln291Ter
ENST00000400525.6:c.802C>T	ENSP00000383369.3:p.Gln268Ter
ENST00000474308.5:c.814C>T	ENSP00000485665.1:p.Gln272Ter
ENST00000475995.3:c.368C>T
ENST00000491939.6:c.775C>T	ENSP00000485543.1:p.Gln259Ter
ENST00000494454.5:n.945C>T
ENST00000542719.6:c.583C>T	ENSP00000485128.2:p.Gln195Ter
ENST00000634537.1:c.100C>T	ENSP00000489208.1:p.Gln34Ter
ENST00000635155.1:n.457C>T
NM_001282512.1:c.871C>T	NP_001269441.1:p.Gln291Ter
NM_006440.4:c.871C>T	NP_006431.2:p.Gln291Ter
NM_001282512.2:c.871C>T	NP_001269441.1:p.Gln291Ter
NM_001352300.1:c.868C>T	NP_001339229.1:p.Gln290Ter
NM_001352301.1:c.781C>T	NP_001339230.1:p.Gln261Ter
NM_001352302.1:c.583C>T	NP_001339231.1:p.Gln195Ter
NM_001352303.1:c.775C>T	NP_001339232.1:p.Gln259Ter
NR_147957.1:n.1003C>T
NM_006440.5:c.871C>T MANE Select	NP_006431.2:p.Gln291Ter
NM_001282512.3:c.871C>T	NP_001269441.1:p.Gln291Ter
NM_001352300.2:c.868C>T	NP_001339229.1:p.Gln290Ter
NR_147957.2:n.829C>T
NM_001352301.2:c.781C>T	NP_001339230.1:p.Gln261Ter
NM_001352302.2:c.583C>T	NP_001339231.1:p.Gln195Ter
NM_001352303.2:c.775C>T	NP_001339232.1:p.Gln259Ter