Canonical Allele Identifier: CA410686525

Gene: TXNRD2

Linked Data

• gnomAD v4: 22-19895458-T-C
• MyVariant Identifiers: chr22:g.19882981T>C (hg19) ; chr22:g.19895458T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895458T>C , CM000684.2:g.19895458T>C	GRCh38
NC_000022.10:g.19882981T>C , CM000684.1:g.19882981T>C	GRCh37
NC_000022.9:g.18262981T>C	NCBI36
NG_011835.1:g.51379A>G , LRG_417:g.51379A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.898A>G MANE Select	ENSP00000383365.1:p.Thr300Ala
ENST00000334363.14:c.898A>G	ENSP00000334451.9:p.Thr300Ala
ENST00000400518.5:c.808A>G	ENSP00000383362.1:p.Thr270Ala
ENST00000400519.6:c.895A>G	ENSP00000383363.1:p.Thr299Ala
ENST00000400521.6:c.898A>G	ENSP00000383365.1:p.Thr300Ala
ENST00000400525.6:c.829A>G	ENSP00000383369.3:p.Thr277Ala
ENST00000474308.5:c.841A>G	ENSP00000485665.1:p.Thr281Ala
ENST00000475995.3:c.395A>G
ENST00000491939.6:c.802A>G	ENSP00000485543.1:p.Thr268Ala
ENST00000494454.5:n.972A>G
ENST00000542719.6:c.610A>G	ENSP00000485128.2:p.Thr204Ala
ENST00000634537.1:c.127A>G	ENSP00000489208.1:p.Thr43Ala
ENST00000635155.1:n.484A>G
NM_001282512.1:c.898A>G	NP_001269441.1:p.Thr300Ala
NM_006440.4:c.898A>G	NP_006431.2:p.Thr300Ala
NM_001282512.2:c.898A>G	NP_001269441.1:p.Thr300Ala
NM_001352300.1:c.895A>G	NP_001339229.1:p.Thr299Ala
NM_001352301.1:c.808A>G	NP_001339230.1:p.Thr270Ala
NM_001352302.1:c.610A>G	NP_001339231.1:p.Thr204Ala
NM_001352303.1:c.802A>G	NP_001339232.1:p.Thr268Ala
NR_147957.1:n.1030A>G
NM_006440.5:c.898A>G MANE Select	NP_006431.2:p.Thr300Ala
NM_001282512.3:c.898A>G	NP_001269441.1:p.Thr300Ala
NM_001352300.2:c.895A>G	NP_001339229.1:p.Thr299Ala
NR_147957.2:n.856A>G
NM_001352301.2:c.808A>G	NP_001339230.1:p.Thr270Ala
NM_001352302.2:c.610A>G	NP_001339231.1:p.Thr204Ala
NM_001352303.2:c.802A>G	NP_001339232.1:p.Thr268Ala