Canonical Allele Identifier: CA410693661

Gene: TXNRD2

Linked Data

• gnomAD v4: 22-19918875-G-T
• MyVariant Identifiers: chr22:g.19906398G>T (hg19) ; chr22:g.19918875G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918875G>T , CM000684.2:g.19918875G>T	GRCh38
NC_000022.10:g.19906398G>T , CM000684.1:g.19906398G>T	GRCh37
NC_000022.9:g.18286398G>T	NCBI36
NG_011835.1:g.27962C>A , LRG_417:g.27962C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.359C>A MANE Select	ENSP00000383365.1:p.Pro120His
ENST00000334363.14:c.359C>A	ENSP00000334451.9:p.Pro120His
ENST00000400518.5:c.269C>A	ENSP00000383362.1:p.Pro90His
ENST00000400519.6:c.356C>A	ENSP00000383363.1:p.Pro119His
ENST00000400521.6:c.359C>A	ENSP00000383365.1:p.Pro120His
ENST00000400525.6:c.290C>A	ENSP00000383369.3:p.Pro97His
ENST00000474308.5:c.302C>A	ENSP00000485665.1:p.Pro101His
ENST00000491939.6:c.263C>A	ENSP00000485543.1:p.Pro88His
ENST00000496729.2:n.364C>A
ENST00000542719.6:c.71C>A	ENSP00000485128.2:p.Pro24His
NM_001282512.1:c.359C>A	NP_001269441.1:p.Pro120His
NM_006440.4:c.359C>A	NP_006431.2:p.Pro120His
NM_001282512.2:c.359C>A	NP_001269441.1:p.Pro120His
NM_001352300.1:c.356C>A	NP_001339229.1:p.Pro119His
NM_001352301.1:c.269C>A	NP_001339230.1:p.Pro90His
NM_001352302.1:c.71C>A	NP_001339231.1:p.Pro24His
NM_001352303.1:c.263C>A	NP_001339232.1:p.Pro88His
NR_147957.1:n.491C>A
NM_006440.5:c.359C>A MANE Select	NP_006431.2:p.Pro120His
NM_001282512.3:c.359C>A	NP_001269441.1:p.Pro120His
NM_001352300.2:c.356C>A	NP_001339229.1:p.Pro119His
NR_147957.2:n.317C>A
NM_001352301.2:c.269C>A	NP_001339230.1:p.Pro90His
NM_001352302.2:c.71C>A	NP_001339231.1:p.Pro24His
NM_001352303.2:c.263C>A	NP_001339232.1:p.Pro88His