Canonical Allele Identifier: CA410693922

Gene: TXNRD2

Linked Data

• gnomAD v4: 22-19918948-G-T
• MyVariant Identifiers: chr22:g.19906471G>T (hg19) ; chr22:g.19918948G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918948G>T , CM000684.2:g.19918948G>T	GRCh38
NC_000022.10:g.19906471G>T , CM000684.1:g.19906471G>T	GRCh37
NC_000022.9:g.18286471G>T	NCBI36
NG_011835.1:g.27889C>A , LRG_417:g.27889C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.286C>A MANE Select	ENSP00000383365.1:p.Leu96Met
ENST00000334363.14:c.286C>A	ENSP00000334451.9:p.Leu96Met
ENST00000400518.5:c.196C>A	ENSP00000383362.1:p.Leu66Met
ENST00000400519.6:c.283C>A	ENSP00000383363.1:p.Leu95Met
ENST00000400521.6:c.286C>A	ENSP00000383365.1:p.Leu96Met
ENST00000400525.6:c.217C>A	ENSP00000383369.3:p.Leu73Met
ENST00000474308.5:c.229C>A	ENSP00000485665.1:p.Leu77Met
ENST00000491939.6:c.190C>A	ENSP00000485543.1:p.Leu64Met
ENST00000496729.2:n.291C>A
ENST00000542719.6:c.-3C>A	ENSP00000485128.2:n.-3C>A
NM_001282512.1:c.286C>A	NP_001269441.1:p.Leu96Met
NM_006440.4:c.286C>A	NP_006431.2:p.Leu96Met
NM_001282512.2:c.286C>A	NP_001269441.1:p.Leu96Met
NM_001352300.1:c.283C>A	NP_001339229.1:p.Leu95Met
NM_001352301.1:c.196C>A	NP_001339230.1:p.Leu66Met
NM_001352302.1:c.-3C>A	NP_001339231.1:n.-3C>A
NM_001352303.1:c.190C>A	NP_001339232.1:p.Leu64Met
NR_147957.1:n.418C>A
NM_006440.5:c.286C>A MANE Select	NP_006431.2:p.Leu96Met
NM_001282512.3:c.286C>A	NP_001269441.1:p.Leu96Met
NM_001352300.2:c.283C>A	NP_001339229.1:p.Leu95Met
NR_147957.2:n.244C>A
NM_001352301.2:c.196C>A	NP_001339230.1:p.Leu66Met
NM_001352302.2:c.-3C>A	NP_001339231.1:n.-3C>A
NM_001352303.2:c.190C>A	NP_001339232.1:p.Leu64Met