Canonical Allele Identifier: CA410693959

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19906482A>T (hg19) ; chr22:g.19918959A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918959A>T , CM000684.2:g.19918959A>T	GRCh38
NC_000022.10:g.19906482A>T , CM000684.1:g.19906482A>T	GRCh37
NC_000022.9:g.18286482A>T	NCBI36
NG_011835.1:g.27878T>A , LRG_417:g.27878T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.275T>A MANE Select	ENSP00000383365.1:p.Ile92Asn
ENST00000334363.14:c.275T>A	ENSP00000334451.9:p.Ile92Asn
ENST00000400518.5:c.185T>A	ENSP00000383362.1:p.Ile62Asn
ENST00000400519.6:c.272T>A	ENSP00000383363.1:p.Ile91Asn
ENST00000400521.6:c.275T>A	ENSP00000383365.1:p.Ile92Asn
ENST00000400525.6:c.206T>A	ENSP00000383369.3:p.Ile69Asn
ENST00000474308.5:c.218T>A	ENSP00000485665.1:p.Ile73Asn
ENST00000491939.6:c.179T>A	ENSP00000485543.1:p.Ile60Asn
ENST00000496729.2:n.280T>A
ENST00000542719.6:c.-14T>A	ENSP00000485128.2:n.-14T>A
NM_001282512.1:c.275T>A	NP_001269441.1:p.Ile92Asn
NM_006440.4:c.275T>A	NP_006431.2:p.Ile92Asn
NM_001282512.2:c.275T>A	NP_001269441.1:p.Ile92Asn
NM_001352300.1:c.272T>A	NP_001339229.1:p.Ile91Asn
NM_001352301.1:c.185T>A	NP_001339230.1:p.Ile62Asn
NM_001352302.1:c.-14T>A	NP_001339231.1:n.-14T>A
NM_001352303.1:c.179T>A	NP_001339232.1:p.Ile60Asn
NR_147957.1:n.407T>A
NM_006440.5:c.275T>A MANE Select	NP_006431.2:p.Ile92Asn
NM_001282512.3:c.275T>A	NP_001269441.1:p.Ile92Asn
NM_001352300.2:c.272T>A	NP_001339229.1:p.Ile91Asn
NR_147957.2:n.233T>A
NM_001352301.2:c.185T>A	NP_001339230.1:p.Ile62Asn
NM_001352302.2:c.-14T>A	NP_001339231.1:n.-14T>A
NM_001352303.2:c.179T>A	NP_001339232.1:p.Ile60Asn