Canonical Allele Identifier: CA410693957

Gene: TXNRD2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.275T>G MANE Select	ENSP00000383365.1:p.Ile92Ser
ENST00000334363.14:c.275T>G	ENSP00000334451.9:p.Ile92Ser
ENST00000400518.5:c.185T>G	ENSP00000383362.1:p.Ile62Ser
ENST00000400519.6:c.272T>G	ENSP00000383363.1:p.Ile91Ser
ENST00000400521.6:c.275T>G	ENSP00000383365.1:p.Ile92Ser
ENST00000400525.6:c.206T>G	ENSP00000383369.3:p.Ile69Ser
ENST00000474308.5:c.218T>G	ENSP00000485665.1:p.Ile73Ser
ENST00000491939.6:c.179T>G	ENSP00000485543.1:p.Ile60Ser
ENST00000496729.2:n.280T>G
ENST00000542719.6:c.-14T>G	ENSP00000485128.2:n.-14T>G
NM_001282512.1:c.275T>G	NP_001269441.1:p.Ile92Ser
NM_006440.4:c.275T>G	NP_006431.2:p.Ile92Ser
NM_001282512.2:c.275T>G	NP_001269441.1:p.Ile92Ser
NM_001352300.1:c.272T>G	NP_001339229.1:p.Ile91Ser
NM_001352301.1:c.185T>G	NP_001339230.1:p.Ile62Ser
NM_001352302.1:c.-14T>G	NP_001339231.1:n.-14T>G
NM_001352303.1:c.179T>G	NP_001339232.1:p.Ile60Ser
NR_147957.1:n.407T>G
NM_006440.5:c.275T>G MANE Select	NP_006431.2:p.Ile92Ser
NM_001282512.3:c.275T>G	NP_001269441.1:p.Ile92Ser
NM_001352300.2:c.272T>G	NP_001339229.1:p.Ile91Ser
NR_147957.2:n.233T>G
NM_001352301.2:c.185T>G	NP_001339230.1:p.Ile62Ser
NM_001352302.2:c.-14T>G	NP_001339231.1:n.-14T>G
NM_001352303.2:c.179T>G	NP_001339232.1:p.Ile60Ser