Canonical Allele Identifier: CA410693843

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19906449A>C (hg19) ; chr22:g.19918926A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918926A>C , CM000684.2:g.19918926A>C	GRCh38
NC_000022.10:g.19906449A>C , CM000684.1:g.19906449A>C	GRCh37
NC_000022.9:g.18286449A>C	NCBI36
NG_011835.1:g.27911T>G , LRG_417:g.27911T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.308T>G MANE Select	ENSP00000383365.1:p.Leu103Arg
ENST00000334363.14:c.308T>G	ENSP00000334451.9:p.Leu103Arg
ENST00000400518.5:c.218T>G	ENSP00000383362.1:p.Leu73Arg
ENST00000400519.6:c.305T>G	ENSP00000383363.1:p.Leu102Arg
ENST00000400521.6:c.308T>G	ENSP00000383365.1:p.Leu103Arg
ENST00000400525.6:c.239T>G	ENSP00000383369.3:p.Leu80Arg
ENST00000474308.5:c.251T>G	ENSP00000485665.1:p.Leu84Arg
ENST00000491939.6:c.212T>G	ENSP00000485543.1:p.Leu71Arg
ENST00000496729.2:n.313T>G
ENST00000542719.6:c.20T>G	ENSP00000485128.2:p.Leu7Arg
NM_001282512.1:c.308T>G	NP_001269441.1:p.Leu103Arg
NM_006440.4:c.308T>G	NP_006431.2:p.Leu103Arg
NM_001282512.2:c.308T>G	NP_001269441.1:p.Leu103Arg
NM_001352300.1:c.305T>G	NP_001339229.1:p.Leu102Arg
NM_001352301.1:c.218T>G	NP_001339230.1:p.Leu73Arg
NM_001352302.1:c.20T>G	NP_001339231.1:p.Leu7Arg
NM_001352303.1:c.212T>G	NP_001339232.1:p.Leu71Arg
NR_147957.1:n.440T>G
NM_006440.5:c.308T>G MANE Select	NP_006431.2:p.Leu103Arg
NM_001282512.3:c.308T>G	NP_001269441.1:p.Leu103Arg
NM_001352300.2:c.305T>G	NP_001339229.1:p.Leu102Arg
NR_147957.2:n.266T>G
NM_001352301.2:c.218T>G	NP_001339230.1:p.Leu73Arg
NM_001352302.2:c.20T>G	NP_001339231.1:p.Leu7Arg
NM_001352303.2:c.212T>G	NP_001339232.1:p.Leu71Arg