Canonical Allele Identifier: CA410693888

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19906462G>C (hg19) ; chr22:g.19918939G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918939G>C , CM000684.2:g.19918939G>C	GRCh38
NC_000022.10:g.19906462G>C , CM000684.1:g.19906462G>C	GRCh37
NC_000022.9:g.18286462G>C	NCBI36
NG_011835.1:g.27898C>G , LRG_417:g.27898C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.295C>G MANE Select	ENSP00000383365.1:p.Gln99Glu
ENST00000334363.14:c.295C>G	ENSP00000334451.9:p.Gln99Glu
ENST00000400518.5:c.205C>G	ENSP00000383362.1:p.Gln69Glu
ENST00000400519.6:c.292C>G	ENSP00000383363.1:p.Gln98Glu
ENST00000400521.6:c.295C>G	ENSP00000383365.1:p.Gln99Glu
ENST00000400525.6:c.226C>G	ENSP00000383369.3:p.Gln76Glu
ENST00000474308.5:c.238C>G	ENSP00000485665.1:p.Gln80Glu
ENST00000491939.6:c.199C>G	ENSP00000485543.1:p.Gln67Glu
ENST00000496729.2:n.300C>G
ENST00000542719.6:c.7C>G	ENSP00000485128.2:p.Gln3Glu
NM_001282512.1:c.295C>G	NP_001269441.1:p.Gln99Glu
NM_006440.4:c.295C>G	NP_006431.2:p.Gln99Glu
NM_001282512.2:c.295C>G	NP_001269441.1:p.Gln99Glu
NM_001352300.1:c.292C>G	NP_001339229.1:p.Gln98Glu
NM_001352301.1:c.205C>G	NP_001339230.1:p.Gln69Glu
NM_001352302.1:c.7C>G	NP_001339231.1:p.Gln3Glu
NM_001352303.1:c.199C>G	NP_001339232.1:p.Gln67Glu
NR_147957.1:n.427C>G
NM_006440.5:c.295C>G MANE Select	NP_006431.2:p.Gln99Glu
NM_001282512.3:c.295C>G	NP_001269441.1:p.Gln99Glu
NM_001352300.2:c.292C>G	NP_001339229.1:p.Gln98Glu
NR_147957.2:n.253C>G
NM_001352301.2:c.205C>G	NP_001339230.1:p.Gln69Glu
NM_001352302.2:c.7C>G	NP_001339231.1:p.Gln3Glu
NM_001352303.2:c.199C>G	NP_001339232.1:p.Gln67Glu