Canonical Allele Identifier: CA410686799

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19883104G>C (hg19) ; chr22:g.19895581G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895581G>C , CM000684.2:g.19895581G>C	GRCh38
NC_000022.10:g.19883104G>C , CM000684.1:g.19883104G>C	GRCh37
NC_000022.9:g.18263104G>C	NCBI36
NG_011835.1:g.51256C>G , LRG_417:g.51256C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.775C>G MANE Select	ENSP00000383365.1:p.Gln259Glu
ENST00000334363.14:c.775C>G	ENSP00000334451.9:p.Gln259Glu
ENST00000400518.5:c.685C>G	ENSP00000383362.1:p.Gln229Glu
ENST00000400519.6:c.772C>G	ENSP00000383363.1:p.Gln258Glu
ENST00000400521.6:c.775C>G	ENSP00000383365.1:p.Gln259Glu
ENST00000400525.6:c.706C>G	ENSP00000383369.3:p.Gln236Glu
ENST00000474308.5:c.718C>G	ENSP00000485665.1:p.Gln240Glu
ENST00000475995.3:c.272C>G
ENST00000491939.6:c.679C>G	ENSP00000485543.1:p.Gln227Glu
ENST00000494454.5:n.849C>G
ENST00000542719.6:c.487C>G	ENSP00000485128.2:p.Gln163Glu
ENST00000634537.1:c.4C>G	ENSP00000489208.1:p.Gln2Glu
ENST00000635155.1:n.361C>G
NM_001282512.1:c.775C>G	NP_001269441.1:p.Gln259Glu
NM_006440.4:c.775C>G	NP_006431.2:p.Gln259Glu
NM_001282512.2:c.775C>G	NP_001269441.1:p.Gln259Glu
NM_001352300.1:c.772C>G	NP_001339229.1:p.Gln258Glu
NM_001352301.1:c.685C>G	NP_001339230.1:p.Gln229Glu
NM_001352302.1:c.487C>G	NP_001339231.1:p.Gln163Glu
NM_001352303.1:c.679C>G	NP_001339232.1:p.Gln227Glu
NR_147957.1:n.907C>G
NM_006440.5:c.775C>G MANE Select	NP_006431.2:p.Gln259Glu
NM_001282512.3:c.775C>G	NP_001269441.1:p.Gln259Glu
NM_001352300.2:c.772C>G	NP_001339229.1:p.Gln258Glu
NR_147957.2:n.733C>G
NM_001352301.2:c.685C>G	NP_001339230.1:p.Gln229Glu
NM_001352302.2:c.487C>G	NP_001339231.1:p.Gln163Glu
NM_001352303.2:c.679C>G	NP_001339232.1:p.Gln227Glu