Canonical Allele Identifier: CA513365184

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19883000C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895477C>T , CM000684.2:g.19895477C>T	GRCh38
NC_000022.10:g.19883000C>T , CM000684.1:g.19883000C>T	GRCh37
NC_000022.9:g.18263000C>T	NCBI36
NG_011835.1:g.51360G>A , LRG_417:g.51360G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.879G>A MANE Select	ENSP00000383365.1:p.Gln293=
ENST00000334363.14:c.879G>A	ENSP00000334451.9:p.Gln293=
ENST00000400518.5:c.789G>A	ENSP00000383362.1:p.Gln263=
ENST00000400519.6:c.876G>A	ENSP00000383363.1:p.Gln292=
ENST00000400521.6:c.879G>A	ENSP00000383365.1:p.Gln293=
ENST00000400525.6:c.810G>A	ENSP00000383369.3:p.Gln270=
ENST00000474308.5:c.822G>A	ENSP00000485665.1:p.Gln274=
ENST00000475995.3:c.376G>A
ENST00000491939.6:c.783G>A	ENSP00000485543.1:p.Gln261=
ENST00000494454.5:n.953G>A
ENST00000542719.6:c.591G>A	ENSP00000485128.2:p.Gln197=
ENST00000634537.1:c.108G>A	ENSP00000489208.1:p.Gln36=
ENST00000635155.1:n.465G>A
NM_001282512.1:c.879G>A	NP_001269441.1:p.Gln293=
NM_006440.4:c.879G>A	NP_006431.2:p.Gln293=
NM_001282512.2:c.879G>A	NP_001269441.1:p.Gln293=
NM_001352300.1:c.876G>A	NP_001339229.1:p.Gln292=
NM_001352301.1:c.789G>A	NP_001339230.1:p.Gln263=
NM_001352302.1:c.591G>A	NP_001339231.1:p.Gln197=
NM_001352303.1:c.783G>A	NP_001339232.1:p.Gln261=
NR_147957.1:n.1011G>A
NM_006440.5:c.879G>A MANE Select	NP_006431.2:p.Gln293=
NM_001282512.3:c.879G>A	NP_001269441.1:p.Gln293=
NM_001352300.2:c.876G>A	NP_001339229.1:p.Gln292=
NR_147957.2:n.837G>A
NM_001352301.2:c.789G>A	NP_001339230.1:p.Gln263=
NM_001352302.2:c.591G>A	NP_001339231.1:p.Gln197=
NM_001352303.2:c.783G>A	NP_001339232.1:p.Gln261=