Canonical Allele Identifier: CA513365261

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19883027G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895504G>T , CM000684.2:g.19895504G>T	GRCh38
NC_000022.10:g.19883027G>T , CM000684.1:g.19883027G>T	GRCh37
NC_000022.9:g.18263027G>T	NCBI36
NG_011835.1:g.51333C>A , LRG_417:g.51333C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.852C>A MANE Select	ENSP00000383365.1:p.Val284=
ENST00000334363.14:c.852C>A	ENSP00000334451.9:p.Val284=
ENST00000400518.5:c.762C>A	ENSP00000383362.1:p.Val254=
ENST00000400519.6:c.849C>A	ENSP00000383363.1:p.Val283=
ENST00000400521.6:c.852C>A	ENSP00000383365.1:p.Val284=
ENST00000400525.6:c.783C>A	ENSP00000383369.3:p.Val261=
ENST00000474308.5:c.795C>A	ENSP00000485665.1:p.Val265=
ENST00000475995.3:c.349C>A
ENST00000491939.6:c.756C>A	ENSP00000485543.1:p.Val252=
ENST00000494454.5:n.926C>A
ENST00000542719.6:c.564C>A	ENSP00000485128.2:p.Val188=
ENST00000634537.1:c.81C>A	ENSP00000489208.1:p.Val27=
ENST00000635155.1:n.438C>A
NM_001282512.1:c.852C>A	NP_001269441.1:p.Val284=
NM_006440.4:c.852C>A	NP_006431.2:p.Val284=
NM_001282512.2:c.852C>A	NP_001269441.1:p.Val284=
NM_001352300.1:c.849C>A	NP_001339229.1:p.Val283=
NM_001352301.1:c.762C>A	NP_001339230.1:p.Val254=
NM_001352302.1:c.564C>A	NP_001339231.1:p.Val188=
NM_001352303.1:c.756C>A	NP_001339232.1:p.Val252=
NR_147957.1:n.984C>A
NM_006440.5:c.852C>A MANE Select	NP_006431.2:p.Val284=
NM_001282512.3:c.852C>A	NP_001269441.1:p.Val284=
NM_001352300.2:c.849C>A	NP_001339229.1:p.Val283=
NR_147957.2:n.810C>A
NM_001352301.2:c.762C>A	NP_001339230.1:p.Val254=
NM_001352302.2:c.564C>A	NP_001339231.1:p.Val188=
NM_001352303.2:c.756C>A	NP_001339232.1:p.Val252=