Canonical Allele Identifier: CA513365141

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19882934G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895411G>T , CM000684.2:g.19895411G>T	GRCh38
NC_000022.10:g.19882934G>T , CM000684.1:g.19882934G>T	GRCh37
NC_000022.9:g.18262934G>T	NCBI36
NG_011835.1:g.51426C>A , LRG_417:g.51426C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.945C>A MANE Select	ENSP00000383365.1:p.Ala315=
ENST00000334363.14:c.945C>A	ENSP00000334451.9:p.Ala315=
ENST00000400518.5:c.855C>A	ENSP00000383362.1:p.Ala285=
ENST00000400519.6:c.942C>A	ENSP00000383363.1:p.Ala314=
ENST00000400521.6:c.945C>A	ENSP00000383365.1:p.Ala315=
ENST00000400525.6:c.876C>A	ENSP00000383369.3:p.Ala292=
ENST00000474308.5:c.888C>A	ENSP00000485665.1:p.Ala296=
ENST00000475995.3:c.442C>A
ENST00000491939.6:c.849C>A	ENSP00000485543.1:p.Ala283=
ENST00000494454.5:n.1019C>A
ENST00000542719.6:c.657C>A	ENSP00000485128.2:p.Ala219=
ENST00000634537.1:c.174C>A	ENSP00000489208.1:p.Ala58=
ENST00000635155.1:n.531C>A
NM_001282512.1:c.945C>A	NP_001269441.1:p.Ala315=
NM_006440.4:c.945C>A	NP_006431.2:p.Ala315=
NM_001282512.2:c.945C>A	NP_001269441.1:p.Ala315=
NM_001352300.1:c.942C>A	NP_001339229.1:p.Ala314=
NM_001352301.1:c.855C>A	NP_001339230.1:p.Ala285=
NM_001352302.1:c.657C>A	NP_001339231.1:p.Ala219=
NM_001352303.1:c.849C>A	NP_001339232.1:p.Ala283=
NR_147957.1:n.1077C>A
NM_006440.5:c.945C>A MANE Select	NP_006431.2:p.Ala315=
NM_001282512.3:c.945C>A	NP_001269441.1:p.Ala315=
NM_001352300.2:c.942C>A	NP_001339229.1:p.Ala314=
NR_147957.2:n.903C>A
NM_001352301.2:c.855C>A	NP_001339230.1:p.Ala285=
NM_001352302.2:c.657C>A	NP_001339231.1:p.Ala219=
NM_001352303.2:c.849C>A	NP_001339232.1:p.Ala283=