Canonical Allele Identifier: CA410686392

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19882956G>C (hg19) ; chr22:g.19895433G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895433G>C , CM000684.2:g.19895433G>C	GRCh38
NC_000022.10:g.19882956G>C , CM000684.1:g.19882956G>C	GRCh37
NC_000022.9:g.18262956G>C	NCBI36
NG_011835.1:g.51404C>G , LRG_417:g.51404C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.923C>G MANE Select	ENSP00000383365.1:p.Thr308Ser
ENST00000334363.14:c.923C>G	ENSP00000334451.9:p.Thr308Ser
ENST00000400518.5:c.833C>G	ENSP00000383362.1:p.Thr278Ser
ENST00000400519.6:c.920C>G	ENSP00000383363.1:p.Thr307Ser
ENST00000400521.6:c.923C>G	ENSP00000383365.1:p.Thr308Ser
ENST00000400525.6:c.854C>G	ENSP00000383369.3:p.Thr285Ser
ENST00000474308.5:c.866C>G	ENSP00000485665.1:p.Thr289Ser
ENST00000475995.3:c.420C>G
ENST00000491939.6:c.827C>G	ENSP00000485543.1:p.Thr276Ser
ENST00000494454.5:n.997C>G
ENST00000542719.6:c.635C>G	ENSP00000485128.2:p.Thr212Ser
ENST00000634537.1:c.152C>G	ENSP00000489208.1:p.Thr51Ser
ENST00000635155.1:n.509C>G
NM_001282512.1:c.923C>G	NP_001269441.1:p.Thr308Ser
NM_006440.4:c.923C>G	NP_006431.2:p.Thr308Ser
NM_001282512.2:c.923C>G	NP_001269441.1:p.Thr308Ser
NM_001352300.1:c.920C>G	NP_001339229.1:p.Thr307Ser
NM_001352301.1:c.833C>G	NP_001339230.1:p.Thr278Ser
NM_001352302.1:c.635C>G	NP_001339231.1:p.Thr212Ser
NM_001352303.1:c.827C>G	NP_001339232.1:p.Thr276Ser
NR_147957.1:n.1055C>G
NM_006440.5:c.923C>G MANE Select	NP_006431.2:p.Thr308Ser
NM_001282512.3:c.923C>G	NP_001269441.1:p.Thr308Ser
NM_001352300.2:c.920C>G	NP_001339229.1:p.Thr307Ser
NR_147957.2:n.881C>G
NM_001352301.2:c.833C>G	NP_001339230.1:p.Thr278Ser
NM_001352302.2:c.635C>G	NP_001339231.1:p.Thr212Ser
NM_001352303.2:c.827C>G	NP_001339232.1:p.Thr276Ser