Canonical Allele Identifier: CA513365174

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19882994G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895471G>T , CM000684.2:g.19895471G>T	GRCh38
NC_000022.10:g.19882994G>T , CM000684.1:g.19882994G>T	GRCh37
NC_000022.9:g.18262994G>T	NCBI36
NG_011835.1:g.51366C>A , LRG_417:g.51366C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.885C>A MANE Select	ENSP00000383365.1:p.Thr295=
ENST00000334363.14:c.885C>A	ENSP00000334451.9:p.Thr295=
ENST00000400518.5:c.795C>A	ENSP00000383362.1:p.Thr265=
ENST00000400519.6:c.882C>A	ENSP00000383363.1:p.Thr294=
ENST00000400521.6:c.885C>A	ENSP00000383365.1:p.Thr295=
ENST00000400525.6:c.816C>A	ENSP00000383369.3:p.Thr272=
ENST00000474308.5:c.828C>A	ENSP00000485665.1:p.Thr276=
ENST00000475995.3:c.382C>A
ENST00000491939.6:c.789C>A	ENSP00000485543.1:p.Thr263=
ENST00000494454.5:n.959C>A
ENST00000542719.6:c.597C>A	ENSP00000485128.2:p.Thr199=
ENST00000634537.1:c.114C>A	ENSP00000489208.1:p.Thr38=
ENST00000635155.1:n.471C>A
NM_001282512.1:c.885C>A	NP_001269441.1:p.Thr295=
NM_006440.4:c.885C>A	NP_006431.2:p.Thr295=
NM_001282512.2:c.885C>A	NP_001269441.1:p.Thr295=
NM_001352300.1:c.882C>A	NP_001339229.1:p.Thr294=
NM_001352301.1:c.795C>A	NP_001339230.1:p.Thr265=
NM_001352302.1:c.597C>A	NP_001339231.1:p.Thr199=
NM_001352303.1:c.789C>A	NP_001339232.1:p.Thr263=
NR_147957.1:n.1017C>A
NM_006440.5:c.885C>A MANE Select	NP_006431.2:p.Thr295=
NM_001282512.3:c.885C>A	NP_001269441.1:p.Thr295=
NM_001352300.2:c.882C>A	NP_001339229.1:p.Thr294=
NR_147957.2:n.843C>A
NM_001352301.2:c.795C>A	NP_001339230.1:p.Thr265=
NM_001352302.2:c.597C>A	NP_001339231.1:p.Thr199=
NM_001352303.2:c.789C>A	NP_001339232.1:p.Thr263=