Canonical Allele Identifier: CA410686662

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19883042A>T (hg19) ; chr22:g.19895519A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895519A>T , CM000684.2:g.19895519A>T	GRCh38
NC_000022.10:g.19883042A>T , CM000684.1:g.19883042A>T	GRCh37
NC_000022.9:g.18263042A>T	NCBI36
NG_011835.1:g.51318T>A , LRG_417:g.51318T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.837T>A MANE Select	ENSP00000383365.1:p.Cys279Ter
ENST00000334363.14:c.837T>A	ENSP00000334451.9:p.Cys279Ter
ENST00000400518.5:c.747T>A	ENSP00000383362.1:p.Cys249Ter
ENST00000400519.6:c.834T>A	ENSP00000383363.1:p.Cys278Ter
ENST00000400521.6:c.837T>A	ENSP00000383365.1:p.Cys279Ter
ENST00000400525.6:c.768T>A	ENSP00000383369.3:p.Cys256Ter
ENST00000474308.5:c.780T>A	ENSP00000485665.1:p.Cys260Ter
ENST00000475995.3:c.334T>A
ENST00000491939.6:c.741T>A	ENSP00000485543.1:p.Cys247Ter
ENST00000494454.5:n.911T>A
ENST00000542719.6:c.549T>A	ENSP00000485128.2:p.Cys183Ter
ENST00000634537.1:c.66T>A	ENSP00000489208.1:p.Cys22Ter
ENST00000635155.1:n.423T>A
NM_001282512.1:c.837T>A	NP_001269441.1:p.Cys279Ter
NM_006440.4:c.837T>A	NP_006431.2:p.Cys279Ter
NM_001282512.2:c.837T>A	NP_001269441.1:p.Cys279Ter
NM_001352300.1:c.834T>A	NP_001339229.1:p.Cys278Ter
NM_001352301.1:c.747T>A	NP_001339230.1:p.Cys249Ter
NM_001352302.1:c.549T>A	NP_001339231.1:p.Cys183Ter
NM_001352303.1:c.741T>A	NP_001339232.1:p.Cys247Ter
NR_147957.1:n.969T>A
NM_006440.5:c.837T>A MANE Select	NP_006431.2:p.Cys279Ter
NM_001282512.3:c.837T>A	NP_001269441.1:p.Cys279Ter
NM_001352300.2:c.834T>A	NP_001339229.1:p.Cys278Ter
NR_147957.2:n.795T>A
NM_001352301.2:c.747T>A	NP_001339230.1:p.Cys249Ter
NM_001352302.2:c.549T>A	NP_001339231.1:p.Cys183Ter
NM_001352303.2:c.741T>A	NP_001339232.1:p.Cys247Ter