Canonical Allele Identifier: CA410686479

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19882972T>A (hg19) ; chr22:g.19895449T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895449T>A , CM000684.2:g.19895449T>A	GRCh38
NC_000022.10:g.19882972T>A , CM000684.1:g.19882972T>A	GRCh37
NC_000022.9:g.18262972T>A	NCBI36
NG_011835.1:g.51388A>T , LRG_417:g.51388A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.907A>T MANE Select	ENSP00000383365.1:p.Lys303Ter
ENST00000334363.14:c.907A>T	ENSP00000334451.9:p.Lys303Ter
ENST00000400518.5:c.817A>T	ENSP00000383362.1:p.Lys273Ter
ENST00000400519.6:c.904A>T	ENSP00000383363.1:p.Lys302Ter
ENST00000400521.6:c.907A>T	ENSP00000383365.1:p.Lys303Ter
ENST00000400525.6:c.838A>T	ENSP00000383369.3:p.Lys280Ter
ENST00000474308.5:c.850A>T	ENSP00000485665.1:p.Lys284Ter
ENST00000475995.3:c.404A>T
ENST00000491939.6:c.811A>T	ENSP00000485543.1:p.Lys271Ter
ENST00000494454.5:n.981A>T
ENST00000542719.6:c.619A>T	ENSP00000485128.2:p.Lys207Ter
ENST00000634537.1:c.136A>T	ENSP00000489208.1:p.Lys46Ter
ENST00000635155.1:n.493A>T
NM_001282512.1:c.907A>T	NP_001269441.1:p.Lys303Ter
NM_006440.4:c.907A>T	NP_006431.2:p.Lys303Ter
NM_001282512.2:c.907A>T	NP_001269441.1:p.Lys303Ter
NM_001352300.1:c.904A>T	NP_001339229.1:p.Lys302Ter
NM_001352301.1:c.817A>T	NP_001339230.1:p.Lys273Ter
NM_001352302.1:c.619A>T	NP_001339231.1:p.Lys207Ter
NM_001352303.1:c.811A>T	NP_001339232.1:p.Lys271Ter
NR_147957.1:n.1039A>T
NM_006440.5:c.907A>T MANE Select	NP_006431.2:p.Lys303Ter
NM_001282512.3:c.907A>T	NP_001269441.1:p.Lys303Ter
NM_001352300.2:c.904A>T	NP_001339229.1:p.Lys302Ter
NR_147957.2:n.865A>T
NM_001352301.2:c.817A>T	NP_001339230.1:p.Lys273Ter
NM_001352302.2:c.619A>T	NP_001339231.1:p.Lys207Ter
NM_001352303.2:c.811A>T	NP_001339232.1:p.Lys271Ter