Canonical Allele Identifier: CA513365139

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19882931T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895408T>G , CM000684.2:g.19895408T>G	GRCh38
NC_000022.10:g.19882931T>G , CM000684.1:g.19882931T>G	GRCh37
NC_000022.9:g.18262931T>G	NCBI36
NG_011835.1:g.51429A>C , LRG_417:g.51429A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.948A>C MANE Select	ENSP00000383365.1:p.Ile316=
ENST00000334363.14:c.948A>C	ENSP00000334451.9:p.Ile316=
ENST00000400518.5:c.858A>C	ENSP00000383362.1:p.Ile286=
ENST00000400519.6:c.945A>C	ENSP00000383363.1:p.Ile315=
ENST00000400521.6:c.948A>C	ENSP00000383365.1:p.Ile316=
ENST00000400525.6:c.879A>C	ENSP00000383369.3:p.Ile293=
ENST00000474308.5:c.891A>C	ENSP00000485665.1:p.Ile297=
ENST00000475995.3:c.445A>C
ENST00000491939.6:c.852A>C	ENSP00000485543.1:p.Ile284=
ENST00000494454.5:n.1022A>C
ENST00000542719.6:c.660A>C	ENSP00000485128.2:p.Ile220=
ENST00000634537.1:c.177A>C	ENSP00000489208.1:p.Ile59=
ENST00000635155.1:n.534A>C
NM_001282512.1:c.948A>C	NP_001269441.1:p.Ile316=
NM_006440.4:c.948A>C	NP_006431.2:p.Ile316=
NM_001282512.2:c.948A>C	NP_001269441.1:p.Ile316=
NM_001352300.1:c.945A>C	NP_001339229.1:p.Ile315=
NM_001352301.1:c.858A>C	NP_001339230.1:p.Ile286=
NM_001352302.1:c.660A>C	NP_001339231.1:p.Ile220=
NM_001352303.1:c.852A>C	NP_001339232.1:p.Ile284=
NR_147957.1:n.1080A>C
NM_006440.5:c.948A>C MANE Select	NP_006431.2:p.Ile316=
NM_001282512.3:c.948A>C	NP_001269441.1:p.Ile316=
NM_001352300.2:c.945A>C	NP_001339229.1:p.Ile315=
NR_147957.2:n.906A>C
NM_001352301.2:c.858A>C	NP_001339230.1:p.Ile286=
NM_001352302.2:c.660A>C	NP_001339231.1:p.Ile220=
NM_001352303.2:c.852A>C	NP_001339232.1:p.Ile284=