Canonical Allele Identifier: CA513365488

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19883072T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895549T>G , CM000684.2:g.19895549T>G	GRCh38
NC_000022.10:g.19883072T>G , CM000684.1:g.19883072T>G	GRCh37
NC_000022.9:g.18263072T>G	NCBI36
NG_011835.1:g.51288A>C , LRG_417:g.51288A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.807A>C MANE Select	ENSP00000383365.1:p.Ala269=
ENST00000334363.14:c.807A>C	ENSP00000334451.9:p.Ala269=
ENST00000400518.5:c.717A>C	ENSP00000383362.1:p.Ala239=
ENST00000400519.6:c.804A>C	ENSP00000383363.1:p.Ala268=
ENST00000400521.6:c.807A>C	ENSP00000383365.1:p.Ala269=
ENST00000400525.6:c.738A>C	ENSP00000383369.3:p.Ala246=
ENST00000474308.5:c.750A>C	ENSP00000485665.1:p.Ala250=
ENST00000475995.3:c.304A>C
ENST00000491939.6:c.711A>C	ENSP00000485543.1:p.Ala237=
ENST00000494454.5:n.881A>C
ENST00000542719.6:c.519A>C	ENSP00000485128.2:p.Ala173=
ENST00000634537.1:c.36A>C	ENSP00000489208.1:p.Ala12=
ENST00000635155.1:n.393A>C
NM_001282512.1:c.807A>C	NP_001269441.1:p.Ala269=
NM_006440.4:c.807A>C	NP_006431.2:p.Ala269=
NM_001282512.2:c.807A>C	NP_001269441.1:p.Ala269=
NM_001352300.1:c.804A>C	NP_001339229.1:p.Ala268=
NM_001352301.1:c.717A>C	NP_001339230.1:p.Ala239=
NM_001352302.1:c.519A>C	NP_001339231.1:p.Ala173=
NM_001352303.1:c.711A>C	NP_001339232.1:p.Ala237=
NR_147957.1:n.939A>C
NM_006440.5:c.807A>C MANE Select	NP_006431.2:p.Ala269=
NM_001282512.3:c.807A>C	NP_001269441.1:p.Ala269=
NM_001352300.2:c.804A>C	NP_001339229.1:p.Ala268=
NR_147957.2:n.765A>C
NM_001352301.2:c.717A>C	NP_001339230.1:p.Ala239=
NM_001352302.2:c.519A>C	NP_001339231.1:p.Ala173=
NM_001352303.2:c.711A>C	NP_001339232.1:p.Ala237=