Canonical Allele Identifier: CA410686719

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19883071A>C (hg19) ; chr22:g.19895548A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895548A>C , CM000684.2:g.19895548A>C	GRCh38
NC_000022.10:g.19883071A>C , CM000684.1:g.19883071A>C	GRCh37
NC_000022.9:g.18263071A>C	NCBI36
NG_011835.1:g.51289T>G , LRG_417:g.51289T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.808T>G MANE Select	ENSP00000383365.1:p.Ser270Ala
ENST00000334363.14:c.808T>G	ENSP00000334451.9:p.Ser270Ala
ENST00000400518.5:c.718T>G	ENSP00000383362.1:p.Ser240Ala
ENST00000400519.6:c.805T>G	ENSP00000383363.1:p.Ser269Ala
ENST00000400521.6:c.808T>G	ENSP00000383365.1:p.Ser270Ala
ENST00000400525.6:c.739T>G	ENSP00000383369.3:p.Ser247Ala
ENST00000474308.5:c.751T>G	ENSP00000485665.1:p.Ser251Ala
ENST00000475995.3:c.305T>G
ENST00000491939.6:c.712T>G	ENSP00000485543.1:p.Ser238Ala
ENST00000494454.5:n.882T>G
ENST00000542719.6:c.520T>G	ENSP00000485128.2:p.Ser174Ala
ENST00000634537.1:c.37T>G	ENSP00000489208.1:p.Ser13Ala
ENST00000635155.1:n.394T>G
NM_001282512.1:c.808T>G	NP_001269441.1:p.Ser270Ala
NM_006440.4:c.808T>G	NP_006431.2:p.Ser270Ala
NM_001282512.2:c.808T>G	NP_001269441.1:p.Ser270Ala
NM_001352300.1:c.805T>G	NP_001339229.1:p.Ser269Ala
NM_001352301.1:c.718T>G	NP_001339230.1:p.Ser240Ala
NM_001352302.1:c.520T>G	NP_001339231.1:p.Ser174Ala
NM_001352303.1:c.712T>G	NP_001339232.1:p.Ser238Ala
NR_147957.1:n.940T>G
NM_006440.5:c.808T>G MANE Select	NP_006431.2:p.Ser270Ala
NM_001282512.3:c.808T>G	NP_001269441.1:p.Ser270Ala
NM_001352300.2:c.805T>G	NP_001339229.1:p.Ser269Ala
NR_147957.2:n.766T>G
NM_001352301.2:c.718T>G	NP_001339230.1:p.Ser240Ala
NM_001352302.2:c.520T>G	NP_001339231.1:p.Ser174Ala
NM_001352303.2:c.712T>G	NP_001339232.1:p.Ser238Ala