Canonical Allele Identifier: CA410686716

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19883070G>A (hg19) ; chr22:g.19895547G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895547G>A , CM000684.2:g.19895547G>A	GRCh38
NC_000022.10:g.19883070G>A , CM000684.1:g.19883070G>A	GRCh37
NC_000022.9:g.18263070G>A	NCBI36
NG_011835.1:g.51290C>T , LRG_417:g.51290C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.809C>T MANE Select	ENSP00000383365.1:p.Ser270Phe
ENST00000334363.14:c.809C>T	ENSP00000334451.9:p.Ser270Phe
ENST00000400518.5:c.719C>T	ENSP00000383362.1:p.Ser240Phe
ENST00000400519.6:c.806C>T	ENSP00000383363.1:p.Ser269Phe
ENST00000400521.6:c.809C>T	ENSP00000383365.1:p.Ser270Phe
ENST00000400525.6:c.740C>T	ENSP00000383369.3:p.Ser247Phe
ENST00000474308.5:c.752C>T	ENSP00000485665.1:p.Ser251Phe
ENST00000475995.3:c.306C>T
ENST00000491939.6:c.713C>T	ENSP00000485543.1:p.Ser238Phe
ENST00000494454.5:n.883C>T
ENST00000542719.6:c.521C>T	ENSP00000485128.2:p.Ser174Phe
ENST00000634537.1:c.38C>T	ENSP00000489208.1:p.Ser13Phe
ENST00000635155.1:n.395C>T
NM_001282512.1:c.809C>T	NP_001269441.1:p.Ser270Phe
NM_006440.4:c.809C>T	NP_006431.2:p.Ser270Phe
NM_001282512.2:c.809C>T	NP_001269441.1:p.Ser270Phe
NM_001352300.1:c.806C>T	NP_001339229.1:p.Ser269Phe
NM_001352301.1:c.719C>T	NP_001339230.1:p.Ser240Phe
NM_001352302.1:c.521C>T	NP_001339231.1:p.Ser174Phe
NM_001352303.1:c.713C>T	NP_001339232.1:p.Ser238Phe
NR_147957.1:n.941C>T
NM_006440.5:c.809C>T MANE Select	NP_006431.2:p.Ser270Phe
NM_001282512.3:c.809C>T	NP_001269441.1:p.Ser270Phe
NM_001352300.2:c.806C>T	NP_001339229.1:p.Ser269Phe
NR_147957.2:n.767C>T
NM_001352301.2:c.719C>T	NP_001339230.1:p.Ser240Phe
NM_001352302.2:c.521C>T	NP_001339231.1:p.Ser174Phe
NM_001352303.2:c.713C>T	NP_001339232.1:p.Ser238Phe