Canonical Allele Identifier: CA410694091

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19906519A>T (hg19) ; chr22:g.19918996A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918996A>T , CM000684.2:g.19918996A>T	GRCh38
NC_000022.10:g.19906519A>T , CM000684.1:g.19906519A>T	GRCh37
NC_000022.9:g.18286519A>T	NCBI36
NG_011835.1:g.27841T>A , LRG_417:g.27841T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.238T>A MANE Select	ENSP00000383365.1:p.Trp80Arg
ENST00000334363.14:c.238T>A	ENSP00000334451.9:p.Trp80Arg
ENST00000400518.5:c.148T>A	ENSP00000383362.1:p.Trp50Arg
ENST00000400519.6:c.235T>A	ENSP00000383363.1:p.Trp79Arg
ENST00000400521.6:c.238T>A	ENSP00000383365.1:p.Trp80Arg
ENST00000400525.6:c.169T>A	ENSP00000383369.3:p.Trp57Arg
ENST00000474308.5:c.181T>A	ENSP00000485665.1:p.Trp61Arg
ENST00000491939.6:c.142T>A	ENSP00000485543.1:p.Trp48Arg
ENST00000496729.2:n.243T>A
ENST00000542719.6:c.-51T>A	ENSP00000485128.2:n.-51T>A
NM_001282512.1:c.238T>A	NP_001269441.1:p.Trp80Arg
NM_006440.4:c.238T>A	NP_006431.2:p.Trp80Arg
NM_001282512.2:c.238T>A	NP_001269441.1:p.Trp80Arg
NM_001352300.1:c.235T>A	NP_001339229.1:p.Trp79Arg
NM_001352301.1:c.148T>A	NP_001339230.1:p.Trp50Arg
NM_001352302.1:c.-51T>A	NP_001339231.1:n.-51T>A
NM_001352303.1:c.142T>A	NP_001339232.1:p.Trp48Arg
NR_147957.1:n.370T>A
NM_006440.5:c.238T>A MANE Select	NP_006431.2:p.Trp80Arg
NM_001282512.3:c.238T>A	NP_001269441.1:p.Trp80Arg
NM_001352300.2:c.235T>A	NP_001339229.1:p.Trp79Arg
NR_147957.2:n.196T>A
NM_001352301.2:c.148T>A	NP_001339230.1:p.Trp50Arg
NM_001352302.2:c.-51T>A	NP_001339231.1:n.-51T>A
NM_001352303.2:c.142T>A	NP_001339232.1:p.Trp48Arg