Canonical Allele Identifier: CA410693784

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19906432C>A (hg19) ; chr22:g.19918909C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918909C>A , CM000684.2:g.19918909C>A	GRCh38
NC_000022.10:g.19906432C>A , CM000684.1:g.19906432C>A	GRCh37
NC_000022.9:g.18286432C>A	NCBI36
NG_011835.1:g.27928G>T , LRG_417:g.27928G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.325G>T MANE Select	ENSP00000383365.1:p.Asp109Tyr
ENST00000334363.14:c.325G>T	ENSP00000334451.9:p.Asp109Tyr
ENST00000400518.5:c.235G>T	ENSP00000383362.1:p.Asp79Tyr
ENST00000400519.6:c.322G>T	ENSP00000383363.1:p.Asp108Tyr
ENST00000400521.6:c.325G>T	ENSP00000383365.1:p.Asp109Tyr
ENST00000400525.6:c.256G>T	ENSP00000383369.3:p.Asp86Tyr
ENST00000474308.5:c.268G>T	ENSP00000485665.1:p.Asp90Tyr
ENST00000491939.6:c.229G>T	ENSP00000485543.1:p.Asp77Tyr
ENST00000496729.2:n.330G>T
ENST00000542719.6:c.37G>T	ENSP00000485128.2:p.Asp13Tyr
NM_001282512.1:c.325G>T	NP_001269441.1:p.Asp109Tyr
NM_006440.4:c.325G>T	NP_006431.2:p.Asp109Tyr
NM_001282512.2:c.325G>T	NP_001269441.1:p.Asp109Tyr
NM_001352300.1:c.322G>T	NP_001339229.1:p.Asp108Tyr
NM_001352301.1:c.235G>T	NP_001339230.1:p.Asp79Tyr
NM_001352302.1:c.37G>T	NP_001339231.1:p.Asp13Tyr
NM_001352303.1:c.229G>T	NP_001339232.1:p.Asp77Tyr
NR_147957.1:n.457G>T
NM_006440.5:c.325G>T MANE Select	NP_006431.2:p.Asp109Tyr
NM_001282512.3:c.325G>T	NP_001269441.1:p.Asp109Tyr
NM_001352300.2:c.322G>T	NP_001339229.1:p.Asp108Tyr
NR_147957.2:n.283G>T
NM_001352301.2:c.235G>T	NP_001339230.1:p.Asp79Tyr
NM_001352302.2:c.37G>T	NP_001339231.1:p.Asp13Tyr
NM_001352303.2:c.229G>T	NP_001339232.1:p.Asp77Tyr