Canonical Allele Identifier: CA410686546

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19882986T>A (hg19) ; chr22:g.19895463T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895463T>A , CM000684.2:g.19895463T>A	GRCh38
NC_000022.10:g.19882986T>A , CM000684.1:g.19882986T>A	GRCh37
NC_000022.9:g.18262986T>A	NCBI36
NG_011835.1:g.51374A>T , LRG_417:g.51374A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.893A>T MANE Select	ENSP00000383365.1:p.Asp298Val
ENST00000334363.14:c.893A>T	ENSP00000334451.9:p.Asp298Val
ENST00000400518.5:c.803A>T	ENSP00000383362.1:p.Asp268Val
ENST00000400519.6:c.890A>T	ENSP00000383363.1:p.Asp297Val
ENST00000400521.6:c.893A>T	ENSP00000383365.1:p.Asp298Val
ENST00000400525.6:c.824A>T	ENSP00000383369.3:p.Asp275Val
ENST00000474308.5:c.836A>T	ENSP00000485665.1:p.Asp279Val
ENST00000475995.3:c.390A>T
ENST00000491939.6:c.797A>T	ENSP00000485543.1:p.Asp266Val
ENST00000494454.5:n.967A>T
ENST00000542719.6:c.605A>T	ENSP00000485128.2:p.Asp202Val
ENST00000634537.1:c.122A>T	ENSP00000489208.1:p.Asp41Val
ENST00000635155.1:n.479A>T
NM_001282512.1:c.893A>T	NP_001269441.1:p.Asp298Val
NM_006440.4:c.893A>T	NP_006431.2:p.Asp298Val
NM_001282512.2:c.893A>T	NP_001269441.1:p.Asp298Val
NM_001352300.1:c.890A>T	NP_001339229.1:p.Asp297Val
NM_001352301.1:c.803A>T	NP_001339230.1:p.Asp268Val
NM_001352302.1:c.605A>T	NP_001339231.1:p.Asp202Val
NM_001352303.1:c.797A>T	NP_001339232.1:p.Asp266Val
NR_147957.1:n.1025A>T
NM_006440.5:c.893A>T MANE Select	NP_006431.2:p.Asp298Val
NM_001282512.3:c.893A>T	NP_001269441.1:p.Asp298Val
NM_001352300.2:c.890A>T	NP_001339229.1:p.Asp297Val
NR_147957.2:n.851A>T
NM_001352301.2:c.803A>T	NP_001339230.1:p.Asp268Val
NM_001352302.2:c.605A>T	NP_001339231.1:p.Asp202Val
NM_001352303.2:c.797A>T	NP_001339232.1:p.Asp266Val