Canonical Allele Identifier: CA410686435

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19882965T>A (hg19) ; chr22:g.19895442T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895442T>A , CM000684.2:g.19895442T>A	GRCh38
NC_000022.10:g.19882965T>A , CM000684.1:g.19882965T>A	GRCh37
NC_000022.9:g.18262965T>A	NCBI36
NG_011835.1:g.51395A>T , LRG_417:g.51395A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.914A>T MANE Select	ENSP00000383365.1:p.Asp305Val
ENST00000334363.14:c.914A>T	ENSP00000334451.9:p.Asp305Val
ENST00000400518.5:c.824A>T	ENSP00000383362.1:p.Asp275Val
ENST00000400519.6:c.911A>T	ENSP00000383363.1:p.Asp304Val
ENST00000400521.6:c.914A>T	ENSP00000383365.1:p.Asp305Val
ENST00000400525.6:c.845A>T	ENSP00000383369.3:p.Asp282Val
ENST00000474308.5:c.857A>T	ENSP00000485665.1:p.Asp286Val
ENST00000475995.3:c.411A>T
ENST00000491939.6:c.818A>T	ENSP00000485543.1:p.Asp273Val
ENST00000494454.5:n.988A>T
ENST00000542719.6:c.626A>T	ENSP00000485128.2:p.Asp209Val
ENST00000634537.1:c.143A>T	ENSP00000489208.1:p.Asp48Val
ENST00000635155.1:n.500A>T
NM_001282512.1:c.914A>T	NP_001269441.1:p.Asp305Val
NM_006440.4:c.914A>T	NP_006431.2:p.Asp305Val
NM_001282512.2:c.914A>T	NP_001269441.1:p.Asp305Val
NM_001352300.1:c.911A>T	NP_001339229.1:p.Asp304Val
NM_001352301.1:c.824A>T	NP_001339230.1:p.Asp275Val
NM_001352302.1:c.626A>T	NP_001339231.1:p.Asp209Val
NM_001352303.1:c.818A>T	NP_001339232.1:p.Asp273Val
NR_147957.1:n.1046A>T
NM_006440.5:c.914A>T MANE Select	NP_006431.2:p.Asp305Val
NM_001282512.3:c.914A>T	NP_001269441.1:p.Asp305Val
NM_001352300.2:c.911A>T	NP_001339229.1:p.Asp304Val
NR_147957.2:n.872A>T
NM_001352301.2:c.824A>T	NP_001339230.1:p.Asp275Val
NM_001352302.2:c.626A>T	NP_001339231.1:p.Asp209Val
NM_001352303.2:c.818A>T	NP_001339232.1:p.Asp273Val