Canonical Allele Identifier: CA16595919

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19931882T>C , CM000684.2:g.19931882T>C	GRCh38
NC_000022.10:g.19919405T>C , CM000684.1:g.19919405T>C	GRCh37
NC_000022.9:g.18299405T>C	NCBI36
NG_011835.1:g.14955A>G , LRG_417:g.14955A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.104-784A>G MANE Select	ENSP00000383365.1:n.104-784A>G
ENST00000334363.14:c.104-784A>G	ENSP00000334451.9:n.104-784A>G
ENST00000400518.5:c.13+475A>G	ENSP00000383362.1:n.13+475A>G
ENST00000400519.6:c.104-787A>G	ENSP00000383363.1:n.104-787A>G
ENST00000400521.6:c.104-784A>G	ENSP00000383365.1:n.104-784A>G
ENST00000400525.6:c.103+9819A>G	ENSP00000383369.3:n.103+9819A>G
ENST00000474308.5:c.104-784A>G	ENSP00000485665.1:n.104-784A>G
ENST00000491939.6:c.8-784A>G	ENSP00000485543.1:n.8-784A>G
ENST00000496729.2:n.109-784A>G
ENST00000542719.6:c.-185-784A>G	ENSP00000485128.2:n.-185-784A>G
NM_001282512.1:c.104-784A>G	NP_001269441.1:n.104-784A>G
NM_006440.4:c.104-784A>G	NP_006431.2:n.104-784A>G
NM_001282512.2:c.104-784A>G	NP_001269441.1:n.104-784A>G
NM_001352300.1:c.104-787A>G	NP_001339229.1:n.104-787A>G
NM_001352301.1:c.13+475A>G	NP_001339230.1:n.13+475A>G
NM_001352302.1:c.-185-784A>G	NP_001339231.1:n.-185-784A>G
NM_001352303.1:c.8-784A>G	NP_001339232.1:n.8-784A>G
NR_147957.1:n.293-784A>G
NM_006440.5:c.104-784A>G MANE Select	NP_006431.2:n.104-784A>G
NM_001282512.3:c.104-784A>G	NP_001269441.1:n.104-784A>G
NM_001352300.2:c.104-787A>G	NP_001339229.1:n.104-787A>G
NR_147957.2:n.119-784A>G
NM_001352301.2:c.13+475A>G	NP_001339230.1:n.13+475A>G
NM_001352302.2:c.-185-784A>G	NP_001339231.1:n.-185-784A>G
NM_001352303.2:c.8-784A>G	NP_001339232.1:n.8-784A>G