Canonical Allele Identifier: CA2580673763

Gene: TXNRD2

Genomic Alleles

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

Transcript Alleles

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