Canonical Allele Identifier: CA410697020

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19931063C>G , CM000684.2:g.19931063C>G	GRCh38
NC_000022.10:g.19918586C>G , CM000684.1:g.19918586C>G	GRCh37
NC_000022.9:g.18298586C>G	NCBI36
NG_011835.1:g.15774G>C , LRG_417:g.15774G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_006440.5:c.139G>C MANE Select	NP_006431.2:p.Gly47Arg
ENST00000400521.7:c.139G>C MANE Select	ENSP00000383365.1:p.Gly47Arg
NM_001282512.1:c.139G>C	NP_001269441.1:p.Gly47Arg
NM_001282512.2:c.139G>C	NP_001269441.1:p.Gly47Arg
NM_001282512.3:c.139G>C	NP_001269441.1:p.Gly47Arg
NM_001352300.1:c.136G>C	NP_001339229.1:p.Gly46Arg
NM_001352300.2:c.136G>C	NP_001339229.1:p.Gly46Arg
NM_001352301.1:c.49G>C	NP_001339230.1:p.Gly17Arg
NM_001352301.2:c.49G>C	NP_001339230.1:p.Gly17Arg
NM_001352302.1:c.-150G>C	NP_001339231.1:n.-150G>C
NM_001352302.2:c.-150G>C	NP_001339231.1:n.-150G>C
NM_001352303.1:c.43G>C	NP_001339232.1:p.Gly15Arg
NM_001352303.2:c.43G>C	NP_001339232.1:p.Gly15Arg
NM_006440.4:c.139G>C	NP_006431.2:p.Gly47Arg
NR_147957.1:n.328G>C
NR_147957.2:n.154G>C
ENST00000334363.14:c.139G>C	ENSP00000334451.9:p.Gly47Arg
ENST00000400518.5:c.49G>C	ENSP00000383362.1:p.Gly17Arg
ENST00000400519.6:c.136G>C	ENSP00000383363.1:p.Gly46Arg
ENST00000400521.6:c.139G>C	ENSP00000383365.1:p.Gly47Arg
ENST00000400525.6:c.103+10638G>C	ENSP00000383369.3:n.103+10638G>C
ENST00000474308.5:c.139G>C	ENSP00000485665.1:p.Gly47Arg
ENST00000491939.6:c.43G>C	ENSP00000485543.1:p.Gly15Arg
ENST00000496729.2:n.144G>C
ENST00000542719.6:c.-150G>C	ENSP00000485128.2:n.-150G>C