Canonical Allele Identifier: CA10104310

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19919595G>A , CM000684.2:g.19919595G>A	GRCh38
NC_000022.10:g.19907118G>A , CM000684.1:g.19907118G>A	GRCh37
NC_000022.9:g.18287118G>A	NCBI36
NG_011835.1:g.27242C>T , LRG_417:g.27242C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006440.5:c.177C>T MANE Select	NP_006431.2:p.Ala59=
ENST00000400521.7:c.177C>T MANE Select	ENSP00000383365.1:p.Ala59=
NM_001282512.1:c.177C>T	NP_001269441.1:p.Ala59=
NM_001282512.2:c.177C>T	NP_001269441.1:p.Ala59=
NM_001282512.3:c.177C>T	NP_001269441.1:p.Ala59=
NM_001352300.1:c.174C>T	NP_001339229.1:p.Ala58=
NM_001352300.2:c.174C>T	NP_001339229.1:p.Ala58=
NM_001352301.1:c.87C>T	NP_001339230.1:p.Ala29=
NM_001352301.2:c.87C>T	NP_001339230.1:p.Ala29=
NM_001352302.1:c.-112C>T	NP_001339231.1:n.-112C>T
NM_001352302.2:c.-112C>T	NP_001339231.1:n.-112C>T
NM_001352303.1:c.81C>T	NP_001339232.1:p.Ala27=
NM_001352303.2:c.81C>T	NP_001339232.1:p.Ala27=
NM_006440.4:c.177C>T	NP_006431.2:p.Ala59=
NR_147957.1:n.362-591C>T
NR_147957.2:n.188-591C>T
ENST00000334363.14:c.177C>T	ENSP00000334451.9:p.Ala59=
ENST00000400518.5:c.87C>T	ENSP00000383362.1:p.Ala29=
ENST00000400519.6:c.174C>T	ENSP00000383363.1:p.Ala58=
ENST00000400521.6:c.177C>T	ENSP00000383365.1:p.Ala59=
ENST00000400525.6:c.108C>T	ENSP00000383369.3:p.Ala36=
ENST00000474308.5:c.173-591C>T	ENSP00000485665.1:n.173-591C>T
ENST00000491939.6:c.81C>T	ENSP00000485543.1:p.Ala27=
ENST00000496729.2:n.182C>T
ENST00000542719.6:c.-112C>T	ENSP00000485128.2:n.-112C>T