Canonical Allele Identifier: CA2396103789

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918982G= , CM000684.2:g.19918982G=	GRCh38
NC_000022.10:g.19906505G= , CM000684.1:g.19906505G=	GRCh37
NC_000022.9:g.18286505G=	NCBI36
NG_011835.1:g.27855C= , LRG_417:g.27855C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.252C= MANE Select	ENSP00000383365.1:p.Gly84=
ENST00000334363.14:c.252C=	ENSP00000334451.9:p.Gly84=
ENST00000400518.5:c.162C=	ENSP00000383362.1:p.Gly54=
ENST00000400519.6:c.249C=	ENSP00000383363.1:p.Gly83=
ENST00000400521.6:c.252C=	ENSP00000383365.1:p.Gly84=
ENST00000400525.6:c.183C=	ENSP00000383369.3:p.Gly61=
ENST00000474308.5:c.195C=	ENSP00000485665.1:p.Gly65=
ENST00000491939.6:c.156C=	ENSP00000485543.1:p.Gly52=
ENST00000496729.2:n.257C=
ENST00000542719.6:c.-37C=	ENSP00000485128.2:n.-37C=
NM_001282512.1:c.252C=	NP_001269441.1:p.Gly84=
NM_006440.4:c.252C=	NP_006431.2:p.Gly84=
NM_001282512.2:c.252C=	NP_001269441.1:p.Gly84=
NM_001352300.1:c.249C=	NP_001339229.1:p.Gly83=
NM_001352301.1:c.162C=	NP_001339230.1:p.Gly54=
NM_001352302.1:c.-37C=	NP_001339231.1:n.-37C=
NM_001352303.1:c.156C=	NP_001339232.1:p.Gly52=
NR_147957.1:n.384C=
NM_006440.5:c.252C= MANE Select	NP_006431.2:p.Gly84=
NM_001282512.3:c.252C=	NP_001269441.1:p.Gly84=
NM_001352300.2:c.249C=	NP_001339229.1:p.Gly83=
NR_147957.2:n.210C=
NM_001352301.2:c.162C=	NP_001339230.1:p.Gly54=
NM_001352302.2:c.-37C=	NP_001339231.1:n.-37C=
NM_001352303.2:c.156C=	NP_001339232.1:p.Gly52=