Canonical Allele Identifier: CA2396103739

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918897A= , CM000684.2:g.19918897A=	GRCh38
NC_000022.10:g.19906420A= , CM000684.1:g.19906420A=	GRCh37
NC_000022.9:g.18286420A=	NCBI36
NG_011835.1:g.27940T= , LRG_417:g.27940T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.337T= MANE Select	ENSP00000383365.1:p.Tyr113=
ENST00000334363.14:c.337T=	ENSP00000334451.9:p.Tyr113=
ENST00000400518.5:c.247T=	ENSP00000383362.1:p.Tyr83=
ENST00000400519.6:c.334T=	ENSP00000383363.1:p.Tyr112=
ENST00000400521.6:c.337T=	ENSP00000383365.1:p.Tyr113=
ENST00000400525.6:c.268T=	ENSP00000383369.3:p.Tyr90=
ENST00000474308.5:c.280T=	ENSP00000485665.1:p.Tyr94=
ENST00000491939.6:c.241T=	ENSP00000485543.1:p.Tyr81=
ENST00000496729.2:n.342T=
ENST00000542719.6:c.49T=	ENSP00000485128.2:p.Tyr17=
NM_001282512.1:c.337T=	NP_001269441.1:p.Tyr113=
NM_006440.4:c.337T=	NP_006431.2:p.Tyr113=
NM_001282512.2:c.337T=	NP_001269441.1:p.Tyr113=
NM_001352300.1:c.334T=	NP_001339229.1:p.Tyr112=
NM_001352301.1:c.247T=	NP_001339230.1:p.Tyr83=
NM_001352302.1:c.49T=	NP_001339231.1:p.Tyr17=
NM_001352303.1:c.241T=	NP_001339232.1:p.Tyr81=
NR_147957.1:n.469T=
NM_006440.5:c.337T= MANE Select	NP_006431.2:p.Tyr113=
NM_001282512.3:c.337T=	NP_001269441.1:p.Tyr113=
NM_001352300.2:c.334T=	NP_001339229.1:p.Tyr112=
NR_147957.2:n.295T=
NM_001352301.2:c.247T=	NP_001339230.1:p.Tyr83=
NM_001352302.2:c.49T=	NP_001339231.1:p.Tyr17=
NM_001352303.2:c.241T=	NP_001339232.1:p.Tyr81=