Canonical Allele Identifier: CA2396091968

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895460C= , CM000684.2:g.19895460C=	GRCh38
NC_000022.10:g.19882983C= , CM000684.1:g.19882983C=	GRCh37
NC_000022.9:g.18262983C=	NCBI36
NG_011835.1:g.51377G= , LRG_417:g.51377G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.896G= MANE Select	ENSP00000383365.1:p.Ser299=
ENST00000334363.14:c.896G=	ENSP00000334451.9:p.Ser299=
ENST00000400518.5:c.806G=	ENSP00000383362.1:p.Ser269=
ENST00000400519.6:c.893G=	ENSP00000383363.1:p.Ser298=
ENST00000400521.6:c.896G=	ENSP00000383365.1:p.Ser299=
ENST00000400525.6:c.827G=	ENSP00000383369.3:p.Ser276=
ENST00000474308.5:c.839G=	ENSP00000485665.1:p.Ser280=
ENST00000475995.3:c.393G=
ENST00000491939.6:c.800G=	ENSP00000485543.1:p.Ser267=
ENST00000494454.5:n.970G=
ENST00000542719.6:c.608G=	ENSP00000485128.2:p.Ser203=
ENST00000634537.1:c.125G=	ENSP00000489208.1:p.Ser42=
ENST00000635155.1:n.482G=
NM_001282512.1:c.896G=	NP_001269441.1:p.Ser299=
NM_006440.4:c.896G=	NP_006431.2:p.Ser299=
NM_001282512.2:c.896G=	NP_001269441.1:p.Ser299=
NM_001352300.1:c.893G=	NP_001339229.1:p.Ser298=
NM_001352301.1:c.806G=	NP_001339230.1:p.Ser269=
NM_001352302.1:c.608G=	NP_001339231.1:p.Ser203=
NM_001352303.1:c.800G=	NP_001339232.1:p.Ser267=
NR_147957.1:n.1028G=
NM_006440.5:c.896G= MANE Select	NP_006431.2:p.Ser299=
NM_001282512.3:c.896G=	NP_001269441.1:p.Ser299=
NM_001352300.2:c.893G=	NP_001339229.1:p.Ser298=
NR_147957.2:n.854G=
NM_001352301.2:c.806G=	NP_001339230.1:p.Ser269=
NM_001352302.2:c.608G=	NP_001339231.1:p.Ser203=
NM_001352303.2:c.800G=	NP_001339232.1:p.Ser267=