Canonical Allele Identifier: CA2396091966

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895457G= , CM000684.2:g.19895457G=	GRCh38
NC_000022.10:g.19882980G= , CM000684.1:g.19882980G=	GRCh37
NC_000022.9:g.18262980G=	NCBI36
NG_011835.1:g.51380C= , LRG_417:g.51380C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.899C= MANE Select	ENSP00000383365.1:p.Thr300=
ENST00000334363.14:c.899C=	ENSP00000334451.9:p.Thr300=
ENST00000400518.5:c.809C=	ENSP00000383362.1:p.Thr270=
ENST00000400519.6:c.896C=	ENSP00000383363.1:p.Thr299=
ENST00000400521.6:c.899C=	ENSP00000383365.1:p.Thr300=
ENST00000400525.6:c.830C=	ENSP00000383369.3:p.Thr277=
ENST00000474308.5:c.842C=	ENSP00000485665.1:p.Thr281=
ENST00000475995.3:c.396C=
ENST00000491939.6:c.803C=	ENSP00000485543.1:p.Thr268=
ENST00000494454.5:n.973C=
ENST00000542719.6:c.611C=	ENSP00000485128.2:p.Thr204=
ENST00000634537.1:c.128C=	ENSP00000489208.1:p.Thr43=
ENST00000635155.1:n.485C=
NM_001282512.1:c.899C=	NP_001269441.1:p.Thr300=
NM_006440.4:c.899C=	NP_006431.2:p.Thr300=
NM_001282512.2:c.899C=	NP_001269441.1:p.Thr300=
NM_001352300.1:c.896C=	NP_001339229.1:p.Thr299=
NM_001352301.1:c.809C=	NP_001339230.1:p.Thr270=
NM_001352302.1:c.611C=	NP_001339231.1:p.Thr204=
NM_001352303.1:c.803C=	NP_001339232.1:p.Thr268=
NR_147957.1:n.1031C=
NM_006440.5:c.899C= MANE Select	NP_006431.2:p.Thr300=
NM_001282512.3:c.899C=	NP_001269441.1:p.Thr300=
NM_001352300.2:c.896C=	NP_001339229.1:p.Thr299=
NR_147957.2:n.857C=
NM_001352301.2:c.809C=	NP_001339230.1:p.Thr270=
NM_001352302.2:c.611C=	NP_001339231.1:p.Thr204=
NM_001352303.2:c.803C=	NP_001339232.1:p.Thr268=