Canonical Allele Identifier: CA2396091970

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895462G= , CM000684.2:g.19895462G=	GRCh38
NC_000022.10:g.19882985G= , CM000684.1:g.19882985G=	GRCh37
NC_000022.9:g.18262985G=	NCBI36
NG_011835.1:g.51375C= , LRG_417:g.51375C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.894C= MANE Select	ENSP00000383365.1:p.Asp298=
ENST00000334363.14:c.894C=	ENSP00000334451.9:p.Asp298=
ENST00000400518.5:c.804C=	ENSP00000383362.1:p.Asp268=
ENST00000400519.6:c.891C=	ENSP00000383363.1:p.Asp297=
ENST00000400521.6:c.894C=	ENSP00000383365.1:p.Asp298=
ENST00000400525.6:c.825C=	ENSP00000383369.3:p.Asp275=
ENST00000474308.5:c.837C=	ENSP00000485665.1:p.Asp279=
ENST00000475995.3:c.391C=
ENST00000491939.6:c.798C=	ENSP00000485543.1:p.Asp266=
ENST00000494454.5:n.968C=
ENST00000542719.6:c.606C=	ENSP00000485128.2:p.Asp202=
ENST00000634537.1:c.123C=	ENSP00000489208.1:p.Asp41=
ENST00000635155.1:n.480C=
NM_001282512.1:c.894C=	NP_001269441.1:p.Asp298=
NM_006440.4:c.894C=	NP_006431.2:p.Asp298=
NM_001282512.2:c.894C=	NP_001269441.1:p.Asp298=
NM_001352300.1:c.891C=	NP_001339229.1:p.Asp297=
NM_001352301.1:c.804C=	NP_001339230.1:p.Asp268=
NM_001352302.1:c.606C=	NP_001339231.1:p.Asp202=
NM_001352303.1:c.798C=	NP_001339232.1:p.Asp266=
NR_147957.1:n.1026C=
NM_006440.5:c.894C= MANE Select	NP_006431.2:p.Asp298=
NM_001282512.3:c.894C=	NP_001269441.1:p.Asp298=
NM_001352300.2:c.891C=	NP_001339229.1:p.Asp297=
NR_147957.2:n.852C=
NM_001352301.2:c.804C=	NP_001339230.1:p.Asp268=
NM_001352302.2:c.606C=	NP_001339231.1:p.Asp202=
NM_001352303.2:c.798C=	NP_001339232.1:p.Asp266=