Canonical Allele Identifier: CA2396091951

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895414C= , CM000684.2:g.19895414C=	GRCh38
NC_000022.10:g.19882937C= , CM000684.1:g.19882937C=	GRCh37
NC_000022.9:g.18262937C=	NCBI36
NG_011835.1:g.51423G= , LRG_417:g.51423G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.942G= MANE Select	ENSP00000383365.1:p.Trp314=
ENST00000334363.14:c.942G=	ENSP00000334451.9:p.Trp314=
ENST00000400518.5:c.852G=	ENSP00000383362.1:p.Trp284=
ENST00000400519.6:c.939G=	ENSP00000383363.1:p.Trp313=
ENST00000400521.6:c.942G=	ENSP00000383365.1:p.Trp314=
ENST00000400525.6:c.873G=	ENSP00000383369.3:p.Trp291=
ENST00000474308.5:c.885G=	ENSP00000485665.1:p.Trp295=
ENST00000475995.3:c.439G=
ENST00000491939.6:c.846G=	ENSP00000485543.1:p.Trp282=
ENST00000494454.5:n.1016G=
ENST00000542719.6:c.654G=	ENSP00000485128.2:p.Trp218=
ENST00000634537.1:c.171G=	ENSP00000489208.1:p.Trp57=
ENST00000635155.1:n.528G=
NM_001282512.1:c.942G=	NP_001269441.1:p.Trp314=
NM_006440.4:c.942G=	NP_006431.2:p.Trp314=
NM_001282512.2:c.942G=	NP_001269441.1:p.Trp314=
NM_001352300.1:c.939G=	NP_001339229.1:p.Trp313=
NM_001352301.1:c.852G=	NP_001339230.1:p.Trp284=
NM_001352302.1:c.654G=	NP_001339231.1:p.Trp218=
NM_001352303.1:c.846G=	NP_001339232.1:p.Trp282=
NR_147957.1:n.1074G=
NM_006440.5:c.942G= MANE Select	NP_006431.2:p.Trp314=
NM_001282512.3:c.942G=	NP_001269441.1:p.Trp314=
NM_001352300.2:c.939G=	NP_001339229.1:p.Trp313=
NR_147957.2:n.900G=
NM_001352301.2:c.852G=	NP_001339230.1:p.Trp284=
NM_001352302.2:c.654G=	NP_001339231.1:p.Trp218=
NM_001352303.2:c.846G=	NP_001339232.1:p.Trp282=