Canonical Allele Identifier: CA2396103798

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918994C= , CM000684.2:g.19918994C=	GRCh38
NC_000022.10:g.19906517C= , CM000684.1:g.19906517C=	GRCh37
NC_000022.9:g.18286517C=	NCBI36
NG_011835.1:g.27843G= , LRG_417:g.27843G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.240G= MANE Select	ENSP00000383365.1:p.Trp80=
ENST00000334363.14:c.240G=	ENSP00000334451.9:p.Trp80=
ENST00000400518.5:c.150G=	ENSP00000383362.1:p.Trp50=
ENST00000400519.6:c.237G=	ENSP00000383363.1:p.Trp79=
ENST00000400521.6:c.240G=	ENSP00000383365.1:p.Trp80=
ENST00000400525.6:c.171G=	ENSP00000383369.3:p.Trp57=
ENST00000474308.5:c.183G=	ENSP00000485665.1:p.Trp61=
ENST00000491939.6:c.144G=	ENSP00000485543.1:p.Trp48=
ENST00000496729.2:n.245G=
ENST00000542719.6:c.-49G=	ENSP00000485128.2:n.-49G=
NM_001282512.1:c.240G=	NP_001269441.1:p.Trp80=
NM_006440.4:c.240G=	NP_006431.2:p.Trp80=
NM_001282512.2:c.240G=	NP_001269441.1:p.Trp80=
NM_001352300.1:c.237G=	NP_001339229.1:p.Trp79=
NM_001352301.1:c.150G=	NP_001339230.1:p.Trp50=
NM_001352302.1:c.-49G=	NP_001339231.1:n.-49G=
NM_001352303.1:c.144G=	NP_001339232.1:p.Trp48=
NR_147957.1:n.372G=
NM_006440.5:c.240G= MANE Select	NP_006431.2:p.Trp80=
NM_001282512.3:c.240G=	NP_001269441.1:p.Trp80=
NM_001352300.2:c.237G=	NP_001339229.1:p.Trp79=
NR_147957.2:n.198G=
NM_001352301.2:c.150G=	NP_001339230.1:p.Trp50=
NM_001352302.2:c.-49G=	NP_001339231.1:n.-49G=
NM_001352303.2:c.144G=	NP_001339232.1:p.Trp48=