Canonical Allele Identifier: CA2396103740

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918898G= , CM000684.2:g.19918898G=	GRCh38
NC_000022.10:g.19906421G= , CM000684.1:g.19906421G=	GRCh37
NC_000022.9:g.18286421G=	NCBI36
NG_011835.1:g.27939C= , LRG_417:g.27939C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.336C= MANE Select	ENSP00000383365.1:p.Asn112=
ENST00000334363.14:c.336C=	ENSP00000334451.9:p.Asn112=
ENST00000400518.5:c.246C=	ENSP00000383362.1:p.Asn82=
ENST00000400519.6:c.333C=	ENSP00000383363.1:p.Asn111=
ENST00000400521.6:c.336C=	ENSP00000383365.1:p.Asn112=
ENST00000400525.6:c.267C=	ENSP00000383369.3:p.Asn89=
ENST00000474308.5:c.279C=	ENSP00000485665.1:p.Asn93=
ENST00000491939.6:c.240C=	ENSP00000485543.1:p.Asn80=
ENST00000496729.2:n.341C=
ENST00000542719.6:c.48C=	ENSP00000485128.2:p.Asn16=
NM_001282512.1:c.336C=	NP_001269441.1:p.Asn112=
NM_006440.4:c.336C=	NP_006431.2:p.Asn112=
NM_001282512.2:c.336C=	NP_001269441.1:p.Asn112=
NM_001352300.1:c.333C=	NP_001339229.1:p.Asn111=
NM_001352301.1:c.246C=	NP_001339230.1:p.Asn82=
NM_001352302.1:c.48C=	NP_001339231.1:p.Asn16=
NM_001352303.1:c.240C=	NP_001339232.1:p.Asn80=
NR_147957.1:n.468C=
NM_006440.5:c.336C= MANE Select	NP_006431.2:p.Asn112=
NM_001282512.3:c.336C=	NP_001269441.1:p.Asn112=
NM_001352300.2:c.333C=	NP_001339229.1:p.Asn111=
NR_147957.2:n.294C=
NM_001352301.2:c.246C=	NP_001339230.1:p.Asn82=
NM_001352302.2:c.48C=	NP_001339231.1:p.Asn16=
NM_001352303.2:c.240C=	NP_001339232.1:p.Asn80=