Canonical Allele Identifier: CA2396114647

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19940680G= , CM000684.2:g.19940680G=	GRCh38
NC_000022.10:g.19928203G= , CM000684.1:g.19928203G=	GRCh37
NC_000022.9:g.18308203G=	NCBI36
NG_011526.1:g.3941G=
NG_011835.1:g.6157C= , LRG_417:g.6157C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.103+1021C= MANE Select	ENSP00000383365.1:n.103+1021C=
ENST00000334363.14:c.103+1021C=	ENSP00000334451.9:n.103+1021C=
ENST00000400519.6:c.103+1021C=	ENSP00000383363.1:n.103+1021C=
ENST00000400521.6:c.103+1021C=	ENSP00000383365.1:n.103+1021C=
ENST00000400525.6:c.103+1021C=	ENSP00000383369.3:n.103+1021C=
ENST00000474308.5:c.103+1021C=	ENSP00000485665.1:n.103+1021C=
ENST00000496729.2:n.108+1021C=
NM_001282512.1:c.103+1021C=	NP_001269441.1:n.103+1021C=
NM_006440.4:c.103+1021C=	NP_006431.2:n.103+1021C=
NM_001282512.2:c.103+1021C=	NP_001269441.1:n.103+1021C=
NM_001352300.1:c.103+1021C=	NP_001339229.1:n.103+1021C=
NR_147957.1:n.292+1021C=
NM_006440.5:c.103+1021C= MANE Select	NP_006431.2:n.103+1021C=
NM_001282512.3:c.103+1021C=	NP_001269441.1:n.103+1021C=
NM_001352300.2:c.103+1021C=	NP_001339229.1:n.103+1021C=
NR_147957.2:n.118+1021C=