Canonical Allele Identifier: CA2818396295

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19941136G>A , CM000684.2:g.19941136G>A	GRCh38
NC_000022.10:g.19928659G>A , CM000684.1:g.19928659G>A	GRCh37
NC_000022.9:g.18308659G>A	NCBI36
NG_011526.1:g.4397G>A
NG_011835.1:g.5701C>T , LRG_417:g.5701C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.103+565C>T MANE Select	ENSP00000383365.1:n.103+565C>T
ENST00000334363.14:c.103+565C>T	ENSP00000334451.9:n.103+565C>T
ENST00000400519.6:c.103+565C>T	ENSP00000383363.1:n.103+565C>T
ENST00000400521.6:c.103+565C>T	ENSP00000383365.1:n.103+565C>T
ENST00000400525.6:c.103+565C>T	ENSP00000383369.3:n.103+565C>T
ENST00000474308.5:c.103+565C>T	ENSP00000485665.1:n.103+565C>T
ENST00000496729.2:n.108+565C>T
NM_001282512.1:c.103+565C>T	NP_001269441.1:n.103+565C>T
NM_006440.4:c.103+565C>T	NP_006431.2:n.103+565C>T
NM_001282512.2:c.103+565C>T	NP_001269441.1:n.103+565C>T
NM_001352300.1:c.103+565C>T	NP_001339229.1:n.103+565C>T
NR_147957.1:n.292+565C>T
NM_006440.5:c.103+565C>T MANE Select	NP_006431.2:n.103+565C>T
NM_001282512.3:c.103+565C>T	NP_001269441.1:n.103+565C>T
NM_001352300.2:c.103+565C>T	NP_001339229.1:n.103+565C>T
NR_147957.2:n.118+565C>T