Canonical Allele Identifier: CA2570796332

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19940585T>C , CM000684.2:g.19940585T>C	GRCh38
NC_000022.10:g.19928108T>C , CM000684.1:g.19928108T>C	GRCh37
NC_000022.9:g.18308108T>C	NCBI36
NG_011526.1:g.3846T>C
NG_011835.1:g.6252A>G , LRG_417:g.6252A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.103+1116A>G MANE Select	ENSP00000383365.1:n.103+1116A>G
ENST00000334363.14:c.103+1116A>G	ENSP00000334451.9:n.103+1116A>G
ENST00000400519.6:c.103+1116A>G	ENSP00000383363.1:n.103+1116A>G
ENST00000400521.6:c.103+1116A>G	ENSP00000383365.1:n.103+1116A>G
ENST00000400525.6:c.103+1116A>G	ENSP00000383369.3:n.103+1116A>G
ENST00000474308.5:c.103+1116A>G	ENSP00000485665.1:n.103+1116A>G
ENST00000496729.2:n.108+1116A>G
NM_001282512.1:c.103+1116A>G	NP_001269441.1:n.103+1116A>G
NM_006440.4:c.103+1116A>G	NP_006431.2:n.103+1116A>G
NM_001282512.2:c.103+1116A>G	NP_001269441.1:n.103+1116A>G
NM_001352300.1:c.103+1116A>G	NP_001339229.1:n.103+1116A>G
NR_147957.1:n.292+1116A>G
NM_006440.5:c.103+1116A>G MANE Select	NP_006431.2:n.103+1116A>G
NM_001282512.3:c.103+1116A>G	NP_001269441.1:n.103+1116A>G
NM_001352300.2:c.103+1116A>G	NP_001339229.1:n.103+1116A>G
NR_147957.2:n.118+1116A>G