Canonical Allele Identifier: CA2396114897

Gene: TXNRD2

Linked Data

• dbSNP Id: rs1941701107

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19941225_19941226del , CM000684.2:g.19941225_19941226del	GRCh38
NC_000022.10:g.19928748_19928749del , CM000684.1:g.19928748_19928749del	GRCh37
NC_000022.9:g.18308748_18308749del	NCBI36
NG_011526.1:g.4486_4487del
NG_011835.1:g.5611_5612del , LRG_417:g.5611_5612del

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.103+475_103+476del MANE Select	ENSP00000383365.1:n.103+475_103+476del
ENST00000334363.14:c.103+475_103+476del	ENSP00000334451.9:n.103+475_103+476del
ENST00000400519.6:c.103+475_103+476del	ENSP00000383363.1:n.103+475_103+476del
ENST00000400521.6:c.103+475_103+476del	ENSP00000383365.1:n.103+475_103+476del
ENST00000400525.6:c.103+475_103+476del	ENSP00000383369.3:n.103+475_103+476del
ENST00000474308.5:c.103+475_103+476del	ENSP00000485665.1:n.103+475_103+476del
ENST00000496729.2:n.108+475_108+476del
NM_001282512.1:c.103+475_103+476del	NP_001269441.1:n.103+475_103+476del
NM_006440.4:c.103+475_103+476del	NP_006431.2:n.103+475_103+476del
NM_001282512.2:c.103+475_103+476del	NP_001269441.1:n.103+475_103+476del
NM_001352300.1:c.103+475_103+476del	NP_001339229.1:n.103+475_103+476del
NR_147957.1:n.292+475_292+476del
NM_006440.5:c.103+475_103+476del MANE Select	NP_006431.2:n.103+475_103+476del
NM_001282512.3:c.103+475_103+476del	NP_001269441.1:n.103+475_103+476del
NM_001352300.2:c.103+475_103+476del	NP_001339229.1:n.103+475_103+476del
NR_147957.2:n.118+475_118+476del