Canonical Allele Identifier: CA2842748412

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19940649del , CM000684.2:g.19940649del	GRCh38
NC_000022.10:g.19928172del , CM000684.1:g.19928172del	GRCh37
NC_000022.9:g.18308172del	NCBI36
NG_011526.1:g.3910del
NG_011835.1:g.6192del , LRG_417:g.6192del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.103+1056del MANE Select	ENSP00000383365.1:n.103+1056del
ENST00000334363.14:c.103+1056del	ENSP00000334451.9:n.103+1056del
ENST00000400519.6:c.103+1056del	ENSP00000383363.1:n.103+1056del
ENST00000400521.6:c.103+1056del	ENSP00000383365.1:n.103+1056del
ENST00000400525.6:c.103+1056del	ENSP00000383369.3:n.103+1056del
ENST00000474308.5:c.103+1056del	ENSP00000485665.1:n.103+1056del
ENST00000496729.2:n.108+1056del
NM_001282512.1:c.103+1056del	NP_001269441.1:n.103+1056del
NM_006440.4:c.103+1056del	NP_006431.2:n.103+1056del
NM_001282512.2:c.103+1056del	NP_001269441.1:n.103+1056del
NM_001352300.1:c.103+1056del	NP_001339229.1:n.103+1056del
NR_147957.1:n.292+1056del
NM_006440.5:c.103+1056del MANE Select	NP_006431.2:n.103+1056del
NM_001282512.3:c.103+1056del	NP_001269441.1:n.103+1056del
NM_001352300.2:c.103+1056del	NP_001339229.1:n.103+1056del
NR_147957.2:n.118+1056del