Canonical Allele Identifier: CA751471405

Gene: TXNRD2

Linked Data

• dbSNP Id: rs1315279221
• gnomAD v3: 22-19940671-CCTTTT-C
• gnomAD v4: 22-19940671-CCTTTT-C
• MyVariant Identifiers: chr22:g.19928195_19928199del (hg19) ; chr22:g.19940672_19940676del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19940672_19940676del , CM000684.2:g.19940672_19940676del	GRCh38
NC_000022.10:g.19928195_19928199del , CM000684.1:g.19928195_19928199del	GRCh37
NC_000022.9:g.18308195_18308199del	NCBI36
NG_011526.1:g.3933_3937del
NG_011835.1:g.6161_6165del , LRG_417:g.6161_6165del

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.103+1025_103+1029del MANE Select	ENSP00000383365.1:n.103+1025_103+1029del
ENST00000334363.14:c.103+1025_103+1029del	ENSP00000334451.9:n.103+1025_103+1029del
ENST00000400519.6:c.103+1025_103+1029del	ENSP00000383363.1:n.103+1025_103+1029del
ENST00000400521.6:c.103+1025_103+1029del	ENSP00000383365.1:n.103+1025_103+1029del
ENST00000400525.6:c.103+1025_103+1029del	ENSP00000383369.3:n.103+1025_103+1029del
ENST00000474308.5:c.103+1025_103+1029del	ENSP00000485665.1:n.103+1025_103+1029del
ENST00000496729.2:n.108+1025_108+1029del
NM_001282512.1:c.103+1025_103+1029del	NP_001269441.1:n.103+1025_103+1029del
NM_006440.4:c.103+1025_103+1029del	NP_006431.2:n.103+1025_103+1029del
NM_001282512.2:c.103+1025_103+1029del	NP_001269441.1:n.103+1025_103+1029del
NM_001352300.1:c.103+1025_103+1029del	NP_001339229.1:n.103+1025_103+1029del
NR_147957.1:n.292+1025_292+1029del
NM_006440.5:c.103+1025_103+1029del MANE Select	NP_006431.2:n.103+1025_103+1029del
NM_001282512.3:c.103+1025_103+1029del	NP_001269441.1:n.103+1025_103+1029del
NM_001352300.2:c.103+1025_103+1029del	NP_001339229.1:n.103+1025_103+1029del
NR_147957.2:n.118+1025_118+1029del