Canonical Allele Identifier: CA1024148020

Gene: TXNRD2

Linked Data

• gnomAD v3: 22-19919275-A-ACCCTCC
• gnomAD v4: 22-19919275-A-ACCCTCC

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19919275_19919276insCCCTCC , CM000684.2:g.19919275_19919276insCCCTCC	GRCh38
NC_000022.10:g.19906798_19906799insCCCTCC , CM000684.1:g.19906798_19906799insCCCTCC	GRCh37
NC_000022.9:g.18286798_18286799insCCCTCC	NCBI36
NG_011835.1:g.27561_27562insGGAGGG , LRG_417:g.27561_27562insGGAGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.229+267_229+268insGGAGGG MANE Select	ENSP00000383365.1:n.229+267_229+268insGGAGGG
ENST00000334363.14:c.229+267_229+268insGGAGGG	ENSP00000334451.9:n.229+267_229+268insGGAGGG
ENST00000400518.5:c.139+267_139+268insGGAGGG	ENSP00000383362.1:n.139+267_139+268insGGAGGG
ENST00000400519.6:c.226+267_226+268insGGAGGG	ENSP00000383363.1:n.226+267_226+268insGGAGGG
ENST00000400521.6:c.229+267_229+268insGGAGGG	ENSP00000383365.1:n.229+267_229+268insGGAGGG
ENST00000400525.6:c.160+267_160+268insGGAGGG	ENSP00000383369.3:n.160+267_160+268insGGAGGG
ENST00000474308.5:c.173-272_173-271insGGAGGG	ENSP00000485665.1:n.173-272_173-271insGGAGGG
ENST00000491939.6:c.133+267_133+268insGGAGGG	ENSP00000485543.1:n.133+267_133+268insGGAGGG
ENST00000496729.2:n.234+267_234+268insGGAGGG
ENST00000542719.6:c.-60+267_-60+268insGGAGGG	ENSP00000485128.2:n.-60+267_-60+268insGGAGGG
NM_001282512.1:c.229+267_229+268insGGAGGG	NP_001269441.1:n.229+267_229+268insGGAGGG
NM_006440.4:c.229+267_229+268insGGAGGG	NP_006431.2:n.229+267_229+268insGGAGGG
NM_001282512.2:c.229+267_229+268insGGAGGG	NP_001269441.1:n.229+267_229+268insGGAGGG
NM_001352300.1:c.226+267_226+268insGGAGGG	NP_001339229.1:n.226+267_226+268insGGAGGG
NM_001352301.1:c.139+267_139+268insGGAGGG	NP_001339230.1:n.139+267_139+268insGGAGGG
NM_001352302.1:c.-60+267_-60+268insGGAGGG	NP_001339231.1:n.-60+267_-60+268insGGAGGG
NM_001352303.1:c.133+267_133+268insGGAGGG	NP_001339232.1:n.133+267_133+268insGGAGGG
NR_147957.1:n.362-272_362-271insGGAGGG
NM_006440.5:c.229+267_229+268insGGAGGG MANE Select	NP_006431.2:n.229+267_229+268insGGAGGG
NM_001282512.3:c.229+267_229+268insGGAGGG	NP_001269441.1:n.229+267_229+268insGGAGGG
NM_001352300.2:c.226+267_226+268insGGAGGG	NP_001339229.1:n.226+267_226+268insGGAGGG
NR_147957.2:n.188-272_188-271insGGAGGG
NM_001352301.2:c.139+267_139+268insGGAGGG	NP_001339230.1:n.139+267_139+268insGGAGGG
NM_001352302.2:c.-60+267_-60+268insGGAGGG	NP_001339231.1:n.-60+267_-60+268insGGAGGG
NM_001352303.2:c.133+267_133+268insGGAGGG	NP_001339232.1:n.133+267_133+268insGGAGGG