Canonical Allele Identifier: CA2551070554
Gene: TXNRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19919187_19919188insCGAGTACAGTTATAGAGAGCAGATTCGTG , CM000684.2:g.19919187_19919188insCGAGTACAGTTATAGAGAGCAGATTCGTG GRCh38
NC_000022.10:g.19906710_19906711insCGAGTACAGTTATAGAGAGCAGATTCGTG , CM000684.1:g.19906710_19906711insCGAGTACAGTTATAGAGAGCAGATTCGTG GRCh37
NC_000022.9:g.18286710_18286711insCGAGTACAGTTATAGAGAGCAGATTCGTG NCBI36
NG_011835.1:g.27649_27650insCACGAATCTGCTCTCTATAACTGTACTCG , LRG_417:g.27649_27650insCACGAATCTGCTCTCTATAACTGTACTCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000400521.7:c.230-184_230-183insCACGAATCTGCTCTCTATAACTGTACTCG MANE Select ENSP00000383365.1:n.230-184_230-183insCACGAATCTGCTCTCTATAACTG...
ENST00000334363.14:c.230-184_230-183insCACGAATCTGCTCTCTATAACTGTACTCG ENSP00000334451.9:n.230-184_230-183insCACGAATCTGCTCTCTATAACTG...
ENST00000400518.5:c.140-184_140-183insCACGAATCTGCTCTCTATAACTGTACTCG ENSP00000383362.1:n.140-184_140-183insCACGAATCTGCTCTCTATAACTG...
ENST00000400519.6:c.227-184_227-183insCACGAATCTGCTCTCTATAACTGTACTCG ENSP00000383363.1:n.227-184_227-183insCACGAATCTGCTCTCTATAACTG...
ENST00000400521.6:c.230-184_230-183insCACGAATCTGCTCTCTATAACTGTACTCG ENSP00000383365.1:n.230-184_230-183insCACGAATCTGCTCTCTATAACTG...
ENST00000400525.6:c.161-184_161-183insCACGAATCTGCTCTCTATAACTGTACTCG ENSP00000383369.3:n.161-184_161-183insCACGAATCTGCTCTCTATAACTG...
ENST00000474308.5:c.173-184_173-183insCACGAATCTGCTCTCTATAACTGTACTCG ENSP00000485665.1:n.173-184_173-183insCACGAATCTGCTCTCTATAACTG...
ENST00000491939.6:c.134-184_134-183insCACGAATCTGCTCTCTATAACTGTACTCG ENSP00000485543.1:n.134-184_134-183insCACGAATCTGCTCTCTATAACTG...
ENST00000496729.2:n.235-184_235-183insCACGAATCTGCTCTCTATAACTGTACTCG
ENST00000542719.6:c.-59-184_-59-183insCACGAATCTGCTCTCTATAACTGTACTCG ENSP00000485128.2:n.-59-184_-59-183insCACGAATCTGCTCTCTATAACTG...
NM_001282512.1:c.230-184_230-183insCACGAATCTGCTCTCTATAACTGTACTCG NP_001269441.1:n.230-184_230-183insCACGAATCTGCTCTCTATAACTGTAC...
NM_006440.4:c.230-184_230-183insCACGAATCTGCTCTCTATAACTGTACTCG NP_006431.2:n.230-184_230-183insCACGAATCTGCTCTCTATAACTGTACTCG...
NM_001282512.2:c.230-184_230-183insCACGAATCTGCTCTCTATAACTGTACTCG NP_001269441.1:n.230-184_230-183insCACGAATCTGCTCTCTATAACTGTAC...
NM_001352300.1:c.227-184_227-183insCACGAATCTGCTCTCTATAACTGTACTCG NP_001339229.1:n.227-184_227-183insCACGAATCTGCTCTCTATAACTGTAC...
NM_001352301.1:c.140-184_140-183insCACGAATCTGCTCTCTATAACTGTACTCG NP_001339230.1:n.140-184_140-183insCACGAATCTGCTCTCTATAACTGTAC...
NM_001352302.1:c.-59-184_-59-183insCACGAATCTGCTCTCTATAACTGTACTCG NP_001339231.1:n.-59-184_-59-183insCACGAATCTGCTCTCTATAACTGTAC...
NM_001352303.1:c.134-184_134-183insCACGAATCTGCTCTCTATAACTGTACTCG NP_001339232.1:n.134-184_134-183insCACGAATCTGCTCTCTATAACTGTAC...
NR_147957.1:n.362-184_362-183insCACGAATCTGCTCTCTATAACTGTACTCG
NM_006440.5:c.230-184_230-183insCACGAATCTGCTCTCTATAACTGTACTCG MANE Select NP_006431.2:n.230-184_230-183insCACGAATCTGCTCTCTATAACTGTACTCG...
NM_001282512.3:c.230-184_230-183insCACGAATCTGCTCTCTATAACTGTACTCG NP_001269441.1:n.230-184_230-183insCACGAATCTGCTCTCTATAACTGTAC...
NM_001352300.2:c.227-184_227-183insCACGAATCTGCTCTCTATAACTGTACTCG NP_001339229.1:n.227-184_227-183insCACGAATCTGCTCTCTATAACTGTAC...
NR_147957.2:n.188-184_188-183insCACGAATCTGCTCTCTATAACTGTACTCG
NM_001352301.2:c.140-184_140-183insCACGAATCTGCTCTCTATAACTGTACTCG NP_001339230.1:n.140-184_140-183insCACGAATCTGCTCTCTATAACTGTAC...
NM_001352302.2:c.-59-184_-59-183insCACGAATCTGCTCTCTATAACTGTACTCG NP_001339231.1:n.-59-184_-59-183insCACGAATCTGCTCTCTATAACTGTAC...
NM_001352303.2:c.134-184_134-183insCACGAATCTGCTCTCTATAACTGTACTCG NP_001339232.1:n.134-184_134-183insCACGAATCTGCTCTCTATAACTGTAC...