Canonical Allele Identifier: CA2396103904
Gene: TXNRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19919197_19919202delinsATTAAT , CM000684.2:g.19919197_19919202delinsATTAAT GRCh38
NC_000022.10:g.19906720_19906725delinsATTAAT , CM000684.1:g.19906720_19906725delinsATTAAT GRCh37
NC_000022.9:g.18286720_18286725delinsATTAAT NCBI36
NG_011835.1:g.27635_27640delinsATTAAT , LRG_417:g.27635_27640delinsATTAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000400521.7:c.230-198_230-193delinsATTAAT MANE Select ENSP00000383365.1:n.230-198_230-193delinsATTAAT
ENST00000334363.14:c.230-198_230-193delinsATTAAT ENSP00000334451.9:n.230-198_230-193delinsATTAAT
ENST00000400518.5:c.140-198_140-193delinsATTAAT ENSP00000383362.1:n.140-198_140-193delinsATTAAT
ENST00000400519.6:c.227-198_227-193delinsATTAAT ENSP00000383363.1:n.227-198_227-193delinsATTAAT
ENST00000400521.6:c.230-198_230-193delinsATTAAT ENSP00000383365.1:n.230-198_230-193delinsATTAAT
ENST00000400525.6:c.161-198_161-193delinsATTAAT ENSP00000383369.3:n.161-198_161-193delinsATTAAT
ENST00000474308.5:c.173-198_173-193delinsATTAAT ENSP00000485665.1:n.173-198_173-193delinsATTAAT
ENST00000491939.6:c.134-198_134-193delinsATTAAT ENSP00000485543.1:n.134-198_134-193delinsATTAAT
ENST00000496729.2:n.235-198_235-193delinsATTAAT
ENST00000542719.6:c.-59-198_-59-193delinsATTAAT ENSP00000485128.2:n.-59-198_-59-193delinsATTAAT
NM_001282512.1:c.230-198_230-193delinsATTAAT NP_001269441.1:n.230-198_230-193delinsATTAAT
NM_006440.4:c.230-198_230-193delinsATTAAT NP_006431.2:n.230-198_230-193delinsATTAAT
NM_001282512.2:c.230-198_230-193delinsATTAAT NP_001269441.1:n.230-198_230-193delinsATTAAT
NM_001352300.1:c.227-198_227-193delinsATTAAT NP_001339229.1:n.227-198_227-193delinsATTAAT
NM_001352301.1:c.140-198_140-193delinsATTAAT NP_001339230.1:n.140-198_140-193delinsATTAAT
NM_001352302.1:c.-59-198_-59-193delinsATTAAT NP_001339231.1:n.-59-198_-59-193delinsATTAAT
NM_001352303.1:c.134-198_134-193delinsATTAAT NP_001339232.1:n.134-198_134-193delinsATTAAT
NR_147957.1:n.362-198_362-193delinsATTAAT
NM_006440.5:c.230-198_230-193delinsATTAAT MANE Select NP_006431.2:n.230-198_230-193delinsATTAAT
NM_001282512.3:c.230-198_230-193delinsATTAAT NP_001269441.1:n.230-198_230-193delinsATTAAT
NM_001352300.2:c.227-198_227-193delinsATTAAT NP_001339229.1:n.227-198_227-193delinsATTAAT
NR_147957.2:n.188-198_188-193delinsATTAAT
NM_001352301.2:c.140-198_140-193delinsATTAAT NP_001339230.1:n.140-198_140-193delinsATTAAT
NM_001352302.2:c.-59-198_-59-193delinsATTAAT NP_001339231.1:n.-59-198_-59-193delinsATTAAT
NM_001352303.2:c.134-198_134-193delinsATTAAT NP_001339232.1:n.134-198_134-193delinsATTAAT