Canonical Allele Identifier: CA2396092062
Gene: TXNRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19895677_19895680delinsAGAG , CM000684.2:g.19895677_19895680delinsAGAG GRCh38
NC_000022.10:g.19883200_19883203delinsAGAG , CM000684.1:g.19883200_19883203delinsAGAG GRCh37
NC_000022.9:g.18263200_18263203delinsAGAG NCBI36
NG_011835.1:g.51157_51160delinsCTCT , LRG_417:g.51157_51160delinsCTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000400521.7:c.775-99_775-96delinsCTCT MANE Select ENSP00000383365.1:n.775-99_775-96delinsCTCT
ENST00000334363.14:c.775-99_775-96delinsCTCT ENSP00000334451.9:n.775-99_775-96delinsCTCT
ENST00000400518.5:c.685-99_685-96delinsCTCT ENSP00000383362.1:n.685-99_685-96delinsCTCT
ENST00000400519.6:c.772-99_772-96delinsCTCT ENSP00000383363.1:n.772-99_772-96delinsCTCT
ENST00000400521.6:c.775-99_775-96delinsCTCT ENSP00000383365.1:n.775-99_775-96delinsCTCT
ENST00000400525.6:c.706-99_706-96delinsCTCT ENSP00000383369.3:n.706-99_706-96delinsCTCT
ENST00000474308.5:c.718-99_718-96delinsCTCT ENSP00000485665.1:n.718-99_718-96delinsCTCT
ENST00000475995.3:c.272-99_272-96delinsCTCT
ENST00000491939.6:c.679-99_679-96delinsCTCT ENSP00000485543.1:n.679-99_679-96delinsCTCT
ENST00000494454.5:n.849-99_849-96delinsCTCT
ENST00000542719.6:c.487-99_487-96delinsCTCT ENSP00000485128.2:n.487-99_487-96delinsCTCT
ENST00000634537.1:c.4-99_4-96delinsCTCT ENSP00000489208.1:n.4-99_4-96delinsCTCT
ENST00000635155.1:n.361-99_361-96delinsCTCT
NM_001282512.1:c.775-99_775-96delinsCTCT NP_001269441.1:n.775-99_775-96delinsCTCT
NM_006440.4:c.775-99_775-96delinsCTCT NP_006431.2:n.775-99_775-96delinsCTCT
NM_001282512.2:c.775-99_775-96delinsCTCT NP_001269441.1:n.775-99_775-96delinsCTCT
NM_001352300.1:c.772-99_772-96delinsCTCT NP_001339229.1:n.772-99_772-96delinsCTCT
NM_001352301.1:c.685-99_685-96delinsCTCT NP_001339230.1:n.685-99_685-96delinsCTCT
NM_001352302.1:c.487-99_487-96delinsCTCT NP_001339231.1:n.487-99_487-96delinsCTCT
NM_001352303.1:c.679-99_679-96delinsCTCT NP_001339232.1:n.679-99_679-96delinsCTCT
NR_147957.1:n.907-99_907-96delinsCTCT
NM_006440.5:c.775-99_775-96delinsCTCT MANE Select NP_006431.2:n.775-99_775-96delinsCTCT
NM_001282512.3:c.775-99_775-96delinsCTCT NP_001269441.1:n.775-99_775-96delinsCTCT
NM_001352300.2:c.772-99_772-96delinsCTCT NP_001339229.1:n.772-99_772-96delinsCTCT
NR_147957.2:n.733-99_733-96delinsCTCT
NM_001352301.2:c.685-99_685-96delinsCTCT NP_001339230.1:n.685-99_685-96delinsCTCT
NM_001352302.2:c.487-99_487-96delinsCTCT NP_001339231.1:n.487-99_487-96delinsCTCT
NM_001352303.2:c.679-99_679-96delinsCTCT NP_001339232.1:n.679-99_679-96delinsCTCT