Canonical Allele Identifier: CA2396090238
Gene: TXNRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19892037C= , CM000684.2:g.19892037C= GRCh38
NC_000022.10:g.19879560C= , CM000684.1:g.19879560C= GRCh37
NC_000022.9:g.18259560C= NCBI36
NG_011835.1:g.54800G= , LRG_417:g.54800G=

Transcript Alleles

HGVS Amino-acid change
ENST00000400521.7:c.949+3370G= MANE Select ENSP00000383365.1:n.949+3370G=
ENST00000400518.5:c.859+3370G= ENSP00000383362.1:n.859+3370G=
ENST00000400519.6:c.946+3370G= ENSP00000383363.1:n.946+3370G=
ENST00000400521.6:c.949+3370G= ENSP00000383365.1:n.949+3370G=
ENST00000400525.6:c.880+3370G= ENSP00000383369.3:n.880+3370G=
ENST00000474308.5:c.892+3370G= ENSP00000485665.1:n.892+3370G=
ENST00000494454.5:n.1023+3370G=
ENST00000542719.6:c.661+3370G= ENSP00000485128.2:n.661+3370G=
ENST00000634537.1:c.178+3370G= ENSP00000489208.1:n.178+3370G=
ENST00000635155.1:n.536-277G=
NM_006440.4:c.949+3370G= NP_006431.2:n.949+3370G=
NM_001352300.1:c.946+3370G= NP_001339229.1:n.946+3370G=
NM_001352301.1:c.859+3370G= NP_001339230.1:n.859+3370G=
NM_001352302.1:c.661+3370G= NP_001339231.1:n.661+3370G=
NR_147957.1:n.1081+3370G=
NM_006440.5:c.949+3370G= MANE Select NP_006431.2:n.949+3370G=
NM_001352300.2:c.946+3370G= NP_001339229.1:n.946+3370G=
NR_147957.2:n.907+3370G=
NM_001352301.2:c.859+3370G= NP_001339230.1:n.859+3370G=
NM_001352302.2:c.661+3370G= NP_001339231.1:n.661+3370G=