Canonical Allele Identifier: CA2655329464
Gene: TXNRD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19918995del , CM000684.2:g.19918995del GRCh38
NC_000022.10:g.19906518del , CM000684.1:g.19906518del GRCh37
NC_000022.9:g.18286518del NCBI36
NG_011835.1:g.27845del , LRG_417:g.27845del

Transcript Alleles

HGVS Amino-acid Change
ENST00000400521.7:c.242del MANE Select ENSP00000383365.1:p.Gly81AlafsTer16
ENST00000334363.14:c.242del ENSP00000334451.9:p.Gly81AlafsTer16
ENST00000400518.5:c.152del ENSP00000383362.1:p.Gly51AlafsTer16
ENST00000400519.6:c.239del ENSP00000383363.1:p.Gly80AlafsTer16
ENST00000400521.6:c.242del ENSP00000383365.1:p.Gly81AlafsTer16
ENST00000400525.6:c.173del ENSP00000383369.3:p.Gly58AlafsTer16
ENST00000474308.5:c.185del ENSP00000485665.1:p.Gly62AlafsTer16
ENST00000491939.6:c.146del ENSP00000485543.1:p.Gly49AlafsTer16
ENST00000496729.2:n.247del
ENST00000542719.6:c.-47del ENSP00000485128.2:n.-47del
NM_001282512.1:c.242del NP_001269441.1:p.Gly81AlafsTer16
NM_006440.4:c.242del NP_006431.2:p.Gly81AlafsTer16
NM_001282512.2:c.242del NP_001269441.1:p.Gly81AlafsTer16
NM_001352300.1:c.239del NP_001339229.1:p.Gly80AlafsTer16
NM_001352301.1:c.152del NP_001339230.1:p.Gly51AlafsTer16
NM_001352302.1:c.-47del NP_001339231.1:n.-47del
NM_001352303.1:c.146del NP_001339232.1:p.Gly49AlafsTer16
NR_147957.1:n.374del
NM_006440.5:c.242del MANE Select NP_006431.2:p.Gly81AlafsTer16
NM_001282512.3:c.242del NP_001269441.1:p.Gly81AlafsTer16
NM_001352300.2:c.239del NP_001339229.1:p.Gly80AlafsTer16
NR_147957.2:n.200del
NM_001352301.2:c.152del NP_001339230.1:p.Gly51AlafsTer16
NM_001352302.2:c.-47del NP_001339231.1:n.-47del
NM_001352303.2:c.146del NP_001339232.1:p.Gly49AlafsTer16