Canonical Allele Identifier: CA2396092137

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895837_19895841delinsTTAAC , CM000684.2:g.19895837_19895841delinsTTAAC	GRCh38
NC_000022.10:g.19883360_19883364delinsTTAAC , CM000684.1:g.19883360_19883364delinsTTAAC	GRCh37
NC_000022.9:g.18263360_18263364delinsTTAAC	NCBI36
NG_011835.1:g.50996_51000delinsGTTAA , LRG_417:g.50996_51000delinsGTTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.775-260_775-256delinsGTTAA MANE Select	ENSP00000383365.1:n.775-260_775-256delinsGTTAA
ENST00000334363.14:c.775-260_775-256delinsGTTAA	ENSP00000334451.9:n.775-260_775-256delinsGTTAA
ENST00000400518.5:c.685-260_685-256delinsGTTAA	ENSP00000383362.1:n.685-260_685-256delinsGTTAA
ENST00000400519.6:c.772-260_772-256delinsGTTAA	ENSP00000383363.1:n.772-260_772-256delinsGTTAA
ENST00000400521.6:c.775-260_775-256delinsGTTAA	ENSP00000383365.1:n.775-260_775-256delinsGTTAA
ENST00000400525.6:c.706-260_706-256delinsGTTAA	ENSP00000383369.3:n.706-260_706-256delinsGTTAA
ENST00000474308.5:c.718-260_718-256delinsGTTAA	ENSP00000485665.1:n.718-260_718-256delinsGTTAA
ENST00000475995.3:c.272-260_272-256delinsGTTAA
ENST00000491939.6:c.679-260_679-256delinsGTTAA	ENSP00000485543.1:n.679-260_679-256delinsGTTAA
ENST00000494454.5:n.849-260_849-256delinsGTTAA
ENST00000542719.6:c.487-260_487-256delinsGTTAA	ENSP00000485128.2:n.487-260_487-256delinsGTTAA
ENST00000634537.1:c.4-260_4-256delinsGTTAA	ENSP00000489208.1:n.4-260_4-256delinsGTTAA
ENST00000635155.1:n.361-260_361-256delinsGTTAA
NM_001282512.1:c.775-260_775-256delinsGTTAA	NP_001269441.1:n.775-260_775-256delinsGTTAA
NM_006440.4:c.775-260_775-256delinsGTTAA	NP_006431.2:n.775-260_775-256delinsGTTAA
NM_001282512.2:c.775-260_775-256delinsGTTAA	NP_001269441.1:n.775-260_775-256delinsGTTAA
NM_001352300.1:c.772-260_772-256delinsGTTAA	NP_001339229.1:n.772-260_772-256delinsGTTAA
NM_001352301.1:c.685-260_685-256delinsGTTAA	NP_001339230.1:n.685-260_685-256delinsGTTAA
NM_001352302.1:c.487-260_487-256delinsGTTAA	NP_001339231.1:n.487-260_487-256delinsGTTAA
NM_001352303.1:c.679-260_679-256delinsGTTAA	NP_001339232.1:n.679-260_679-256delinsGTTAA
NR_147957.1:n.907-260_907-256delinsGTTAA
NM_006440.5:c.775-260_775-256delinsGTTAA MANE Select	NP_006431.2:n.775-260_775-256delinsGTTAA
NM_001282512.3:c.775-260_775-256delinsGTTAA	NP_001269441.1:n.775-260_775-256delinsGTTAA
NM_001352300.2:c.772-260_772-256delinsGTTAA	NP_001339229.1:n.772-260_772-256delinsGTTAA
NR_147957.2:n.733-260_733-256delinsGTTAA
NM_001352301.2:c.685-260_685-256delinsGTTAA	NP_001339230.1:n.685-260_685-256delinsGTTAA
NM_001352302.2:c.487-260_487-256delinsGTTAA	NP_001339231.1:n.487-260_487-256delinsGTTAA
NM_001352303.2:c.679-260_679-256delinsGTTAA	NP_001339232.1:n.679-260_679-256delinsGTTAA