Canonical Allele Identifier: CA2396092023

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895592_19895595delinsCAAG , CM000684.2:g.19895592_19895595delinsCAAG	GRCh38
NC_000022.10:g.19883115_19883118delinsCAAG , CM000684.1:g.19883115_19883118delinsCAAG	GRCh37
NC_000022.9:g.18263115_18263118delinsCAAG	NCBI36
NG_011835.1:g.51242_51245delinsCTTG , LRG_417:g.51242_51245delinsCTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.775-14_775-11delinsCTTG MANE Select	ENSP00000383365.1:n.775-14_775-11delinsCTTG
ENST00000334363.14:c.775-14_775-11delinsCTTG	ENSP00000334451.9:n.775-14_775-11delinsCTTG
ENST00000400518.5:c.685-14_685-11delinsCTTG	ENSP00000383362.1:n.685-14_685-11delinsCTTG
ENST00000400519.6:c.772-14_772-11delinsCTTG	ENSP00000383363.1:n.772-14_772-11delinsCTTG
ENST00000400521.6:c.775-14_775-11delinsCTTG	ENSP00000383365.1:n.775-14_775-11delinsCTTG
ENST00000400525.6:c.706-14_706-11delinsCTTG	ENSP00000383369.3:n.706-14_706-11delinsCTTG
ENST00000474308.5:c.718-14_718-11delinsCTTG	ENSP00000485665.1:n.718-14_718-11delinsCTTG
ENST00000475995.3:c.272-14_272-11delinsCTTG
ENST00000491939.6:c.679-14_679-11delinsCTTG	ENSP00000485543.1:n.679-14_679-11delinsCTTG
ENST00000494454.5:n.849-14_849-11delinsCTTG
ENST00000542719.6:c.487-14_487-11delinsCTTG	ENSP00000485128.2:n.487-14_487-11delinsCTTG
ENST00000634537.1:c.4-14_4-11delinsCTTG	ENSP00000489208.1:n.4-14_4-11delinsCTTG
ENST00000635155.1:n.361-14_361-11delinsCTTG
NM_001282512.1:c.775-14_775-11delinsCTTG	NP_001269441.1:n.775-14_775-11delinsCTTG
NM_006440.4:c.775-14_775-11delinsCTTG	NP_006431.2:n.775-14_775-11delinsCTTG
NM_001282512.2:c.775-14_775-11delinsCTTG	NP_001269441.1:n.775-14_775-11delinsCTTG
NM_001352300.1:c.772-14_772-11delinsCTTG	NP_001339229.1:n.772-14_772-11delinsCTTG
NM_001352301.1:c.685-14_685-11delinsCTTG	NP_001339230.1:n.685-14_685-11delinsCTTG
NM_001352302.1:c.487-14_487-11delinsCTTG	NP_001339231.1:n.487-14_487-11delinsCTTG
NM_001352303.1:c.679-14_679-11delinsCTTG	NP_001339232.1:n.679-14_679-11delinsCTTG
NR_147957.1:n.907-14_907-11delinsCTTG
NM_006440.5:c.775-14_775-11delinsCTTG MANE Select	NP_006431.2:n.775-14_775-11delinsCTTG
NM_001282512.3:c.775-14_775-11delinsCTTG	NP_001269441.1:n.775-14_775-11delinsCTTG
NM_001352300.2:c.772-14_772-11delinsCTTG	NP_001339229.1:n.772-14_772-11delinsCTTG
NR_147957.2:n.733-14_733-11delinsCTTG
NM_001352301.2:c.685-14_685-11delinsCTTG	NP_001339230.1:n.685-14_685-11delinsCTTG
NM_001352302.2:c.487-14_487-11delinsCTTG	NP_001339231.1:n.487-14_487-11delinsCTTG
NM_001352303.2:c.679-14_679-11delinsCTTG	NP_001339232.1:n.679-14_679-11delinsCTTG