Canonical Allele Identifier: CA2396092160

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895905_19895916delinsGAGAATCCCTCA , CM000684.2:g.19895905_19895916delinsGAGAATCCCTCA	GRCh38
NC_000022.10:g.19883428_19883439delinsGAGAATCCCTCA , CM000684.1:g.19883428_19883439delinsGAGAATCCCTCA	GRCh37
NC_000022.9:g.18263428_18263439delinsGAGAATCCCTCA	NCBI36
NG_011835.1:g.50921_50932delinsTGAGGGATTCTC , LRG_417:g.50921_50932delinsTGAGGGATTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.775-335_775-324delinsTGAGGGATTCTC MANE Select	ENSP00000383365.1:n.775-335_775-324delinsTGAGGGATTCTC
ENST00000334363.14:c.775-335_775-324delinsTGAGGGATTCTC	ENSP00000334451.9:n.775-335_775-324delinsTGAGGGATTCTC
ENST00000400518.5:c.685-335_685-324delinsTGAGGGATTCTC	ENSP00000383362.1:n.685-335_685-324delinsTGAGGGATTCTC
ENST00000400519.6:c.772-335_772-324delinsTGAGGGATTCTC	ENSP00000383363.1:n.772-335_772-324delinsTGAGGGATTCTC
ENST00000400521.6:c.775-335_775-324delinsTGAGGGATTCTC	ENSP00000383365.1:n.775-335_775-324delinsTGAGGGATTCTC
ENST00000400525.6:c.706-335_706-324delinsTGAGGGATTCTC	ENSP00000383369.3:n.706-335_706-324delinsTGAGGGATTCTC
ENST00000474308.5:c.718-335_718-324delinsTGAGGGATTCTC	ENSP00000485665.1:n.718-335_718-324delinsTGAGGGATTCTC
ENST00000475995.3:c.272-335_272-324delinsTGAGGGATTCTC
ENST00000491939.6:c.679-335_679-324delinsTGAGGGATTCTC	ENSP00000485543.1:n.679-335_679-324delinsTGAGGGATTCTC
ENST00000494454.5:n.849-335_849-324delinsTGAGGGATTCTC
ENST00000542719.6:c.487-335_487-324delinsTGAGGGATTCTC	ENSP00000485128.2:n.487-335_487-324delinsTGAGGGATTCTC
ENST00000634537.1:c.4-335_4-324delinsTGAGGGATTCTC	ENSP00000489208.1:n.4-335_4-324delinsTGAGGGATTCTC
ENST00000635155.1:n.361-335_361-324delinsTGAGGGATTCTC
NM_001282512.1:c.775-335_775-324delinsTGAGGGATTCTC	NP_001269441.1:n.775-335_775-324delinsTGAGGGATTCTC
NM_006440.4:c.775-335_775-324delinsTGAGGGATTCTC	NP_006431.2:n.775-335_775-324delinsTGAGGGATTCTC
NM_001282512.2:c.775-335_775-324delinsTGAGGGATTCTC	NP_001269441.1:n.775-335_775-324delinsTGAGGGATTCTC
NM_001352300.1:c.772-335_772-324delinsTGAGGGATTCTC	NP_001339229.1:n.772-335_772-324delinsTGAGGGATTCTC
NM_001352301.1:c.685-335_685-324delinsTGAGGGATTCTC	NP_001339230.1:n.685-335_685-324delinsTGAGGGATTCTC
NM_001352302.1:c.487-335_487-324delinsTGAGGGATTCTC	NP_001339231.1:n.487-335_487-324delinsTGAGGGATTCTC
NM_001352303.1:c.679-335_679-324delinsTGAGGGATTCTC	NP_001339232.1:n.679-335_679-324delinsTGAGGGATTCTC
NR_147957.1:n.907-335_907-324delinsTGAGGGATTCTC
NM_006440.5:c.775-335_775-324delinsTGAGGGATTCTC MANE Select	NP_006431.2:n.775-335_775-324delinsTGAGGGATTCTC
NM_001282512.3:c.775-335_775-324delinsTGAGGGATTCTC	NP_001269441.1:n.775-335_775-324delinsTGAGGGATTCTC
NM_001352300.2:c.772-335_772-324delinsTGAGGGATTCTC	NP_001339229.1:n.772-335_772-324delinsTGAGGGATTCTC
NR_147957.2:n.733-335_733-324delinsTGAGGGATTCTC
NM_001352301.2:c.685-335_685-324delinsTGAGGGATTCTC	NP_001339230.1:n.685-335_685-324delinsTGAGGGATTCTC
NM_001352302.2:c.487-335_487-324delinsTGAGGGATTCTC	NP_001339231.1:n.487-335_487-324delinsTGAGGGATTCTC
NM_001352303.2:c.679-335_679-324delinsTGAGGGATTCTC	NP_001339232.1:n.679-335_679-324delinsTGAGGGATTCTC