Canonical Allele Identifier: CA2988033211

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918905dup , CM000684.2:g.19918905dup	GRCh38
NC_000022.10:g.19906428dup , CM000684.1:g.19906428dup	GRCh37
NC_000022.9:g.18286428dup	NCBI36
NG_011835.1:g.27936dup , LRG_417:g.27936dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.333dup MANE Select	ENSP00000383365.1:p.Asn112GlnfsTer13
ENST00000334363.14:c.333dup	ENSP00000334451.9:p.Asn112GlnfsTer13
ENST00000400518.5:c.243dup	ENSP00000383362.1:p.Asn82GlnfsTer13
ENST00000400519.6:c.330dup	ENSP00000383363.1:p.Asn111GlnfsTer13
ENST00000400521.6:c.333dup	ENSP00000383365.1:p.Asn112GlnfsTer13
ENST00000400525.6:c.264dup	ENSP00000383369.3:p.Asn89GlnfsTer13
ENST00000474308.5:c.276dup	ENSP00000485665.1:p.Asn93GlnfsTer13
ENST00000491939.6:c.237dup	ENSP00000485543.1:p.Asn80GlnfsTer13
ENST00000496729.2:n.338dup
ENST00000542719.6:c.45dup	ENSP00000485128.2:p.Asn16GlnfsTer13
NM_001282512.1:c.333dup	NP_001269441.1:p.Asn112GlnfsTer13
NM_006440.4:c.333dup	NP_006431.2:p.Asn112GlnfsTer13
NM_001282512.2:c.333dup	NP_001269441.1:p.Asn112GlnfsTer13
NM_001352300.1:c.330dup	NP_001339229.1:p.Asn111GlnfsTer13
NM_001352301.1:c.243dup	NP_001339230.1:p.Asn82GlnfsTer13
NM_001352302.1:c.45dup	NP_001339231.1:p.Asn16GlnfsTer13
NM_001352303.1:c.237dup	NP_001339232.1:p.Asn80GlnfsTer13
NR_147957.1:n.465dup
NM_006440.5:c.333dup MANE Select	NP_006431.2:p.Asn112GlnfsTer13
NM_001282512.3:c.333dup	NP_001269441.1:p.Asn112GlnfsTer13
NM_001352300.2:c.330dup	NP_001339229.1:p.Asn111GlnfsTer13
NR_147957.2:n.291dup
NM_001352301.2:c.243dup	NP_001339230.1:p.Asn82GlnfsTer13
NM_001352302.2:c.45dup	NP_001339231.1:p.Asn16GlnfsTer13
NM_001352303.2:c.237dup	NP_001339232.1:p.Asn80GlnfsTer13