Canonical Allele Identifier: CA410693754

Gene: TXNRD2

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918900T>G , CM000684.2:g.19918900T>G	GRCh38
NC_000022.10:g.19906423T>G , CM000684.1:g.19906423T>G	GRCh37
NC_000022.9:g.18286423T>G	NCBI36
NG_011835.1:g.27937A>C , LRG_417:g.27937A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.334A>C MANE Select	ENSP00000383365.1:p.Asn112His
ENST00000334363.14:c.334A>C	ENSP00000334451.9:p.Asn112His
ENST00000400518.5:c.244A>C	ENSP00000383362.1:p.Asn82His
ENST00000400519.6:c.331A>C	ENSP00000383363.1:p.Asn111His
ENST00000400521.6:c.334A>C	ENSP00000383365.1:p.Asn112His
ENST00000400525.6:c.265A>C	ENSP00000383369.3:p.Asn89His
ENST00000474308.5:c.277A>C	ENSP00000485665.1:p.Asn93His
ENST00000491939.6:c.238A>C	ENSP00000485543.1:p.Asn80His
ENST00000496729.2:n.339A>C
ENST00000542719.6:c.46A>C	ENSP00000485128.2:p.Asn16His
NM_001282512.1:c.334A>C	NP_001269441.1:p.Asn112His
NM_006440.4:c.334A>C	NP_006431.2:p.Asn112His
NM_001282512.2:c.334A>C	NP_001269441.1:p.Asn112His
NM_001352300.1:c.331A>C	NP_001339229.1:p.Asn111His
NM_001352301.1:c.244A>C	NP_001339230.1:p.Asn82His
NM_001352302.1:c.46A>C	NP_001339231.1:p.Asn16His
NM_001352303.1:c.238A>C	NP_001339232.1:p.Asn80His
NR_147957.1:n.466A>C
NM_006440.5:c.334A>C MANE Select	NP_006431.2:p.Asn112His
NM_001282512.3:c.334A>C	NP_001269441.1:p.Asn112His
NM_001352300.2:c.331A>C	NP_001339229.1:p.Asn111His
NR_147957.2:n.292A>C
NM_001352301.2:c.244A>C	NP_001339230.1:p.Asn82His
NM_001352302.2:c.46A>C	NP_001339231.1:p.Asn16His
NM_001352303.2:c.238A>C	NP_001339232.1:p.Asn80His