Canonical Allele Identifier: CA410693678

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19906402G>T (hg19) ; chr22:g.19918879G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918879G>T , CM000684.2:g.19918879G>T	GRCh38
NC_000022.10:g.19906402G>T , CM000684.1:g.19906402G>T	GRCh37
NC_000022.9:g.18286402G>T	NCBI36
NG_011835.1:g.27958C>A , LRG_417:g.27958C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.355C>A MANE Select	ENSP00000383365.1:p.Gln119Lys
ENST00000334363.14:c.355C>A	ENSP00000334451.9:p.Gln119Lys
ENST00000400518.5:c.265C>A	ENSP00000383362.1:p.Gln89Lys
ENST00000400519.6:c.352C>A	ENSP00000383363.1:p.Gln118Lys
ENST00000400521.6:c.355C>A	ENSP00000383365.1:p.Gln119Lys
ENST00000400525.6:c.286C>A	ENSP00000383369.3:p.Gln96Lys
ENST00000474308.5:c.298C>A	ENSP00000485665.1:p.Gln100Lys
ENST00000491939.6:c.259C>A	ENSP00000485543.1:p.Gln87Lys
ENST00000496729.2:n.360C>A
ENST00000542719.6:c.67C>A	ENSP00000485128.2:p.Gln23Lys
NM_001282512.1:c.355C>A	NP_001269441.1:p.Gln119Lys
NM_006440.4:c.355C>A	NP_006431.2:p.Gln119Lys
NM_001282512.2:c.355C>A	NP_001269441.1:p.Gln119Lys
NM_001352300.1:c.352C>A	NP_001339229.1:p.Gln118Lys
NM_001352301.1:c.265C>A	NP_001339230.1:p.Gln89Lys
NM_001352302.1:c.67C>A	NP_001339231.1:p.Gln23Lys
NM_001352303.1:c.259C>A	NP_001339232.1:p.Gln87Lys
NR_147957.1:n.487C>A
NM_006440.5:c.355C>A MANE Select	NP_006431.2:p.Gln119Lys
NM_001282512.3:c.355C>A	NP_001269441.1:p.Gln119Lys
NM_001352300.2:c.352C>A	NP_001339229.1:p.Gln118Lys
NR_147957.2:n.313C>A
NM_001352301.2:c.265C>A	NP_001339230.1:p.Gln89Lys
NM_001352302.2:c.67C>A	NP_001339231.1:p.Gln23Lys
NM_001352303.2:c.259C>A	NP_001339232.1:p.Gln87Lys