Canonical Allele Identifier: CA410693789

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19906433T>A (hg19) ; chr22:g.19918910T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918910T>A , CM000684.2:g.19918910T>A	GRCh38
NC_000022.10:g.19906433T>A , CM000684.1:g.19906433T>A	GRCh37
NC_000022.9:g.18286433T>A	NCBI36
NG_011835.1:g.27927A>T , LRG_417:g.27927A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.324A>T MANE Select	ENSP00000383365.1:p.Gln108His
ENST00000334363.14:c.324A>T	ENSP00000334451.9:p.Gln108His
ENST00000400518.5:c.234A>T	ENSP00000383362.1:p.Gln78His
ENST00000400519.6:c.321A>T	ENSP00000383363.1:p.Gln107His
ENST00000400521.6:c.324A>T	ENSP00000383365.1:p.Gln108His
ENST00000400525.6:c.255A>T	ENSP00000383369.3:p.Gln85His
ENST00000474308.5:c.267A>T	ENSP00000485665.1:p.Gln89His
ENST00000491939.6:c.228A>T	ENSP00000485543.1:p.Gln76His
ENST00000496729.2:n.329A>T
ENST00000542719.6:c.36A>T	ENSP00000485128.2:p.Gln12His
NM_001282512.1:c.324A>T	NP_001269441.1:p.Gln108His
NM_006440.4:c.324A>T	NP_006431.2:p.Gln108His
NM_001282512.2:c.324A>T	NP_001269441.1:p.Gln108His
NM_001352300.1:c.321A>T	NP_001339229.1:p.Gln107His
NM_001352301.1:c.234A>T	NP_001339230.1:p.Gln78His
NM_001352302.1:c.36A>T	NP_001339231.1:p.Gln12His
NM_001352303.1:c.228A>T	NP_001339232.1:p.Gln76His
NR_147957.1:n.456A>T
NM_006440.5:c.324A>T MANE Select	NP_006431.2:p.Gln108His
NM_001282512.3:c.324A>T	NP_001269441.1:p.Gln108His
NM_001352300.2:c.321A>T	NP_001339229.1:p.Gln107His
NR_147957.2:n.282A>T
NM_001352301.2:c.234A>T	NP_001339230.1:p.Gln78His
NM_001352302.2:c.36A>T	NP_001339231.1:p.Gln12His
NM_001352303.2:c.228A>T	NP_001339232.1:p.Gln76His