Canonical Allele Identifier: CA513369118

Gene: TXNRD2

Linked Data

• gnomAD v4: 22-19918999-G-T
• MyVariant Identifiers: chr22:g.19906522G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918999G>T , CM000684.2:g.19918999G>T	GRCh38
NC_000022.10:g.19906522G>T , CM000684.1:g.19906522G>T	GRCh37
NC_000022.9:g.18286522G>T	NCBI36
NG_011835.1:g.27838C>A , LRG_417:g.27838C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.235C>A MANE Select	ENSP00000383365.1:p.Arg79=
ENST00000334363.14:c.235C>A	ENSP00000334451.9:p.Arg79=
ENST00000400518.5:c.145C>A	ENSP00000383362.1:p.Arg49=
ENST00000400519.6:c.232C>A	ENSP00000383363.1:p.Arg78=
ENST00000400521.6:c.235C>A	ENSP00000383365.1:p.Arg79=
ENST00000400525.6:c.166C>A	ENSP00000383369.3:p.Arg56=
ENST00000474308.5:c.178C>A	ENSP00000485665.1:p.Arg60=
ENST00000491939.6:c.139C>A	ENSP00000485543.1:p.Arg47=
ENST00000496729.2:n.240C>A
ENST00000542719.6:c.-54C>A	ENSP00000485128.2:n.-54C>A
NM_001282512.1:c.235C>A	NP_001269441.1:p.Arg79=
NM_006440.4:c.235C>A	NP_006431.2:p.Arg79=
NM_001282512.2:c.235C>A	NP_001269441.1:p.Arg79=
NM_001352300.1:c.232C>A	NP_001339229.1:p.Arg78=
NM_001352301.1:c.145C>A	NP_001339230.1:p.Arg49=
NM_001352302.1:c.-54C>A	NP_001339231.1:n.-54C>A
NM_001352303.1:c.139C>A	NP_001339232.1:p.Arg47=
NR_147957.1:n.367C>A
NM_006440.5:c.235C>A MANE Select	NP_006431.2:p.Arg79=
NM_001282512.3:c.235C>A	NP_001269441.1:p.Arg79=
NM_001352300.2:c.232C>A	NP_001339229.1:p.Arg78=
NR_147957.2:n.193C>A
NM_001352301.2:c.145C>A	NP_001339230.1:p.Arg49=
NM_001352302.2:c.-54C>A	NP_001339231.1:n.-54C>A
NM_001352303.2:c.139C>A	NP_001339232.1:p.Arg47=