Canonical Allele Identifier: CA513369098

Gene: TXNRD2

Linked Data

• gnomAD v4: 22-19918964-G-C
• MyVariant Identifiers: chr22:g.19906487G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918964G>C , CM000684.2:g.19918964G>C	GRCh38
NC_000022.10:g.19906487G>C , CM000684.1:g.19906487G>C	GRCh37
NC_000022.9:g.18286487G>C	NCBI36
NG_011835.1:g.27873C>G , LRG_417:g.27873C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.270C>G MANE Select	ENSP00000383365.1:p.Gly90=
ENST00000334363.14:c.270C>G	ENSP00000334451.9:p.Gly90=
ENST00000400518.5:c.180C>G	ENSP00000383362.1:p.Gly60=
ENST00000400519.6:c.267C>G	ENSP00000383363.1:p.Gly89=
ENST00000400521.6:c.270C>G	ENSP00000383365.1:p.Gly90=
ENST00000400525.6:c.201C>G	ENSP00000383369.3:p.Gly67=
ENST00000474308.5:c.213C>G	ENSP00000485665.1:p.Gly71=
ENST00000491939.6:c.174C>G	ENSP00000485543.1:p.Gly58=
ENST00000496729.2:n.275C>G
ENST00000542719.6:c.-19C>G	ENSP00000485128.2:n.-19C>G
NM_001282512.1:c.270C>G	NP_001269441.1:p.Gly90=
NM_006440.4:c.270C>G	NP_006431.2:p.Gly90=
NM_001282512.2:c.270C>G	NP_001269441.1:p.Gly90=
NM_001352300.1:c.267C>G	NP_001339229.1:p.Gly89=
NM_001352301.1:c.180C>G	NP_001339230.1:p.Gly60=
NM_001352302.1:c.-19C>G	NP_001339231.1:n.-19C>G
NM_001352303.1:c.174C>G	NP_001339232.1:p.Gly58=
NR_147957.1:n.402C>G
NM_006440.5:c.270C>G MANE Select	NP_006431.2:p.Gly90=
NM_001282512.3:c.270C>G	NP_001269441.1:p.Gly90=
NM_001352300.2:c.267C>G	NP_001339229.1:p.Gly89=
NR_147957.2:n.228C>G
NM_001352301.2:c.180C>G	NP_001339230.1:p.Gly60=
NM_001352302.2:c.-19C>G	NP_001339231.1:n.-19C>G
NM_001352303.2:c.174C>G	NP_001339232.1:p.Gly58=