Canonical Allele Identifier: CA513365163

Gene: TXNRD2

Linked Data

• gnomAD v4: 22-19895450-G-C
• MyVariant Identifiers: chr22:g.19882973G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895450G>C , CM000684.2:g.19895450G>C	GRCh38
NC_000022.10:g.19882973G>C , CM000684.1:g.19882973G>C	GRCh37
NC_000022.9:g.18262973G>C	NCBI36
NG_011835.1:g.51387C>G , LRG_417:g.51387C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.906C>G MANE Select	ENSP00000383365.1:p.Gly302=
ENST00000334363.14:c.906C>G	ENSP00000334451.9:p.Gly302=
ENST00000400518.5:c.816C>G	ENSP00000383362.1:p.Gly272=
ENST00000400519.6:c.903C>G	ENSP00000383363.1:p.Gly301=
ENST00000400521.6:c.906C>G	ENSP00000383365.1:p.Gly302=
ENST00000400525.6:c.837C>G	ENSP00000383369.3:p.Gly279=
ENST00000474308.5:c.849C>G	ENSP00000485665.1:p.Gly283=
ENST00000475995.3:c.403C>G
ENST00000491939.6:c.810C>G	ENSP00000485543.1:p.Gly270=
ENST00000494454.5:n.980C>G
ENST00000542719.6:c.618C>G	ENSP00000485128.2:p.Gly206=
ENST00000634537.1:c.135C>G	ENSP00000489208.1:p.Gly45=
ENST00000635155.1:n.492C>G
NM_001282512.1:c.906C>G	NP_001269441.1:p.Gly302=
NM_006440.4:c.906C>G	NP_006431.2:p.Gly302=
NM_001282512.2:c.906C>G	NP_001269441.1:p.Gly302=
NM_001352300.1:c.903C>G	NP_001339229.1:p.Gly301=
NM_001352301.1:c.816C>G	NP_001339230.1:p.Gly272=
NM_001352302.1:c.618C>G	NP_001339231.1:p.Gly206=
NM_001352303.1:c.810C>G	NP_001339232.1:p.Gly270=
NR_147957.1:n.1038C>G
NM_006440.5:c.906C>G MANE Select	NP_006431.2:p.Gly302=
NM_001282512.3:c.906C>G	NP_001269441.1:p.Gly302=
NM_001352300.2:c.903C>G	NP_001339229.1:p.Gly301=
NR_147957.2:n.864C>G
NM_001352301.2:c.816C>G	NP_001339230.1:p.Gly272=
NM_001352302.2:c.618C>G	NP_001339231.1:p.Gly206=
NM_001352303.2:c.810C>G	NP_001339232.1:p.Gly270=