Canonical Allele Identifier: CA513365161

Gene: TXNRD2

Linked Data

• gnomAD v4: 22-19895447-C-T
• MyVariant Identifiers: chr22:g.19882970C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895447C>T , CM000684.2:g.19895447C>T	GRCh38
NC_000022.10:g.19882970C>T , CM000684.1:g.19882970C>T	GRCh37
NC_000022.9:g.18262970C>T	NCBI36
NG_011835.1:g.51390G>A , LRG_417:g.51390G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.909G>A MANE Select	ENSP00000383365.1:p.Lys303=
ENST00000334363.14:c.909G>A	ENSP00000334451.9:p.Lys303=
ENST00000400518.5:c.819G>A	ENSP00000383362.1:p.Lys273=
ENST00000400519.6:c.906G>A	ENSP00000383363.1:p.Lys302=
ENST00000400521.6:c.909G>A	ENSP00000383365.1:p.Lys303=
ENST00000400525.6:c.840G>A	ENSP00000383369.3:p.Lys280=
ENST00000474308.5:c.852G>A	ENSP00000485665.1:p.Lys284=
ENST00000475995.3:c.406G>A
ENST00000491939.6:c.813G>A	ENSP00000485543.1:p.Lys271=
ENST00000494454.5:n.983G>A
ENST00000542719.6:c.621G>A	ENSP00000485128.2:p.Lys207=
ENST00000634537.1:c.138G>A	ENSP00000489208.1:p.Lys46=
ENST00000635155.1:n.495G>A
NM_001282512.1:c.909G>A	NP_001269441.1:p.Lys303=
NM_006440.4:c.909G>A	NP_006431.2:p.Lys303=
NM_001282512.2:c.909G>A	NP_001269441.1:p.Lys303=
NM_001352300.1:c.906G>A	NP_001339229.1:p.Lys302=
NM_001352301.1:c.819G>A	NP_001339230.1:p.Lys273=
NM_001352302.1:c.621G>A	NP_001339231.1:p.Lys207=
NM_001352303.1:c.813G>A	NP_001339232.1:p.Lys271=
NR_147957.1:n.1041G>A
NM_006440.5:c.909G>A MANE Select	NP_006431.2:p.Lys303=
NM_001282512.3:c.909G>A	NP_001269441.1:p.Lys303=
NM_001352300.2:c.906G>A	NP_001339229.1:p.Lys302=
NR_147957.2:n.867G>A
NM_001352301.2:c.819G>A	NP_001339230.1:p.Lys273=
NM_001352302.2:c.621G>A	NP_001339231.1:p.Lys207=
NM_001352303.2:c.813G>A	NP_001339232.1:p.Lys271=