Canonical Allele Identifier: CA513365299

Gene: TXNRD2

Linked Data

• gnomAD v4: 22-19895510-C-G
• MyVariant Identifiers: chr22:g.19883033C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895510C>G , CM000684.2:g.19895510C>G	GRCh38
NC_000022.10:g.19883033C>G , CM000684.1:g.19883033C>G	GRCh37
NC_000022.9:g.18263033C>G	NCBI36
NG_011835.1:g.51327G>C , LRG_417:g.51327G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.846G>C MANE Select	ENSP00000383365.1:p.Ser282=
ENST00000334363.14:c.846G>C	ENSP00000334451.9:p.Ser282=
ENST00000400518.5:c.756G>C	ENSP00000383362.1:p.Ser252=
ENST00000400519.6:c.843G>C	ENSP00000383363.1:p.Ser281=
ENST00000400521.6:c.846G>C	ENSP00000383365.1:p.Ser282=
ENST00000400525.6:c.777G>C	ENSP00000383369.3:p.Ser259=
ENST00000474308.5:c.789G>C	ENSP00000485665.1:p.Ser263=
ENST00000475995.3:c.343G>C
ENST00000491939.6:c.750G>C	ENSP00000485543.1:p.Ser250=
ENST00000494454.5:n.920G>C
ENST00000542719.6:c.558G>C	ENSP00000485128.2:p.Ser186=
ENST00000634537.1:c.75G>C	ENSP00000489208.1:p.Ser25=
ENST00000635155.1:n.432G>C
NM_001282512.1:c.846G>C	NP_001269441.1:p.Ser282=
NM_006440.4:c.846G>C	NP_006431.2:p.Ser282=
NM_001282512.2:c.846G>C	NP_001269441.1:p.Ser282=
NM_001352300.1:c.843G>C	NP_001339229.1:p.Ser281=
NM_001352301.1:c.756G>C	NP_001339230.1:p.Ser252=
NM_001352302.1:c.558G>C	NP_001339231.1:p.Ser186=
NM_001352303.1:c.750G>C	NP_001339232.1:p.Ser250=
NR_147957.1:n.978G>C
NM_006440.5:c.846G>C MANE Select	NP_006431.2:p.Ser282=
NM_001282512.3:c.846G>C	NP_001269441.1:p.Ser282=
NM_001352300.2:c.843G>C	NP_001339229.1:p.Ser281=
NR_147957.2:n.804G>C
NM_001352301.2:c.756G>C	NP_001339230.1:p.Ser252=
NM_001352302.2:c.558G>C	NP_001339231.1:p.Ser186=
NM_001352303.2:c.750G>C	NP_001339232.1:p.Ser250=