Canonical Allele Identifier: CA513365152

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19882952A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895429A>G , CM000684.2:g.19895429A>G	GRCh38
NC_000022.10:g.19882952A>G , CM000684.1:g.19882952A>G	GRCh37
NC_000022.9:g.18262952A>G	NCBI36
NG_011835.1:g.51408T>C , LRG_417:g.51408T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.927T>C MANE Select	ENSP00000383365.1:p.Phe309=
ENST00000334363.14:c.927T>C	ENSP00000334451.9:p.Phe309=
ENST00000400518.5:c.837T>C	ENSP00000383362.1:p.Phe279=
ENST00000400519.6:c.924T>C	ENSP00000383363.1:p.Phe308=
ENST00000400521.6:c.927T>C	ENSP00000383365.1:p.Phe309=
ENST00000400525.6:c.858T>C	ENSP00000383369.3:p.Phe286=
ENST00000474308.5:c.870T>C	ENSP00000485665.1:p.Phe290=
ENST00000475995.3:c.424T>C
ENST00000491939.6:c.831T>C	ENSP00000485543.1:p.Phe277=
ENST00000494454.5:n.1001T>C
ENST00000542719.6:c.639T>C	ENSP00000485128.2:p.Phe213=
ENST00000634537.1:c.156T>C	ENSP00000489208.1:p.Phe52=
ENST00000635155.1:n.513T>C
NM_001282512.1:c.927T>C	NP_001269441.1:p.Phe309=
NM_006440.4:c.927T>C	NP_006431.2:p.Phe309=
NM_001282512.2:c.927T>C	NP_001269441.1:p.Phe309=
NM_001352300.1:c.924T>C	NP_001339229.1:p.Phe308=
NM_001352301.1:c.837T>C	NP_001339230.1:p.Phe279=
NM_001352302.1:c.639T>C	NP_001339231.1:p.Phe213=
NM_001352303.1:c.831T>C	NP_001339232.1:p.Phe277=
NR_147957.1:n.1059T>C
NM_006440.5:c.927T>C MANE Select	NP_006431.2:p.Phe309=
NM_001282512.3:c.927T>C	NP_001269441.1:p.Phe309=
NM_001352300.2:c.924T>C	NP_001339229.1:p.Phe308=
NR_147957.2:n.885T>C
NM_001352301.2:c.837T>C	NP_001339230.1:p.Phe279=
NM_001352302.2:c.639T>C	NP_001339231.1:p.Phe213=
NM_001352303.2:c.831T>C	NP_001339232.1:p.Phe277=