Canonical Allele Identifier: CA322099008

Gene: TXNRD2

Linked Data

• dbSNP Id: rs1045022447
• MyVariant Identifiers: chr22:g.19883028A>G (hg19) ; chr22:g.19895505A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895505A>G , CM000684.2:g.19895505A>G	GRCh38
NC_000022.10:g.19883028A>G , CM000684.1:g.19883028A>G	GRCh37
NC_000022.9:g.18263028A>G	NCBI36
NG_011835.1:g.51332T>C , LRG_417:g.51332T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.851T>C MANE Select	ENSP00000383365.1:p.Val284Ala
ENST00000334363.14:c.851T>C	ENSP00000334451.9:p.Val284Ala
ENST00000400518.5:c.761T>C	ENSP00000383362.1:p.Val254Ala
ENST00000400519.6:c.848T>C	ENSP00000383363.1:p.Val283Ala
ENST00000400521.6:c.851T>C	ENSP00000383365.1:p.Val284Ala
ENST00000400525.6:c.782T>C	ENSP00000383369.3:p.Val261Ala
ENST00000474308.5:c.794T>C	ENSP00000485665.1:p.Val265Ala
ENST00000475995.3:c.348T>C
ENST00000491939.6:c.755T>C	ENSP00000485543.1:p.Val252Ala
ENST00000494454.5:n.925T>C
ENST00000542719.6:c.563T>C	ENSP00000485128.2:p.Val188Ala
ENST00000634537.1:c.80T>C	ENSP00000489208.1:p.Val27Ala
ENST00000635155.1:n.437T>C
NM_001282512.1:c.851T>C	NP_001269441.1:p.Val284Ala
NM_006440.4:c.851T>C	NP_006431.2:p.Val284Ala
NM_001282512.2:c.851T>C	NP_001269441.1:p.Val284Ala
NM_001352300.1:c.848T>C	NP_001339229.1:p.Val283Ala
NM_001352301.1:c.761T>C	NP_001339230.1:p.Val254Ala
NM_001352302.1:c.563T>C	NP_001339231.1:p.Val188Ala
NM_001352303.1:c.755T>C	NP_001339232.1:p.Val252Ala
NR_147957.1:n.983T>C
NM_006440.5:c.851T>C MANE Select	NP_006431.2:p.Val284Ala
NM_001282512.3:c.851T>C	NP_001269441.1:p.Val284Ala
NM_001352300.2:c.848T>C	NP_001339229.1:p.Val283Ala
NR_147957.2:n.809T>C
NM_001352301.2:c.761T>C	NP_001339230.1:p.Val254Ala
NM_001352302.2:c.563T>C	NP_001339231.1:p.Val188Ala
NM_001352303.2:c.755T>C	NP_001339232.1:p.Val252Ala