Canonical Allele Identifier: CA410686759

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19883088A>G (hg19) ; chr22:g.19895565A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895565A>G , CM000684.2:g.19895565A>G	GRCh38
NC_000022.10:g.19883088A>G , CM000684.1:g.19883088A>G	GRCh37
NC_000022.9:g.18263088A>G	NCBI36
NG_011835.1:g.51272T>C , LRG_417:g.51272T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.791T>C MANE Select	ENSP00000383365.1:p.Val264Ala
ENST00000334363.14:c.791T>C	ENSP00000334451.9:p.Val264Ala
ENST00000400518.5:c.701T>C	ENSP00000383362.1:p.Val234Ala
ENST00000400519.6:c.788T>C	ENSP00000383363.1:p.Val263Ala
ENST00000400521.6:c.791T>C	ENSP00000383365.1:p.Val264Ala
ENST00000400525.6:c.722T>C	ENSP00000383369.3:p.Val241Ala
ENST00000474308.5:c.734T>C	ENSP00000485665.1:p.Val245Ala
ENST00000475995.3:c.288T>C
ENST00000491939.6:c.695T>C	ENSP00000485543.1:p.Val232Ala
ENST00000494454.5:n.865T>C
ENST00000542719.6:c.503T>C	ENSP00000485128.2:p.Val168Ala
ENST00000634537.1:c.20T>C	ENSP00000489208.1:p.Val7Ala
ENST00000635155.1:n.377T>C
NM_001282512.1:c.791T>C	NP_001269441.1:p.Val264Ala
NM_006440.4:c.791T>C	NP_006431.2:p.Val264Ala
NM_001282512.2:c.791T>C	NP_001269441.1:p.Val264Ala
NM_001352300.1:c.788T>C	NP_001339229.1:p.Val263Ala
NM_001352301.1:c.701T>C	NP_001339230.1:p.Val234Ala
NM_001352302.1:c.503T>C	NP_001339231.1:p.Val168Ala
NM_001352303.1:c.695T>C	NP_001339232.1:p.Val232Ala
NR_147957.1:n.923T>C
NM_006440.5:c.791T>C MANE Select	NP_006431.2:p.Val264Ala
NM_001282512.3:c.791T>C	NP_001269441.1:p.Val264Ala
NM_001352300.2:c.788T>C	NP_001339229.1:p.Val263Ala
NR_147957.2:n.749T>C
NM_001352301.2:c.701T>C	NP_001339230.1:p.Val234Ala
NM_001352302.2:c.503T>C	NP_001339231.1:p.Val168Ala
NM_001352303.2:c.695T>C	NP_001339232.1:p.Val232Ala