Canonical Allele Identifier: CA410686664

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19883043C>A (hg19) ; chr22:g.19895520C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895520C>A , CM000684.2:g.19895520C>A	GRCh38
NC_000022.10:g.19883043C>A , CM000684.1:g.19883043C>A	GRCh37
NC_000022.9:g.18263043C>A	NCBI36
NG_011835.1:g.51317G>T , LRG_417:g.51317G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.836G>T MANE Select	ENSP00000383365.1:p.Cys279Phe
ENST00000334363.14:c.836G>T	ENSP00000334451.9:p.Cys279Phe
ENST00000400518.5:c.746G>T	ENSP00000383362.1:p.Cys249Phe
ENST00000400519.6:c.833G>T	ENSP00000383363.1:p.Cys278Phe
ENST00000400521.6:c.836G>T	ENSP00000383365.1:p.Cys279Phe
ENST00000400525.6:c.767G>T	ENSP00000383369.3:p.Cys256Phe
ENST00000474308.5:c.779G>T	ENSP00000485665.1:p.Cys260Phe
ENST00000475995.3:c.333G>T
ENST00000491939.6:c.740G>T	ENSP00000485543.1:p.Cys247Phe
ENST00000494454.5:n.910G>T
ENST00000542719.6:c.548G>T	ENSP00000485128.2:p.Cys183Phe
ENST00000634537.1:c.65G>T	ENSP00000489208.1:p.Cys22Phe
ENST00000635155.1:n.422G>T
NM_001282512.1:c.836G>T	NP_001269441.1:p.Cys279Phe
NM_006440.4:c.836G>T	NP_006431.2:p.Cys279Phe
NM_001282512.2:c.836G>T	NP_001269441.1:p.Cys279Phe
NM_001352300.1:c.833G>T	NP_001339229.1:p.Cys278Phe
NM_001352301.1:c.746G>T	NP_001339230.1:p.Cys249Phe
NM_001352302.1:c.548G>T	NP_001339231.1:p.Cys183Phe
NM_001352303.1:c.740G>T	NP_001339232.1:p.Cys247Phe
NR_147957.1:n.968G>T
NM_006440.5:c.836G>T MANE Select	NP_006431.2:p.Cys279Phe
NM_001282512.3:c.836G>T	NP_001269441.1:p.Cys279Phe
NM_001352300.2:c.833G>T	NP_001339229.1:p.Cys278Phe
NR_147957.2:n.794G>T
NM_001352301.2:c.746G>T	NP_001339230.1:p.Cys249Phe
NM_001352302.2:c.548G>T	NP_001339231.1:p.Cys183Phe
NM_001352303.2:c.740G>T	NP_001339232.1:p.Cys247Phe